Etiology Consideration for Presenting Complaints – Part: 1

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Hematology & Oncology

Anemia with low MCV

  • Iron deficiency- blood loss, pregnancy, dietary deficiency, PUD, HHT
  • Malignancy- gastric and colonic carcinoma
  • GIT- IBD, diverticulitis
  • Malabsorption- celiac disease, IBD
  • Thalassaemia- alpha & beta thalassaemia
  • Sideroblastic anemia
  • Anemia of chronic disease
  • Bleeding & hemolysis ( high reticulocyte count)

Anemia with high MCV

  • Folate deficiency- dietary deficiency, malabsorption, celiac, surgery, pregnancy, hemolysis, OCP, phenytoin MTX
  • B12 deficiency- dietary, gastrectomy, pernicious, SIBO, Crohn’s, fish tapeworm
  • Alcohol
  • Hypothyroid
  • Myelodysplasia
  • Hypercholesterolemia
  • Bleeding and hemolysis

Lymphadenopathy

  • Infective- bacterial, viral, protozoal, fungal
  • Neoplastic- primary- lymphoma, leukemia; secondary- lung, breast, thyroid, stomach, melanoma
  • CTD- RA, SLE
  • Sarcoidosis, amyloidosis, AOSD, Phenytoin

Splenomegaly

  • Hematological- megaloblastic anemia, hemoglobinopathies (thalassemia), hereditary spherocytosis; AIHA; MPD- CML, MF, PRV, ET; Leukaemia, lymphoma
  • Congestive- Liver- CLD with portal HTN, portal vein thrombosis, hepatic vein occlusion; cardiac-chronic CCF, constrictive pericarditis
  • Infective- TB, salmonella, brucella, infective endocarditis, viral- hepatitis, CMV, EBV; malaria, kala-azar, histoplasmosis, trypanosomiasis, melioidosis
  • Inflammatory- felty’s in RA, sarcoidosis, SLE
  • Others- metastatic cancer, lysosomal storage disease- Gaucher’s, Niemann-pick; splenic cyst, amyloid, thyrotoxicosis

Thrombocytopenia

  • Decreased production

Marrow hypoplasia- congenital- fanconi’s anemia, aplastic anemia, drugs- cytotoxics,
antimetabolites, transfusion-associated GVHD
Marrow infiltration- leukaemia, myeloma, carcinoma, myelofibrosis, storage disease
B12 or folate deficiency
Familial thrombocytopathies – abnormal platelets, Bernard-soulier, wiskott-aldrich syndrome

  • Increased consumption
  1. Immune- ITP(CTD, SLE, HIV, B cell malignancy, pregnancy, drugs) , post transfusion, drugs-quinine, vancomycin, heparin
  2. Coagulation activation- DIC
  3. Mechanical pooling- hypersplenism
  4. Thrombotic microangiopathies- HUS, TTP, liver disease, pre-eclampsia
  5. Others- gestationa, type2b VWD

Venous thrombosis

  • Patient factors- age, immobility, obesity, varicose vein, previous DVT, positive family history, pregnancy, puerperium, OCP, long-distance travel >4hrs, IVDU
  • Surgical conditions- major surgery, abdominal or pelvic surgery, lower limb orthopedic surgery
  • Medical conditions- ( head to toe) – stroke, GBS, paraplegia, MI, heart failure, pneumonia, COPD, IBD, nephrotic syndrome, malignancy in tummy or pelvis
  • Hematological conditions- PNH, PRV, essential thrombocythaemia, protein C protein S deficiency, factor V leiden mutation, myelofibrosis
  • APS

Oncological consideration in etiology

  • Weight loss- occult malignancy ( GIT, Lung)
  • Back pain- metastasis to vertebra from primary ( PUBLIK-T) ( prostate, urinary bladder, bronchus, breast, liver, intestine, kidney, thyroid)? multiple myeloma
  • Dyspnea- superior vena cava obstruction due to malignancy? lymphoma, SCLC
  • Spinal cord compression- paraplegia with urine retention
  • Hypercalcemia- metastasis, multiple myeloma
  • Fever- neutropenic fever
  • Acute renal impairment- tumor lysis syndrome

Aplastic anemia

  1. Primary idiopathic aplastic anemia
  2. Secondary-
    • Viral hepatitis
    • Pregnancy
    • Radiation therapy
    • Paroxysmal nocturnal hemoglobinuria
    • Chemicals- benzene, toluene solvent, insecticides, DDT, OPC, carbamates
    • Drugs- cytotoxic drugs, antibiotics- chloramphenicol, sulphonamides, indomethacin, gold, penicillamine, phenylbutazone, carbimazole, propylthiouracil, anticonvulsants, phenytoin
    • Fanconi’s syndrome
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