Internal Diseases – Part 1 (Rheumatology, Pulmonology, Phthisiatrics, Cardiology, Haematology) · MU Plovdiv

6. Aplastic anemia

Inside: 10 sections · 1 table · 16 flashcards · 5 min

Topic 55 of 68 in the MU Plovdiv syllabus for Internal Diseases – Part 1 (Rheumatology, Pulmonology, Phthisiatrics, Cardiology, Haematology) (Medicine, Year 4). The free AceMed note covers it in 9 sections, about 934 words (5 min of reading), with 16 flashcards.

In this note

  1. Essay 6- Aplastic anemia
  2. Definition
  3. Etiology
  4. Classification
  5. Pathogenesis
  6. Symptoms
  7. Diagnosis
  8. Treatment
  9. Aplastic anemia. Agranulocytosis

Definition

  • Aplastic anemia is a pancytopenia resulting from hypoplasia of the bone marrow!

Etiology

Table 22.2 Causes of aplastic anaemia.

EBV, Epstein–Barr virus.

Classification

  • Primary- develops without evidence of underlying disease
  • Secondary- develops due to another pathological process occurring in the body

Pathogenesis

  • The underlying defect in all cases appears to be a substantial reduction in the number of haemopoietic pluripotential stem cells, and a fault in the remaining stem cells or an immune reaction against them

Symptoms

  • Onset is at any age, with peak incidence around 10-25 and over 60 year olds
  • Sudden onset febrile illness
  • Bruising
  • Bleeding gums
  • Epistaxis
  • Menorrhagia
  • Retinal hemorrhage may impair vision
  • Frequent infections of mouth and throat

Diagnosis

  • CBC- there must be at least 2 of the following:
  • Anemia (normochromic, normocytic or macrocytic)
  • Reticulocyte count is very low in relation to the degree of anemia
  • Neutropenia
  • Thrombocytopenia
  • No abnormal cells in peripheral blood
  • Bone marrow shows hypoplasia with loss of hematopoetic tissue and replacement by fat
  • Bone marrow biopsy:
  • Hypocellular and devoid of marrow progenitors

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