Explanation of basic terms of clinical examination and sorting out major questions

Glossary:

1. Serum The liquid separated from the natural coagulation of isolated blood

2. Anticoagulants or anticoagulant substances Substances that inhibit blood clotting

3. Basic dyes The colored part is cationic, which can combine with acidic substances in cells, such as DNA, RNA, etc., and is mainly used for staining the nucleus

4. Red blood cell count (RBC) , combined with hemoglobin and hematocrit, is often used as one of the main indicators for diagnosing anemia, polycythemia vera and polycythemia

5. Hemoglobin (Hb or HGB) is a binding protein containing pigment prosthetic groups synthesized in human nucleated erythrocytes and reticulocytes, and is a transport protein in erythrocytes

6. Reticulocytes (RET) are transitional cells between late immature red blood cells and mature red blood cells, slightly larger than mature red blood cells

7. Erythrocyte sedimentation rate (ESR) Under specified conditions, the natural sinking rate of red blood cells in anticoagulated whole blood in vitro

8. Uneven size of neutrophils The size of neutrophils varies greatly, and the heterogeneity increases

9. Toxic granules In the case of severe infection and extensive burns, neutrophils appear in the cytoplasm of neutrophils, which are thicker than normal neutrophils, with different sizes and uneven distribution of purple-black or dark purple-brown granules

10. Left shift of nucleus Increased neutrophils in peripheral blood or metamyelocytes, myelocytes and even promyelocytes

11. Nucleus shifted to the right. Neutrophils in the peripheral blood were increased, and the number of neutrophils above 5 lobes was >3%

12. Under the stimulation of virus, protozoan infection, drug reaction, connective tissue disease, stress state or allergen and other factors, atypical lymphocytes proliferate and undergo morphological changes. Increased alkalinity, nucleoblastification

13. Degeneration Cell body enlargement, blurred structure, unclear edges, nuclear pyknosis, nuclear swelling, nuclear dissolution, etc., are common in aging and diseased cells

14. Basophilic stippling erythrocytes are immature erythrocytes, granules formed by residual nucleic acid denaturation and aggregation in the cytoplasm, after staining with basic dyes, deeply stained granules can be seen in the cells

15. Blood type and blood type system Blood type: the genetic traits of various blood component antigens, which is one of the main characteristics of blood Blood type system: a group of antigens produced by a single gene or alleles of multiple closely linked loci

16. Cross-matching blood test Based on blood type identification, it is a test to further check whether the blood of the recipient and the donor contains incompatible antigens and antibody components

17. ABO blood group identification The ABO blood group antibody is mainly IgM, which belongs to complete antibody. The molecular chain of IgM antibody is longer, which can overcome the repulsive force on the surface of red blood cells. At the same time, its relative molecular mass is relatively large, and it can specifically bind to the corresponding antigen in normal saline to cause agglutination phenomenon visible to the naked eye.

18. Red blood cell histogram The normal red blood cell histogram is a unimodal curve with approximately normal distribution, usually in the range of 36~360fl, the abscissa indicates the volume of red blood cells, and the ordinate indicates the probability of red blood cells with different volumes

19. Platelet histogram Normal platelet histogram is a unimodal smooth curve with skewed distribution, usually in the range of 2~30fl, mainly concentrated at 2~15fl

20. The laser light scattering method injects the diluted, stained and spheroidized cell suspension into the center of the sheath flow, and the single cells are neatly arranged along the two streams of the suspension and the sheath flow, and pass through the quartz capillary at a constant flow rate, that is, the fluid dynamics Learning Focus Technology

21. Glomerular proteinuria After the glomerular filtration membrane is damaged by inflammation, immunity, metabolism and other factors, the pore size of the filtration membrane increases, breaks and the electrostatic barrier function is weakened, and plasma proteins, especially albumin, are filtered out. Proteinuria due to proximal tubular reabsorptive capacity

22. Chyluria is due to the rupture of lymphatic vessels in the urinary system or the obstruction of deep lymphatic vessels, causing chyle fluid or lymph fluid to enter the urine, and the urine is milky white and turbid

23. Microscopic hematuria No red in the urine appearance, red blood cells > 3/HP under the centrifugal urine microscope

24.

25. Renal tubular proteinuria When the renal tubules are infected, poisoned, damaged or secondary to glomerular diseases, the reabsorption capacity is reduced or inhibited, resulting in proteinuria mainly composed of proteins with relatively small molecular weights

26. Tissue proteinuria is derived from the protein produced by renal tubule metabolism, tissue destruction and decomposition, inflammation or drug-stimulated urinary system secretion, which enters the urine to form proteinuria

27. Urine specific gravity The ratio of urine to the weight of the same volume of pure water at 4°C is an indicator of the concentration of solutes contained in urine

28. Urine osmolarity is the total number of osmotically active solute particles in urine, which has nothing to do with particle size and charge. Macromolecular substances such as protein and glucose have little influence on it, and can accurately reflect the concentration and dilution functions of the kidney.

29. Urine centrifugal staining microscopy is used to identify pathological formed elements and improve the contrast of white blood cells, flash cells, epithelial cells, casts, crystals, bacteria and fungi, which is helpful to identify cells and casts, especially to prevent missed detection Clear casts that can be examined microscopically after staining

30. Transparent cast , also known as glass cast, is mainly composed of TH protein, also contains albumin and sodium chloride, is colorless and transparent, and can dissolve and disappear in alkaline urine

31. Calcium oxalate crystals Colorless square shimmering octahedron or envelope-like, with two diagonals intersecting each other, sometimes diamond-shaped, occasionally dumbbell-shaped or pie-shaped

32. Urine Formed Components Components that are excreted through urine and can be detected under a microscope

33. Metabolic diabetes is caused by hyperglycemia caused by abnormal secretion of endocrine hormones and glucose metabolism

34. Waxy casts are derived from granular casts, or casts gradually formed after amyloidogenic epithelial cells are lysed, and may also be evolved from hyaline casts that stay in the renal tubules for a long time

35. Occult Blood Test (FOBT) A test to check for fecal occult blood

36. Intestinal flora disorder The ratio of Gram-positive cocci to Gram-negative bacilli in feces is >1:10, normal flora decreases or even disappears, and staphylococci or fungi increase significantly

37. Sperm motility rate Directly observe the ratio of motile sperm to the total number of sperm under a microscope

38. Sperm motility The ability of sperm to move forward

39. Spermatogenic cells are immature germ cells, which refer to hypoplastic germ cells at various stages, such as spermatogonia, primary spermatocytes, secondary spermatocytes and hypoplastic sperm cells

40. Sperm count One refers to counting the number of sperm in a unit volume, that is, sperm concentration. The other is the total number of sperm, that is, the absolute number of sperm discharged at a single time (sperm concentration × volume of semen this time)

41. Prostatic fluid An opaque, light milky liquid secreted by the prostate gland, which is an important part of semen

42. Phosphatidylcholine body The main component is phosphatidylcholine, which is round or oval, with strong refraction, uneven size, similar to platelets, but slightly larger, so it should be distinguished from platelets when observed

43. Vaginal discharge The fluid secreted by the female reproductive system is mainly composed of secretions from the vaginal mucosa, cervical glands, Bartholin glands and endometrium, commonly known as leucorrhea

44. Cerebrospinal fluid is a colorless and transparent liquid present in the ventricles, subarachnoid space, and central canal of the spinal cord

45. Mucin typing test is a simple mucin screening test that can roughly distinguish inflammatory effusions from non-inflammatory effusions

46. ​​Bloody exudate is generally red, dark red or jam-colored, and is common in trauma, malignant tumor, tuberculous effusion and pulmonary infarction

47. Transudate Fluid in body cavity caused by heart failure, hypoproteinemia, etc. Non-inflammatory effusion accumulated in tissue space or body cavity

48. Exudate Fluid exuded during inflammation Inflammatory effusion caused by local tissue inflammation

49. Carcinoembryonic antigen alpha-fetoprotein sugar chain antigen serosal effusion tumor marker

Answer questions:

1. Commonly used anticoagulants and anticoagulant principles for blood samples

anticoagulant

Principle of anticoagulation

Ethylenediaminetetraacetate (EDTA)

Combine with Ca2+ in the blood to form a chelate, interrupting the coagulation process

sodium citrate

Binds to Ca2+ in blood

heparin

Strengthened antithrombin inactivates serine proteases, preventing thrombin formation

Oxalate

Combine with Ca2+ in blood to form calcium oxalate precipitate

2. Blood collection method of skin blood collection method

u Gently massage the blood collection site (the inner side of the ring finger of the left hand or the earlobe) to make the local tissue congest naturally

u Disinfect the skin, after it dries, pinch both sides of the blood collection site tightly

u Hold a disposable sterilized blood collection needle in your right hand and insert it quickly (the depth is preferably 2-3mm), and the blood will flow out by itself or after a little squeezing. Because the first drop of blood is mixed with tissue fluid, it is generally discarded, or it is decided whether to use it according to the requirements of the test items.

u After the blood collection, press the blood collection site with a sterile dry cotton swab to stop the bleeding

3. Precautions for skin blood collection method

u Pay attention to strict disinfection and biosafety precautions when collecting blood, and the blood collection needle is for one-time use

u Squeeze slightly when taking blood, but do not use too much force to avoid mixing too much tissue fluid into the blood

u Blood collection should be done quickly to prevent coagulation of the outflowing blood

u When multiple routine examinations are performed manually, the order of blood sample collection is platelet count, red blood cell count, hemoglobin determination, white blood cell count and white blood cell differential count

4. Blood collection method of soft-connected two-way blood collection needle

u Tie the cuff on the upper end of the puncture point, and ask the subject to clench his fist to make the vein full and exposed

u Pull out the sheath of the blood collection puncture needle, fix the blood vessel with the left hand, hold the puncture needle with the thumb and index finger of the right hand, pierce the skin along the direction of the vein so that the needle and the skin form an angle of 30°, and then puncture forward (the needle forms an angle of 5° with the skin) Vein wall enters venous cavity

u After blood returns, insert the rubber plug puncture needle (the other end of the two-way needle is covered with soft rubber latex) directly into the center of the rubber head cover of the negative pressure blood collection tube, the blood will be automatically sucked into the blood collection tube, and the cuff will be loosened at the same time

u If multiple tubes of blood samples are required, pull out the puncture needle and then puncture another blood collection tube

u After blood collection, ask the subject to loosen his clenched fist, press the puncture point with a sterile dry cotton swab, pull out the puncture needle, and continue to press the puncture point for several minutes

5. Clinical significance of physiological increase in red blood cells

u hypoxia, such as newborns (35% increase), mountain dwellers (14% increase), mountaineers, strenuous exercise and manual laborers

u Increased androgen, such as adult males are higher than females

u Increased adrenal cortex hormones, such as mood swings (emotional impulse, excitement, fear)

u long-term heavy smoking

u Venous compression time > 2 minutes (10% increase)

u Capillary blood is higher than venous blood (increased by 10%~15%)

u Intra-day difference, as the number of red blood cells is the highest at 7 am in one day

u Drug effects, such as the application of epinephrine, glucocorticoid drugs

6. Briefly explain the cause of pathological increase in red blood cells

increase

reason

Relative hypertrophy (decreased blood volume)

Vomiting, high fever, diarrhea, polyuria, sweating, extensive burns

Absolute increase

secondary increase

1. Tissue hypoxia: severe chronic cardiopulmonary disease, cyanotic congenital heart disease

2. Compensatory increase in erythropoietin (EPO): abnormal hemoglobinopathies

3. Uncompensated increase of erythropoietin (EPO): kidney cancer, liver cancer, uterine fibroids, ovarian cancer, renal embryonic tumor, hydronephrosis, polycystic kidney and kidney transplantation

primary hyperplasia

polycythemia vera

7. Clinical significance of reticulocyte count

u Evaluate bone marrow proliferative ability and judge the type of anemia

u Evaluate curative effect

u Monitoring of radiotherapy and chemotherapy

u drug effects

8. Quality assurance items and evaluation of blood smear preparation

project

evaluate

glass slide

Keep it neutral, clean and non-greasy

Preparation of blood smear

1. The "standard" of a good blood smear is that the blood film gradually transitions from thick to thin. The thickness should be appropriate, the head, body, and tail should be distinct, evenly distributed, with gaps on both sides, and neat edges

2. The thickness and length of the blood film are related to the size of the serum, the angle between the slide and the slide, the speed of the slide and the hematocrit (HCT). The blood drop is large and the angle is large. If the film is pushed fast, the blood film will growl; otherwise, the blood film will be thin.

3. When the HCT is increased, the blood viscosity is high, and it is advisable to keep a smaller angle to obtain a satisfactory blood smear; on the contrary, when the HCT is lower than normal, the blood is thinner, and a larger angle and a faster pusher should be used Only at high speed can a satisfactory blood smear be obtained

dyeing

Blood smears should be stained within 1 hour, or fixed with anhydrous methanol and stained within 1 hour

9. The clinical significance of pathological increased ESR

disease

clinical significance

tissue damage

After severe trauma and major surgery, serum acute phase reactive protein increases rapidly 3-4 days after myocardial infarction

malignant tumor

Associated with tumor necrosis, increased fibrinogen, infection, and anemia

inflammatory disease

Acute bacterial infection (rapid increase in acute phase reactive proteins)

Active rheumatic disease (increased antigen-antibody complexes)

Active tuberculosis, active rheumatic fever (fibrinogen significantly increased)

HIV infection (positive serum markers with increased erythrocyte sedimentation rate is an early predictor of AIDS)

autoimmune disease

Connective tissue disease, ESR has similar sensitivity to C-reactive protein, rheumatoid factor, antinuclear antibody, etc.

Hyperglobulinemia

Multiple myeloma, macroglobulinemia, systemic lupus erythematosus, liver cirrhosis, chronic nephritis,

Increased immunoglobulin

Hypercholesterolemia

Atherosclerosis, diabetes mellitus, myxedema, primary familial hypercholesterolemia

other

Degenerative disease, giant cell arteritis, polymyoma rheumatica

10. Factors affecting the determination of erythrocyte sedimentation rate

Variety

factor

evaluate

speed up

Plasma factor

Fibrinogen, gamma globulins and abnormal clonal immunoglobulins, alpha and beta globulins, elevated cholesterol and triglycerides

red blood cell factor

Large red blood cells are easy to form a thread, which accelerates the erythrocyte sedimentation rate; anemia of various causes

infection factor

Certain viruses, bacteria, drugs, metabolites, and abnormal antibodies neutralize the negative charges on the cell surface

drug factors

Glucose, polyvinylpyrrolidone, gelatin, penicillamine, oral contraceptives, methyldopa, dextran, procainamide, theophylline, vitamin A

Specimen and Physical Condition

Specimen hemolysis, erythrocyte sedimentation tube tilted, temperature too high

slow down

Plasma factor

Increases in albumin, glycoprotein, and phosphatidylcholine inhibit the formation of erythrocyte strings

red blood cell factor

Increased number, uneven size, or increased spherical and sickle cells, which is not conducive to the formation of cords

physical conditions

The erythrocyte sedimentation tube is not clean or the blood column contains air bubbles, and the temperature is too low

drug factors

aspirin, cortisone, quinine

11. Causes of increased reactivity of white blood cells (neutrophils)

category

reason

acute infection

Bacterial, certain viral, fungal, spirochete, rickettsial, and parasitic infections (most common)

inflammation

Rheumatoid arthritis, rheumatic fever, bronchitis, nephritis, pyelonephritis, colitis, pancreatitis, thyroiditis, dermatitis

tissue damage

Severe trauma, major surgery, extensive burns, acute myocardial infarction

blood cell destruction

severe intravascular hemolysis

acute blood loss

Gastrointestinal bleeding, spleen rupture, rupture of ectopic pregnancy

malignant tumor

Non-hematopoietic malignancies, especially gastrointestinal malignancies (liver cancer, gastric cancer) and lung cancer

acute poisoning

Metabolic, chemical, drug, biotoxin, etc. intoxication (associated with increased chemokines)

12. According to the dynamic characteristics of granulocytes, briefly describe the distribution, cell pool and cell types of granulocytes

distributed

cell pool

cell type

Dynamic characteristics

marrow

split pool

Raw grains ~ middle and young grains

With the ability to divide, one myeloblast can proliferate into 16-32 metamyelocytes after 3-5 divisions

marrow

mature pond

late granules and rods

Without the ability to divide, after 3 to 5 days, it will gradually mature

marrow

storage pool

Rod and lobed nuclei

Stay for 3 to 5 days, the amount is about 5 to 20 times that of peripheral blood. The maturation time from mesenchyme to lobular granulocyte is about 5-7 days, which can be shortened to 2 days when stimulated

blood

circulation pool

Few rod-shaped nuclei, lobed nuclei

It is 50% of the granulocytes released into the blood from the bone marrow storage pool, and stays for about 10-12 hours with the blood circulation, and the half-life is about 6-7 hours

blood

edge pool

Lobular nucleus

In order to release the other 50% of the granulocytes in the peripheral blood, adhere to the blood vessel wall, exchange with the granulocytes in the circulating pool at any time, and maintain a dynamic balance, and together with the circulating pool are called the total granulocyte pool

tissue or body cavity

tissue intrinsic pool

Lobular nucleus

The granulocytes escape the blood vessel wall and enter the tissue or body cavity, survive for 1 to 4 days, perform defense functions, no longer return to the blood, and are destroyed, cleared or eliminated in the tissue

13. Causes and significance of pathological thrombocytosis and decrease

platelets

reason

clinical significance

reduce

Generate obstacles

Acute leukemia, aplastic anemia, myeloid neoplasm, radiation injury, megaloblastic anemia

too much damage

Idiopathic thrombocytopenic purpura, hypersplenism, systemic lupus erythematosus

consume too much

DIC, thrombotic thrombocytopenic purpura

abnormal distribution

Splenomegaly, blood thinning

Congenital

Neonatal thrombocytopenia, giant platelet syndrome

increase

primary

Chronic myeloid, essential thrombocythemia, polycythemia vera

reactivity

Acute suppurative infection, massive bleeding, acute hemolysis, tumor

other

After surgery, splenectomy

14. Clinical significance of prolonged and shortened prothrombin time (PT)

u extend:

1. Congenital FⅡ, FⅤ, FⅦ, FX deficiency and low (no) fibrinogenemia

2. Acquired coagulation factor deficiency, such as severe liver disease, vitamin K deficiency, primary fibrinolysis

3. There are anticoagulants in the blood circulation, such as oral anticoagulants

u Shorten:

1. Congenital FⅤ hyperplasia

2. Hypercoagulable state and thrombotic disease

3. Drug effects, such as long-term use of contraceptives

15. Clinical significance of determination of fibrinogen (Fg) content

u Fg increased:

1. Infection: toxemia, pneumonia, subacute bacterial endocarditis

2. Aseptic inflammation: nephrotic syndrome, rheumatic fever, rheumatoid arthritis

3. Prethrombotic state and thrombotic diseases: diabetes, acute myocardial infarction

4. Malignant tumor

5. After trauma, burns, surgery, radiation therapy

6. Others: late pregnancy, pregnancy-induced hypertension syndrome

u Fg reduction:

1. Primary fibrinogen reduction or structural abnormality: low or no fibrinogenemia, dysfibrinogenemia

2. Secondary fibrinogen reduction: advanced DIC, hyperfibrinolysis, severe hepatitis and cirrhosis

16. The site where the ABO blood group system antigen exists

u Complete antigen: on the cell membrane of red blood cells, lymphocytes, platelets, epithelial cells, etc.

u Hapten: in various body fluids or secretions except cerebrospinal fluid

17. The clinical significance of Rh blood group identification

u transfusion

Although about 99.6% of Chinese are Rh positive, and there is generally no Rh antibody in the serum of healthy people, in order to ensure the safety of blood transfusion, RhD antigen identification must be done before blood transfusion, and Rh negative blood recipients must be transfused with Rh negative blood

u Discovered hemolytic disease of the newborn

If the maternal blood contains IgG Rh antibodies against fetal red blood cells, IgG antibodies can pass through the placenta and destroy fetal red blood cells, causing hemolytic disease of the newborn. Therefore, identify the Rh blood type of the newborn and the mother and check the incomplete antibody of Rh to facilitate the detection of hemolytic disease of the newborn

18. Clinical significance of cross-matching blood test

u match to a suitable blood source, verify the blood type

Match to a suitable blood source, and further verify whether the blood type identification of the blood recipient and the blood donor is correct, so as to avoid severe hemolysis reaction after blood transfusion caused by wrong blood type identification

u Discover subtypes

For example, some people of A2 subtype contain anti-A1 serum, and when they are matched with A1 red blood cells, agglutination may occur

u found irregular antibodies

Although the ABO blood type is the same, severe hemolytic transfusion reactions can also occur when the Rh or other blood types are different. Even if Rh or other blood types are not identified, blood type incompatibility or immunity between the recipient and the blood donor can be found through cross-matching Antibody

19. Briefly describe the quality assurance in blood analyzer testing

u The quality assurance of blood analyzer test results shall run through the application of clinicians, nurses or test personnel to collect samples, transport personnel to transfer samples, test personnel to receive samples, test, review and confirm, print results, issue reports, and clinical satisfaction. The whole process

u Quality assurance before testing:

1. Qualified inspectors 2. Suitable testing environment 3. Qualified blood analyzer

4. Supporting reagents 5. Qualified test specimens

u Quality assurance during testing:

1. Instrument startup 2. Indoor quality control 3. Specimen detection 4. Instrument cleaning

u Post-test quality assurance:

1. Analysis of results in the laboratory

2. Combined with the clinical situation for correlation analysis

3. Regularly solicit clinical evaluation of test results

4. Record and report test results that are difficult to interpret

20. Detection principle of electrical impedance hematology analyzer

u The blood cells suspended in the electrolyte solution are non-conductive particles relative to the electrolyte solution. When blood cells (or similar particles) with different volumes pass through the counting hole, it can cause changes in the internal and external current or voltage of the small hole, forming a The pulse voltage with the same volume and size can indirectly distinguish the blood cell groups and count them separately. This is the principle of electrical impedance

21. Types of blood cell count errors and ways to reduce them

Type of error

reason

error reduction method

technical error

Improper blood collection site, inaccurate dilution factor, improper filling, uneven mixing of diluted blood, blood coagulation, improper handling and use of equipment, and wrong cell identification

Standardize operation, use equipment correctly, and improve operation skills

instrument error

Equipment (counting plates, coverslips, pipettes) are inaccurate and imprecise

Calibration of various equipment

count field error

Uneven distribution of blood cells in the counting chamber, etc.

Expand cell count range and volume

22. The concept of blood analyzer alarm

There are three main functions of the blood analyzer:

1. Screening and reporting of normal inspection results, at this time, generally no alarm occurs

2. When the technical conditions are mature, approved by the State Food and Drug Administration, and the report is made within the test item rules set by the instrument or laboratory, there may be no alarm. However, in most cases, an alarm is still issued to remind inspectors to pay close attention to the abnormalities that have occurred

3. When the specimen cannot meet the pre-set rules of the laboratory, the instrument will inevitably alarm and must be re-examined.

u The alarm of the test result means that the reliability of the test result directly reported by the instrument to the clinic has been significantly reduced, and the test result report cannot be directly issued to the clinic without re-examination confirmation or effective explanation

23. General requirements for urine specimen collection

project

General requirements

patient request

The patient is in a quiet state, living and eating according to routine

Physiological state

Exercise, sex, menstruation, excessive fasting or eating, drinking, smoking, and posture and position can affect some test results

avoid pollution

1. The patient first washes his hands and cleans the external genitalia, urethral opening and surrounding skin

2. Female patients should especially avoid urine contamination by vaginal secretions or menstrual blood, and male patients should avoid mixing semen

3. To avoid the mixing of chemicals (such as surfactants, disinfectants), feces and other pollutants

collection time

Urine specimens for bacterial culture must be collected in sterile containers prior to treatment with antibiotics to facilitate bacterial growth

special requirements

1. When using urinary catheter specimens or suprapubic puncture urine specimens, the medical staff should first inform the patient and family members of the relevant precautions, and then the medical staff should collect them

2. When collecting infant urine samples, be guided by pediatric medical staff, and use a special urine bag for children to collect samples

24. Erythrocyte casts and their clinical significance

u Red blood cell casts: morphologically intact red blood cells embedded in the matrix of the casts

u Red blood cell casts are caused by glomerular or tubular hemorrhage, which can be seen in acute glomerulonephritis, acute exacerbation of chronic nephritis, renal hemorrhage, acute tubular necrosis, renal transplant rejection, renal vein thrombosis, and malignant hypertension etc., can also be seen with lupus nephritis, subacute endocarditis and IgA nephropathy

25. Hemoglobinuria and its clinical significance

u Hemoglobinuria: Plasma free hemoglobin increases during intravascular hemolysis, exceeding the globin binding capacity (about 1.3g/L). Because of its relatively small molecular weight, it can be filtered out by glomeruli to form hemoglobinuria

u Clinical significance: common in favism, paroxysmal nocturnal hemoglobinuria (PNH) and transfusion reactions of blood group incompatibility, paroxysmal cold hemoglobinuria (PCH), marching hemoglobinuria, immune hemolytic anemia, etc.

Common factors and diseases of intravascular hemolysis are shown in the table below

factor

disease

red blood cell destruction

Heart valve repair surgery, extensive burns, strenuous exercise, rapid marches, severe muscle trauma, and vascular tissue damage

biological factors

Malaria, contained bacillus poisoning

Hemolysis caused by animals and plants

Snake venom, bee venom, poisonous mushroom (xùn)

microvascular hemolytic anemia

DIC

drug effect

Primaquine, acetylsalicylic acid, sulfonamides, phenacetin

immune factors

Thrombotic thrombocytopenic purpura, paroxysmal cold hemoglobinuria, incompatible blood transfusion

26. Under what circumstances is microscopic examination performed during urinalysis

u The doctor asks for microscopic examination

u Patients with renal disease (regardless of initial or follow-up visits) should go directly to standardized microscopic examination

u Abnormal results of any urine physical and chemical examination. Especially dry chemical examination, if one of the four items of red blood cells, white blood cells, protein and nitrite is abnormal, a microscopic examination must be performed, and the results of the microscopic examination shall prevail

27. Detection principle of urine dry chemical method

u The chemical composition of the urine changes the color of the reagent module on the multiple test strip, and the color depth is proportional to the concentration of the chemical composition in the urine. When the test strip enters the colorimetric tank of the urine dry chemistry analyzer, each reagent module is sequentially irradiated by the light source of the instrument and produces different reflected light. Processing, calculate the reflectance of each detection parameter, compare and correct with the standard curve, and finally output the result automatically in a qualitative or semi-quantitative way

The essence of the detection principle of urine dry chemical method is the absorption and reflection of light. The depth of the color of the reagent module has different absorption and reflection of light. The darker the color, the greater the light absorption, the smaller the light reflection, and the smaller the reflectivity;

28. Tube type and forming conditions

u Casts are cylindrical protein aggregates formed by coagulation of proteins, cells and their disintegrated products in renal tubules and collecting ducts

u Tube formation should meet 3 conditions:

1. There are albumin and Tamm-Horsfall protein (TH protein) in the original urine: this is the matrix and the first condition to form the cast, among which TH protein is the most likely to form the core of the cast

2. The ability of renal tubules to concentrate and acidify urine: Concentration can increase the concentration of protein and salts that form casts, while acidification promotes further protein denaturation, aggregation and precipitation

3. The kidney has nephrons that can be used alternately: it is conducive to the formation and excretion of casts, that is, the urine stasis of nephrons in the "resting" state of lesions occurs, and there is enough time to form casts. When the nephrons get Repair and restore function When urinating again, the formed cast can be excreted with urine

29. Clinical significance of renal failure casts

u Renal failure casts are also called broad casts. Renal failure casts indicate serious renal disease. Patients with acute renal failure with polyuria and early rise may have a large number of wide casts in the urine, which will gradually disappear and disappear with the improvement of renal function. Renal failure casts may appear in advanced chronic nephritis with uremia, which often indicates a poor prognosis. Brown broad hemoglobin casts can be seen in the urine of acute renal failure caused by hemolytic reaction after heterozygous blood transfusion. Pigmented myoglobin casts in urine in acute renal failure following renal crush injury or extensive burns

30. Clinical significance of homogeneous red blood cell hematuria

u Mainly increased red blood cells, but no increase or no obvious increase in urine protein.

u found in:

1. Temporary microscopic hematuria: seen in healthy people, especially adolescents after strenuous exercise, rapid march, cold water bath, standing for too long or after heavy physical labor. Women should also pay attention to the pollution of menstrual blood, which should be distinguished through dynamic observation

2. Urinary system diseases: such as urinary system inflammation, tumor, tuberculosis, calculus, trauma, renal transplant rejection, congenital malformation, etc. Hematuria is sometimes the only clinical manifestation of urological malignancies

3. Reproductive system diseases: such as prostatitis, seminal vesiculitis, etc.

4. Others: bleeding disorders caused by various reasons, etc.

31. The clinical significance of red blood cell examination by stool microscope

u In the case of upper gastrointestinal bleeding, due to the digestion of gastric juice, the red blood cells have been destroyed and it is difficult to see them in the feces

u Different numbers of red blood cells may appear in lower gastrointestinal tract inflammation or bleeding, such as dysentery, ulcerative colitis, colon cancer, rectal polyps, hemorrhoids, acute schistosomiasis, etc.

Inflammatory injury and bleeding: white blood cells and red blood cells can exist at the same time

Bacillary dysentery: polydisperse red blood cells with normal morphology and fewer numbers than white blood cells

Amoebic dysentery: Red blood cells are more sticky and broken than white blood cells

32. Morphology and clinical significance of cells (red blood cells) in feces

cell

form

clinical significance

physiological

pathology

leukocyte

(pus cells)

No or occasionally white blood cells, and those with complete morphology are no different from granulocytes in blood

Neutrophils are grayish white, swollen, necrotic, damaged, with incomplete structure, the cytoplasm is full of fine particles, and the nucleus is not clear (ie, pus cells), often appearing in piles

1. Enteritis: leukocytosis is not obvious, generally <15/HP, scattered

2. Bacillary dysentery, ulcerative enteritis: a large number of white blood cells or pus cells appearing in piles, and small phagocytes that swallow foreign bodies can be seen

3. Irritable bowel syndrome, intestinal parasites (especially hookworm disease and amoebic dysentery): there are more eosinophils in the stool, which may be accompanied by Charcot-Leyden crystals

red blood cells

none

Grass-green, slightly refracting disc-shaped, sometimes shrunken due to the pH of the feces

In upper gastrointestinal bleeding, due to the digestion of gastric juice, the red blood cells have been destroyed and are difficult to see in the stool

Inflammation or hemorrhage of the lower gastrointestinal tract may have varying numbers of red blood cells, such as dysentery, ulcerative colitis, colon cancer, rectal polyps, hemorrhoids, acute schistosomiasis, etc.

33. Reference value and clinical significance of fecal occult blood test

u Reference value: Negative

u Clinical significance: FOBT is mainly used for the screening and identification of gastrointestinal bleeding and gastrointestinal tumors

1. Judgment of gastrointestinal bleeding: positive FOBT is seen in gastrointestinal bleeding, gastric mucosal damage caused by drugs (such as taking aspirin, indomethacin, glucocorticoids, etc.), intestinal tuberculosis, Crohn's disease, gastric ulcer, various gastritis, Ulcerative colitis, colon polyps, hookworm disease, malignant tumors of the digestive tract, etc.

2. Differentiation between peptic ulcer and tumor bleeding: FOBT positive diagnosis rate for peptic ulcer is 40%~70%, showing intermittent positive; after treatment, when the appearance of stool is normal, FOBT can still be positive for 5~7 days , If the bleeding stops completely, the occult blood test can be converted to negative. The positive rate of digestive tract malignant tumors is 20% in the early stage and 95% in the late stage, and the positive rate is persistent

34. The main purpose of semen examination

u Evaluate male reproductive function, provide basis for infertility diagnosis and curative effect observation

u Auxiliary diagnosis of male reproductive system diseases

u Observation of curative effect after vasectomy

u Screen high-quality sperm for in vitro fertilization and sperm bank

u Forensic identification

35. Clinical significance of decreased sperm motility

Decreased sperm motility is an important factor in male infertility. When the sperm motility rate is lower than 70%, it can reduce fertility, and if it is lower than 40%, it can lead to infertility. There are many factors that cause the decline of sperm motility:

u Varicocele

u Reproductive system infection, such as gonorrhea, syphilis, etc.

u Physical factors: such as high temperature environment (hot water bath), radiation factors, etc.

u Chemical factors such as certain drugs (anti-metabolites, antimalarials, estrogens), ethanol, etc.

36. Common diseases of reduced sperm count

When the sperm count is continuously <20×109/L, it is oligospermia; when there is no sperm in the semen multiple times, it is azoospermia (3 consecutive inspections, and there is still no sperm in the sediment after centrifugation). Common in:

u After male ligation: Generally, the inspection starts at the 6th week after ligation, 1-2 times a week, and no sperm is detected for 3 consecutive times, which indicates that the operation is successful

u Testicular lesions: such as varicocele, testicular deformity, inflammation, tuberculosis, gonorrhea, tumor and cryptorchidism, etc.

u Vas deferens diseases: such as vas deferens obstruction, congenital defects of vas deferens and immune infertility

u Others: retrograde ejaculation, harmful metal or radiation damage, environmental factors, the elderly, application of anticancer drugs, etc.

37. Common formed components of prostatic fluid and their clinical significance

component

clinical significance

Phosphatidylcholine bodies

In prostatitis, phosphatidylcholine bodies can be reduced, piled up, or unevenly distributed; in severe inflammation, phosphatidylcholine bodies are phagocytized by phagocytic cells and disappear

prostate granulosa cells

Increase is more common in the elderly, prostatitis (can increase by 10 times, with a large number of pus cells)

amyloid body

Generally without clinical significance, it can combine with cholesterol to form prostate stones

red blood cells

Increases are seen in prostatitis, prostate stones, prostate tuberculosis or malignant tumors, and after prostate massage

leukocyte

Increased and clustered, one of the characteristics of chronic prostatitis

Trichomonas

The discovery of trichomonas can be diagnosed as trichomonas prostatitis

Pathogen

Corresponding infection

38. Trichomonas vaginalis and its detection principle

u Trichomonas vaginalis: belongs to flagellate class, is a kind of pathogenic anaerobic parasitic protozoa that parasitizes in the vagina. Insect body diameter 8~45

, in the shape of an inverted pear with a wide neck and tail tip, 2 to 3 times the size of white blood cells. There are 4 flagella at the top of the worm body and 1 flagella at the rear end. The optimum pH for its growth is 5.5-6.0, and the optimum temperature is 25-42°C. Can be transmitted through sexual contact or contaminated items, causing trichomonas vaginitis

u Detection principle: 1. Direct smear method: use normal saline hanging drop method to observe under high power microscope

2. After Wright or Glan staining, observe the insect body structure with an oil lens, which can improve the detection rate

3. Culture method and immunological method: such as latex agglutination test, monoclonal antibody inspection, enzyme-linked immunosorbent assay and polyclonal antibody latex agglutination method, etc.

39. Clinical significance of purulent leucorrhea and bloody leucorrhea

Variety

clinical significance

purulent

1. Yellow or yellow-green, smelly: trichomonal or purulent infection

2. Foamy purulence: trichomonas vaginitis

3. Others: chronic cervicitis, senile vaginitis, infantile vaginitis, amoebic vaginitis, endometritis, infection caused by pyometra and vaginal foreign bodies

Bloody

1. Bleeding: cervical polyps, uterine submucosal fibroids, senile vaginitis, severe chronic vaginitis, side effects of intrauterine devices, etc.

2. Bloody, with a special smell: malignant tumors (cervical cancer, uterine body cancer)

40. Formation of cerebrospinal fluid

u It is mainly actively secreted by the choroid plexus of the ventricle, and some cerebrospinal fluid can also be secreted by ependymal cells, and a small amount of cerebrospinal fluid is formed by vascular filtrate entering the subarachnoid space

41. Detection principle of total cell count in cerebrospinal fluid

u Instrument counting method: the body fluid cell analyzer can automatically analyze and count cells

u Microscopic counting method: 1. Relatively clear or slightly cloudy cerebrospinal fluid: Use a dropper to draw a little of the mixed cerebrospinal fluid sample, fill it into the blood cell counting board, let it stand for 2~3min, and count the four corners of the 2 counting chambers under a low-magnification microscope The number of cells in 10 large squares with the central large square, that is, the total number of cells per microliter of cerebrospinal fluid, and then converted into the total number of cells per liter of cerebrospinal fluid when reporting. 2. Too many cells, turbid or bloody cerebrospinal fluid: can be used The red blood cell diluent is diluted and then counted, and finally converted into the total number of cells per liter of cerebrospinal fluid

42. Application of cerebrospinal fluid examination in viral meningitis

u The cerebrospinal fluid is dominated by lymphocytosis, and neutropenia may also appear in the early stage, which is replaced by small and medium lymphocytes and activated lymphocytes with darker cytoplasmic staining within a few days. When the abnormal cells subside and the normal ratio of lymphocytes and monocytes reaches a normal ratio, it indicates that the condition has improved, otherwise it reflects the aggravation or recurrence of the condition. The protein is slightly increased, and the glucose and chloride are generally normal; those with increased AST activity in the cerebrospinal fluid have severe brain tissue damage and poor prognosis; specific IgM antibody detection can be used for early diagnosis

43. Clinical significance of increased protein content in cerebrospinal fluid

lesion

clinical significance

Inflammatory lesions of brain tissue

When the brain tissue is infected, the permeability of the capillaries of the meninges and choroid plexus increases, and albumin increases first, followed by globulin and fibrin

Radiculopathy

Such as obstructive hydrocephalus, Guillain-Barre syndrome, often protein-cell dissociation

spinal canal obstruction

The brain and the subarachnoid space are not connected to each other, the plasma protein leaks from the spinal vein, and the protein content in the cerebrospinal fluid increases significantly (sometimes up to 30-50g/L), such as spinal cord tumors, metastatic cancer, and adhesive arachnoiditis

other

The protein content in the cerebrospinal fluid of premature infants can reach 2g/L, and that of newborns is 0.8~1.0g/L, and it will gradually drop to normal levels after 2 months of birth.

44. Changes and clinical significance of cerebrospinal fluid glucose

Variety

clinical significance

reduce

1. For acute suppurative meningitis, tuberculous meningitis, and fungal meningitis, the lower the glucose content, the worse the prognosis

2. Brain tumors, especially malignant tumors

3. Neurosyphilis

4. Low blood sugar

increased

1. After a full meal or intravenous glucose injection, blood glucose levels increase

2. Cerebral hemorrhage

3. Acute trauma or poisoning affecting the brainstem

4. Diabetes

45. The clinical significance of elevated cerebrospinal fluid immunoglobulin

Immunoglobulin

clinical significance

IgG

Neurosyphilis, suppurative meningitis, tuberculous meningitis, viral meningitis, chorea, nervous system tumors, and multiple sclerosis

IgA

Purulent meningitis, tuberculous meningitis, viral meningitis, tumor, etc.

IgM

Purulent meningitis, viral meningitis, tumor, multiple sclerosis, etc.

IgE

brain parasites etc.

46. ​​Clinical significance of determination of chloride in cerebrospinal fluid

u Reduced: 1. Bacterial meningitis and fungal meningitis early, tuberculous meningitis

2. Vomiting, adrenal insufficiency and kidney disease

3. When viral encephalitis, poliomyelitis, or brain tumors occur, the cerebrospinal fluid chloride burn decreases or does not decrease

u increased: uremia, dehydration, heart failure and serous meningitis, etc.

47. Formation of serous cavity effusion

type

The mechanism

transudate

Increased capillary hydrostatic pressure

Reduced plasma colloid osmotic pressure

Blocked lymphatic drainage

sodium and water retention

exudate

Microbial toxins, hypoxia, and inflammatory mediators

Increased vasoactive substances, cancer cell infiltration

trauma, chemical irritation

48. Collection, preservation and reception of serous cavity effusion specimens

u Specimen collection:

Serosal cavity effusion specimens were collected by clinicians through serosal cavity puncture, and the middle fluid was collected in sterile test tubes, and appropriate anticoagulants were used for anticoagulation as needed. In addition, collect 1 tube of specimen without anticoagulant to observe whether the effusion has coagulation phenomenon

u Save and receive:

1. Proper storage: Specimens should be checked in time after receipt. The routine and chemical examination of serous cavity effusion must be completed within 2 hours after collection, otherwise the specimen should be refrigerated. Specimens can be stored for 24 hours if cytology counts and differentials are performed

2. Pay attention to the logo (zhì): the logo of the specimen collection container should be consistent with the inspection application form

49. Clinical significance of lactate dehydrogenase (LD) and adenosine deaminase (ADA) examination in serous cavity effusion

LD:

The detection of effusion LD is mainly used to identify the nature of effusion. Exudate LD has the highest activity in purulent infection effusion, and its average value can reach 30 times that of normal serum, followed by malignant effusion, and tuberculous effusion is slightly higher than that of normal serum. serum. The LD of malignant pleural effusion is about 3.5 times that of autologous serum, while that of benign pleural effusion is about 2.5 times

ADA:

The detection of ADA in serosal effusion is mainly used to differentiate tuberculous and malignant effusion. The ADA of tuberculous effusion is significantly increased, and >40U/L should be considered as tuberculous. The specificity for the diagnosis of tuberculous pleural effusion reaches 99%. , Superior to methods such as tuberculin test, bacteriology and biopsy. ADA decreases when anti-tuberculosis drug treatment is effective, so it can be used as an observation index for the effect of anti-tuberculosis treatment

50. Laboratory identification of exudate and transudate

project

transudate

exudate

Etiology

non-inflammatory

Inflammatory trauma, tumor or physical and chemical stimulation

color

pale yellow

yellow, red, milky white

transparency

clear transparent or amber

cloudy or chylus

proportion

<1.015

>1.018

pH

>7.3

<7.3

Coagulation

Not easy to solidify

Easy to solidify

Rivalta test

Negative

Positive

Protein content (g/L)

<25

>30

effusion protein/serum protein

<0.5

>0.5

Glucose (mmol/L)

close to blood sugar level

<3.33

LD(U/L)

<200

>200

Effusion LD/serum LD

<0.6

>0.6

Total number of cells (×106/L)

<100

>500

nucleated cell sorting

Predominantly lymphocytes, mesothelial cells may be seen

Acute inflammation is dominated by neutrophils, chronic inflammation or malignant effusion is dominated by lymphocytes

tumor cells

none

may have

bacteria

none

may have

Review points of exfoliative cytology

1. What is the epithelial type of the endometrium? Squamous epithelium, secretory glandular epithelium, ciliated epithelium , mesothelial cells

2. What is the cytoplasmic color of the parakeratized squamous epithelium in the Pap stainer?

3. What are the characteristics of nuclear chromatin in prekeratinized cells? Meticulous and even

4. What kind of cells are generally used as the ruler for comparison with other cells in the smear? red blood cells

5. What structure is the well-differentiated adenocarcinoma arranged in? entity structure

6. What structures are poorly differentiated adenocarcinomas arranged in?

7. What are the main manifestations of virus-infected cells? multi-core

8. What are the advantages of Papanicolaou staining? Cell transparency is good, the structure is clear, and the smear is rich and bright in color. Because it can show the different degrees of keratinization of the squamous epithelium, it is often used in vaginal smears to determine estrogen levels. Poorly differentiated squamous cell carcinoma small keratinocytes in cervical smears and sputum smears are orange-yellow, especially prominent in the red necrotic background, so it is difficult to miss the diagnosis

This staining method not only has the characteristics of clear nuclear structure, clear color separation, good transparency, and bright cytoplasm, but also the stained specimen is not easy to decolorize and can be stored for a long time.

9. Which type of cancer are signet ring cancer cells usually seen in? well differentiated adenocarcinoma

10. Which kind of cancer are pleomorphic cancer cells usually found in? Well differentiated squamous cell carcinoma

11. Well differentiated squamous cell carcinoma is equivalent to which layer of cancer cells?

12. Malignant cells derived from epithelial cells are called? cancer cell

13. Briefly describe cancer cell clusters and their characteristics: In cancer cell clusters, the cells are of different sizes, arranged in disorder, losing polarity, squeezing each other, mosaic or stacked.

14. Which tumor is more sensitive to radiotherapy? Retinoblastoma, nasopharyngeal carcinoma, dysgerminoma in ovarian cancer, testicular seminoma, renal embryonal tumor, malignant lymphoma, etc.

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