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GERICLINICS

GeriQBank · Topic

Haematology, Oncology & Screening

Anaemia, haematological disorders, cancer and cancer screening.

Questions
50
High-yield
7
Set twice or more
Times set
27
Papers III–IV, 2009–2025
Completed in Haematology, Oncology & Screening—

Very High Yield(6)

Set 3 or more times

  1. Paper III15-mark essay + 7-mark note

    WHO Classification & Diagnostic Criteria of MDS, and its Differentials

    Exceptionally well covered: Pathy's Ch. 26/27, Tables 26.1–26.4 and 27.1 — directly quotable. Subtype Dysplastic lineages Ring sideroblasts Blasts MDS-SLD 1 <15% (<5% if SF3B1+) PB<1%, BM<5% MDS-RS 1–3 ≥15% (≥5% if SF3B1+) PB<1%, BM<5%…

    Very High YieldAsked ×5
  2. Paper III15-mark essay + 7-mark note

    Myelodysplastic Syndrome

    Myelodysplastic Syndrome Describe the WHO classification and diagnostic criteria of myelodysplastic syndrome. Discuss its differential diagnosis. (15 marks) Definition. Myelodysplastic syndromes are clonal disorders of the…

    Very High YieldAsked ×5
  3. Paper IV7-mark note + 15-mark essay

    Cancer screening in the elderly — currently accepted strategies

    Primary source: Pathy's, 6th ed. — "Preventive Geriatrics"; Essentials of Clinical Geriatrics, 7th ed. — "Prevention". Screening is secondary prevention — detection of disease in the preclinical phase. Essentials states that the value…

    Very High YieldAsked ×4
  4. Paper IV7-mark note

    Screening for colorectal cancer

    Primary source: Pathy's, 6th ed.; Essentials of Clinical Geriatrics, 7th ed. The prevalence of carcinogenesis increases along the entire gastrointestinal tract with age, driven by mucosal irritation, inflammation, impaired antioxidant…

    Very High YieldAsked ×4
  5. Paper IV7-mark note + 6-mark note

    Mammography — screening the older woman

    Primary source: Pathy's, 6th ed. — "Preventive Geriatrics"; Essentials of Clinical Geriatrics, 7th ed. — "Prevention". Mammography is the mainstay of breast cancer screening. Research has shown mammography to be effective up to age 84 —…

    Very High YieldAsked ×4
  6. Paper III15-mark essay + 7-mark note

    Myelodysplasia

    Well covered: Pathy's Ch. 26 ("Myelodysplasia") and Ch. 27 ("Management of MDS and AML in the Elderly") cover this topic in genuine depth — this answer is largely textbook-derived. Heterogeneous clonal haematopoietic stem cell disorders…

    Very High YieldAsked ×3

High Yield(1)

Set twice

Moderate Yield(18)

Set once

  1. Paper II7-mark note

    Paraneoplastic syndromes

    Definition. Remote, non-metastatic effects of malignancy mediated by tumour-secreted hormones, cytokines or cross-reacting onconeural antibodies — not by tumour mass, local invasion or metastasis. They are important because they are…

    Moderate YieldAsked ×1set in Paper III
  2. Paper II7-mark note

    Tumour lysis syndrome

    Definition and mechanism. An oncological emergency caused by massive lysis of tumour cells, spontaneously or after cytotoxic therapy, releasing intracellular contents into the circulation faster than the kidney can clear them. This…

    Moderate YieldAsked ×1set in Paper III
  3. Paper III7-mark note

    Anaemia of Chronic Disease

    Well covered: Pathy's Ch. 22, under "Inflammatory Anaemias", with Figures 22.3 and 22.5. Anaemia from inflammation with excess cytokine production — a functional iron deficiency (stores normal/high, but unavailable for erythropoiesis).…

    Moderate YieldAsked ×1
  4. Paper III7-mark note

    Thrombocytopenia

    Well covered: Pathy's Ch. 24 ("Disorders of Platelet Number"), supplemented by Ch. 23 (DIC). Definition: platelet count <1,50,000/µL. Platelet count does NOT change with normal ageing — a low count always signifies disease. Haemostasis…

    Moderate YieldAsked ×1
  5. Paper III7-mark note

    Hodgkin Lymphoma

    Textbook gap: No Hodgkin lymphoma chapter. Only link: Ch. 26 — actuarial risk of therapy-related MDS/AML is 6–9% after Hodgkin's treatment (vs 17% after myeloma treatment). Geriatric-oncology philosophy from Ch. 26/27 transfers…

    Moderate YieldAsked ×1
  6. Paper III7-mark note

    Anaemia of Chronic Kidney Disease — Type, Investigation & Treatment

    Well covered: Pathy's Ch. 22, dedicated CKD section with Figure 22.3. Normocytic, normochromic, HYPOPROLIFERATIVE anaemia — reticulocytes low for the degree of anaemia. 45–70% of adults over 75 meet CKD criteria (GFR<90); 51–60% of CKD…

    Moderate YieldAsked ×1
  7. Paper III7-mark note

    Mechanisms of Drug-Induced Thrombocytopenia

    Covered briefly: Pathy's Ch. 24 gives the two-mechanism framework and HIT in detail; the six-antibody subdivision below is externally sourced. Pathy's rule: "Prescription drugs should ALWAYS be considered as a possible cause in any case…

    Moderate YieldAsked ×1
  8. Paper III7-mark note

    Blood Transfusion

    Partial coverage: No dedicated transfusion chapter, but elderly-specific PRACTICE is discussed substantially across Ch. 22 (CKD), Ch. 23 (DIC), Ch. 24 (platelet thresholds) and Ch. 26/27 (MDS transfusion support — the most detailed…

    Moderate YieldAsked ×1
  9. Paper III7-mark note

    Bone Marrow Transplant

    No standalone chapter, but Ch. 27 discusses allogeneic HSCT in real depth, framed around age eligibility — directly quotable. Definition: conditioning regimen + infusion of HLA-compatible stem cells. Allogeneic (curative, immune…

    Moderate YieldAsked ×1set in Paper IV
  10. Paper III7-mark note

    POEMS Syndrome

    Complete textbook gap. Only tangential link: the standard peripheral neuropathy work-up algorithm (Essentials of Clinical Geriatrics, Fig. 13-3) includes SPEP/UPEP/IPEP for any acquired demyelinating neuropathy — the pathway that would…

    Moderate YieldAsked ×1set in Paper IV
  11. Paper III7-mark note

    Bone Marrow Transplantation

    Bone Marrow Transplantation Discuss the types, indications, procedure and complications of bone marrow transplantation, with emphasis on the older patient. Definition. Bone marrow transplantation — more accurately haematopoietic stem…

    Moderate YieldAsked ×1set in Paper IV
  12. Paper III7-mark note

    POEMS Syndrome

    POEMS Syndrome Describe the clinical features, laboratory investigations and treatment of POEMS syndrome. (15 marks) Definition. POEMS syndrome is a rare multisystem paraneoplastic disorder caused by an underlying clonal plasma cell…

    Moderate YieldAsked ×1set in Paper IV
  13. Paper III6-mark note

    Hormone Therapy in Malignancy

    Hormone Therapy in Malignancy Discuss the principles, agents, indications and adverse effects of hormone therapy in malignancy, with emphasis on the older patient. (15 marks) The governing statement. A number of cancers prevalent in the…

    Moderate YieldAsked ×1
  14. Paper IV7-mark note

    Tumour markers — role in detection and management of cancer

    Molecules that show the presence of cancer or give information about how it will behave, for example its likelihood of progressing or responding to treatment. An ideal marker would have high positive and negative predictive values; be…

    Moderate YieldAsked ×1
  15. Paper III7-mark note

    Approach to a suspicious breast lesion in an older woman

    Confirm the diagnosis fully, then match treatment to fitness, frailty and the woman's wishes rather than to her age. Age-related variation in treatment is common, and many older women receive primary endocrine therapy, which may worsen…

    Moderate YieldAsked ×1

Low Yield(5)

Not set in 2009–2025 papers

  1. Paper III

    Name the various plasma cell dyscrasias

    Textbook gap: Pathy's has no dedicated chapter on plasma cell dyscrasias. Only incidental mentions exist in Ch. 24 (paraproteins as a cause of acquired coagulation defects — myeloma, MGUS, amyloid; inhibition of fibrin polymerisation;…

    Low Yield
  2. Paper III

    Multiple Myeloma — Aetiology, Diagnosis & Management

    Textbook gap: No myeloma chapter in Pathy's. Transferable content: Ch. 24 (paraprotein coagulopathy), Anaemia chapter (clonal anaemia), Ch. 59 (spinal red flags), and — most valuably — Ch. 26/27's geriatric-oncology philosophy (CGA is…

    Low Yield
  3. Paper III

    Chronic Myeloid Leukaemia — Clinical Features & Management

    Textbook gap: Pathy's mentions CML only once — Ch. 24, Table 24.2 — as a myeloproliferative disorder causing acquired platelet dysfunction (bleeding paradoxically more common when platelets >10,00,000/µL). Everything else is externally…

    Low Yield

Not rated(20)

No university frequency data yet

  1. Paper II7 marks

    Anaemia in the elderly and the evaluation of anaemia

    Definition and magnitude. Anaemia is defined by WHO as haemoglobin below 13 g/dL in men and below 12 g/dL in women. Prevalence rises steeply with age — about 10% over 65 years and over 20–25% beyond 85 years, and higher still in nursing…

    Not rated
  2. Paper II7 marks

    Iron deficiency anaemia — red cell indices and investigation

    Definition. Anaemia (WHO: Hb <13 g/dL in men, <12 g/dL in women) resulting from depleted body iron stores. It is the commonest anaemia worldwide and the commonest nutritional anaemia in Indian elderly. In an older adult, iron deficiency…

    Not rated
  3. Paper II15 marks

    Megaloblastic anaemia and B12 deficiency

    Definition. A macrocytic anaemia caused by impaired DNA synthesis from vitamin B (cobalamin) or folate 12 deficiency, producing nuclear-cytoplasmic asynchrony and ineffective erythropoiesis. Physiology of B absorption. Dietary B binds…

    Not rated
  4. Paper II7 marks

    Anaemia of chronic disease

    Definition. Also called anaemia of inflammation — a mild to moderate, usually normocytic normochromic anaemia occurring in chronic infection, inflammation or malignancy. It is the second commonest anaemia worldwide and the commonest…

    Not rated
  5. Paper II7 marks

    Blood transfusion in the older adult — thresholds and hazards

    Guiding principle. Transfuse for symptoms and physiology, not for a number. Give a single unit and then reassess ("why give two when one will do"), and always consider treating the cause — iron, B , folate or 12 erythropoietin — instead…

    Not rated
  6. Paper II7 marks

    Thrombocytopenia

    Definition and bleeding risk. Platelet count below 150 × 109/L. Spontaneous bleeding is unusual above 50, purpura and mucosal bleeding appear below 30, and the risk of spontaneous serious or intracranial bleeding rises below 10–20 ×…

    Not rated
  7. Paper II7 marks

    Disseminated intravascular coagulation

    Definition. An acquired syndrome of widespread intravascular activation of coagulation with loss of localisation, causing microvascular thrombosis with organ dysfunction and simultaneous consumption of platelets and clotting factors…

    Not rated
  8. Paper II7 marks

    Myelodysplasia

    Definition. Myelodysplastic syndromes are clonal haematopoietic stem cell disorders characterised by ineffective haematopoiesis — a hypercellular or normocellular marrow with peripheral cytopenias — morphological dysplasia, and a…

    Not rated
  9. Paper II7 marks

    Chronic myeloid leukaemia — clinical features and management

    Definition and cytogenetics. A myeloproliferative neoplasm defined by the Philadelphia chromosome — t(9;22) (q34;q11) — producing the BCR::ABL1 fusion gene, which encodes a constitutively active tyrosine kinase. Median age at diagnosis…

    Not rated
  10. Paper II15 marks

    Chronic lymphocytic leukaemia

    Definition. A monoclonal proliferation of mature B lymphocytes, defined by ≥5 × 109/L clonal B lymphocytes in peripheral blood persisting for at least 3 months with a characteristic immunophenotype. It is the commonest leukaemia of…

    Not rated
  11. Paper II15 marks

    Myelofibrosis and the myeloproliferative neoplasms

    Definition and classification. Myeloproliferative neoplasms are clonal haematopoietic stem cell disorders with effective but dysregulated proliferation of one or more myeloid lineages. Philadelphia-negative: polycythaemia vera (PV),…

    Not rated
  12. Paper II15 marks

    Multiple myeloma — aetiology, diagnosis and management

    Definition and epidemiology. A malignant clonal proliferation of bone marrow plasma cells producing a monoclonal immunoglobulin, with resultant lytic bone disease, marrow failure and renal impairment. It accounts for about 10% of…

    Not rated
  13. Paper II7 marks

    Bone marrow transplantation in older patients

    Types. Autologous transplantation uses the patient's own stem cells after high-dose chemotherapy (myeloma, relapsed lymphoma) — no graft-versus-host disease and lower transplant-related mortality. Allogeneic transplantation uses donor…

    Not rated
  14. Paper II7 marks

    Prostatic cancer

    Epidemiology and risk factors. The commonest non-cutaneous cancer in men; incidence rises steeply with age, with median age at diagnosis around 66–70 years and latent histological cancer present in over 70% of men above 80 at autopsy.…

    Not rated
  15. Paper II7 marks

    Indications and rationale for cancer screening in the elderly

    Principles of screening (Wilson and Jungner). Screening is justified when the condition is an important health problem with a recognisable latent or early symptomatic stage, the natural history is understood, there is an acceptable,…

    Not rated
  16. Paper II6 marks

    Positron emission tomography

    Principle. PET is a functional (metabolic) imaging technique using a positron-emitting radionuclide attached to a biologically active molecule. The emitted positron annihilates with an electron to release two 511 keV gamma photons at…

    Not rated
  17. Paper III

    Anaemia in the Elderly & Evaluation of Anaemia

    Well covered: Pathy's Ch. 22 (Figures 22.1, 22.3, 22.4) — largely textbook-derived. Definition: Hb <13 g/dL men, <12 g/dL women — but also track the trend from the patient's own baseline. Anaemia is NOT normal ageing — signifies…

    Not rated