Egyptian Board Clinical Pathology flashcards
Egyptian Board Clinical Pathology · Build recall with a focused review session.
31 cards. Read the term and the definition here. The deck at the top of this page is optional.
- Anion gap formula
- Anion gap equals sodium minus the sum of chloride and bicarbonate, normally 8–12 mmol/L. A raised gap indicates accumulation of unmeasured anions such as lactate, ketones, or toxins.
- Corrected calcium formula
- Corrected calcium in mmol/L equals measured calcium plus 0.02 times (40 minus albumin in g/L). This adjusts for albumin-bound calcium but does not replace measurement of ionised calcium.
- Friedewald LDL limitation
- The Friedewald equation estimates LDL as total cholesterol minus HDL minus triglycerides divided by 2.2 in mmol/L. It is invalid when triglycerides exceed about 4.5 mmol/L, so direct LDL or non-HDL cholesterol is used.
- Osmolal gap
- The osmolal gap is measured osmolality minus calculated osmolality (2Na plus glucose plus urea). A gap above 10 mOsm/kg suggests unmeasured osmoles such as methanol or ethylene glycol.
- HbA1c interpretation limits
- HbA1c reflects mean glucose over the preceding 8–12 weeks. Results are unreliable in haemoglobinopathies, recent transfusion, pregnancy, and chronic kidney disease, where alternative glycaemic markers are needed.
- Troponin kinetics
- Cardiac troponin rises 3–6 hours after myocardial injury and peaks at 12–24 hours. A single value cannot exclude acute coronary syndrome, so serial sampling with a 0/1-h or 0/3-h algorithm is required.
- Iron deficiency versus chronic disease
- Iron deficiency shows low ferritin and transferrin saturation below 20%. Anaemia of chronic disease shows low serum iron, low TIBC, and normal or high ferritin due to hepcidin-mediated iron sequestration.
- ABO compatibility rules
- Group O red cells are the universal red cell donor; group AB plasma is the universal plasma donor. Group O plasma contains anti-A and anti-B and must not be given to non-O recipients.
- Acute haemolytic transfusion reaction
- Presents with fever, chills, flank pain, haemoglobinuria, and DIC. Management is to stop the transfusion immediately, maintain venous access, support blood pressure, and send samples for DAT and repeat crossmatch.
- DIC laboratory profile
- Disseminated intravascular coagulation shows prolonged PT and APTT, low fibrinogen, raised D-dimer, thrombocytopenia, and schistocytes on the blood film. Treatment targets the underlying cause.
- Blood component storage
- Red cells are stored at 2–6 °C for up to 35–42 days. Platelets are agitated at 20–24 °C for 5–7 days. Fresh frozen plasma is frozen within 8 hours and used within 24 hours after thawing.
- Warfarin versus heparin monitoring
- Warfarin is monitored by INR because it reduces functional factors II, VII, IX, and X. Unfractionated heparin is monitored by APTT and low molecular weight heparin by anti-Xa activity.
- Hepatitis B serology patterns
- HBsAg indicates current infection. Anti-HBc IgM indicates acute infection. Anti-HBs indicates immunity after vaccination or resolved infection. Anti-HBc IgG with anti-HBs indicates past infection.
- HIV diagnostic algorithm
- A fourth-generation combined antigen/antibody assay is the screen. Reactive results are confirmed by Western blot or HIV-1/2 differentiation immunoassay, with HIV RNA PCR used for indeterminate or acute cases.
- Syphilis serology interpretation
- Non-treponemal tests (VDRL, RPR) quantify disease activity and monitor treatment. Treponemal tests (TPHA, EIA) remain positive for life and are used to confirm the diagnosis.
- Dengue serology timing
- NS1 antigen is detectable in the first 5 days of illness. IgM appears from about day 5. Rapidly rising IgG suggests secondary infection.
- Gram stain principle
- Gram-positive organisms retain the crystal violet–iodine complex because of thick peptidoglycan. Gram-negative organisms decolourise and take up the safranin counterstain, appearing pink.
- ANA testing strategy
- Antinuclear antibody immunofluorescence is a screening test. Positive results require confirmation with anti-dsDNA, which tracks SLE activity, and anti-extractable nuclear antigen antibodies for specific connective tissue diseases.
- Complement pattern interpretation
- Low C3 and C4 with normal total haemolytic complement suggests classical pathway consumption, as in SLE or cryoglobulinaemia. Low C3 with normal C4 suggests alternative pathway activation.
- Hypersensitivity types
- Type I is IgE-mediated mast cell degranulation. Type II is antibody-mediated cytotoxicity. Type III is immune complex deposition. Type IV is delayed T-cell-mediated hypersensitivity.
- Anti-CCP versus rheumatoid factor
- Anti-CCP has higher specificity than rheumatoid factor for rheumatoid arthritis. Rheumatoid factor is also positive in Sjögren syndrome, hepatitis C, and some healthy elderly individuals.
- Coeliac serology
- Tissue transglutaminase IgA is the preferred screen, interpreted with a total IgA level. IgA deficiency causes false negatives and requires IgG-based assays such as IgG anti-tTG or anti-endomysial antibodies.
- Formalin fixation parameters
- Ten percent neutral buffered formalin penetrates at roughly 1 mm per hour. Recommended fixation is 6–48 hours for small biopsies and longer for large specimens, to preserve morphology and antigenicity.
- Frozen section indications
- Frozen section is used for intraoperative diagnosis, margin assessment, and confirmation of lesional tissue. It is unsuitable for lymphoid or subtle lesions because freeze artefact distorts nuclear detail.
- Bethesda cytology systems
- The Bethesda system standardises cervical cytology (NILM, ASC-US, LSIL, HSIL, AGC, cancer) and thyroid cytology (categories I–VI). Standardised categories guide management and allow comparison between laboratories.
- Immunohistochemistry lineage markers
- Cytokeratin confirms epithelial lineage, vimentin mesenchymal lineage, S100 neural crest origin, and CD45 leucocyte lineage. Interpretation requires external and internal controls to exclude non-specific staining.
- PCR contamination control
- Separate pre- and post-amplification areas, use uracil-N-glycosylase, and include negative extraction and no-template controls. These measures prevent and detect amplicon contamination that causes false-positive results.
- ACMG variant classification
- Variants are classified as pathogenic, likely pathogenic, variant of uncertain significance, likely benign, or benign. Classification integrates population frequency, computational prediction, functional data, and segregation evidence.
- Karyotype versus FISH
- Karyotyping requires cultured dividing cells and detects balanced translocations and numerical changes. FISH detects targeted deletions, duplications, and translocations on interphase cells without culture.
- Westgard multirules
- The 12s rule is a warning. The 13s, 22s, R4s, 41s, and 10x rules are rejection rules indicating random or systematic error in internal quality control.
- Six Sigma in the laboratory
- Sigma equals total allowable error minus bias, divided by coefficient of variation. Values above 6 indicate excellent performance, while values below 3 indicate unacceptable performance requiring process improvement.