Course Content
Zambian Paediatric & Obstetrics-Gynecology (OB/GYN) Clinical Mastery

Paediatric Aplastic Anaemia 

Lesson Objectives

By the end of this lesson, learners should be able to:

  1. Define aplastic anaemia and recognize laboratory diagnostic criteria.

  2. Identify clinical features and congenital vs. acquired forms.

  3. List differential diagnoses for bone marrow failure.

  4. Outline appropriate investigations for diagnosis and severity assessment.

  5. Describe supportive, infection prophylactic, and definitive treatments including HSCT and immunosuppressive therapy.

  6. Monitor response to therapy and adjust management accordingly.

Description

Aplastic anaemia is pancytopenia resulting from bone marrow failure, with hemoglobin <10 g/dL, platelet count <50 × 10⁹/L, and granulocytes <1.5 × 10⁹/L. Bone marrow aspirate and trephine show hypocellularity without significant fibrosis or malignant infiltration.

It may be acquired due to infections, drugs, toxins, or autoimmune conditions, or inherited as part of bone marrow failure syndromes such as Fanconi anaemia or Shwachman-Diamond syndrome.

Clinical Features

Feature Description
Pallor Secondary to anemia
Easy bruising / Spontaneous bleeding Epistaxis, petechiae, purpura
Lymphadenopathy / Hepatosplenomegaly May indicate underlying disorder or secondary infection
Joint swelling Occasionally seen in autoimmune or congenital syndromes
Jaundice Suggests hemolysis or liver involvement
Congenital features Café au lait spots, short stature, limb/nail/digit abnormalities

Differential Diagnosis

Acquired Inherited
Viral infections: Hepatitis A, B, C, CMV, HIV Fanconi anaemia, Dyskeratosis congenita, Shwachman-Diamond syndrome
Medications/toxins: Benzene, chloramphenicol, cytotoxic drugs, radiation Pancytopenia associated with primary immunodeficiency
Nutritional deficiencies: Zinc, copper, B12, folate Myelodysplastic syndrome, PNH
Rheumatologic disorders

Investigations

Investigation Purpose / Findings
FBC, differential, peripheral smear, reticulocyte count Confirm pancytopenia
Hb electrophoresis Rule out haemoglobinopathies
Bone marrow aspirate and trephine (BMAT) Assess cellularity, exclude fibrosis/malignancy
Liver function tests (ALT, AST, ALP, bilirubin, albumin, GGT, INR/PTT) Assess liver involvement
Electrolytes (Na, K, Cl, Ca, Mg, Phosphate) Baseline metabolic status
Renal function tests (urea, creatinine) Assess kidney function
DAT, haptoglobin, LDH, ESR Evaluate hemolysis and inflammation
Iron studies (serum iron, ferritin, transferrin) Assess iron status
Viral studies Hepatitis A, B, C, CMV, HIV
Autoimmune tests ANA, dsDNA, RF, complement (C3/C4, CH50), immunoglobulins
Vitamin assays B12, serum and red cell folate
HLA typing For potential stem cell transplant

Investigations for inherited forms: Chromosomal breakage (Fanconi anaemia), flow cytometry for CD55/CD59 (PNH), SBDS gene testing (Shwachman-Diamond), telomere length (Dyskeratosis congenita), abdominal ultrasound for congenital anomalies.

Supportive Management

Step Action
Blood transfusion PRBCs to maintain Hb >7 g/dL; platelets to maintain >10 × 10⁹/L (well) or >20 × 10⁹/L (febrile)
Fever / neutropenia Neupogen (G-CSF) 5 mcg/kg/day SC; escalate up to 60 mcg/kg/day or 1,500 mcg/day if severe/refractory
Infection prevention PJP prophylaxis: pentamidine (300 mg inhaled q4w >6 yrs; IV <6 yrs), dapsone (avoid in G6PD deficiency)
Fungal prophylaxis Fluconazole 3 mg/kg/day IV/PO (max 400 mg/day); monitor interactions with cyclosporine

Definitive Treatment

Scenario Treatment
Matched sibling donor available Hematopoietic stem cell transplant (HSCT), ~90% cure rate; HLA typing required; arrange via UTH Children’s Hospital
No matched sibling donor Immunosuppressive therapy (IST) with admission: baseline labs, FBC, liver/renal function, electrolytes
IST regimen ATG 40 mg/kg IV daily ×4 days; prednisolone 1 mg/kg PO BID ×7 days, taper over 3 weeks; cyclosporine 5 mg/kg PO q12h, adjust to maintain trough 150–200 mcg/L
Pre-medications for IST Paracetamol 15 mg/kg PO pre-ATG q6h PRN; diphenhydramine 1 mg/kg PO/IV pre-ATG q6h PRN; pethidine 1 mg/kg IM q6h PRN

Post-IST: If no response at 3–6 months, consider unrelated donor HSCT with detailed family discussion.

Summary

  • Aplastic anaemia is pancytopenia from bone marrow failure.

  • Clinical signs: pallor, bleeding, bruising, jaundice, congenital anomalies.

  • Investigations: FBC, bone marrow, viral studies, autoimmune tests, iron and vitamin levels, HLA typing.

  • Supportive management: transfusion, infection prevention, G-CSF for neutropenia.

  • Definitive therapy: HSCT if sibling donor; IST if no donor.

  • Post-IST: monitor response, plan for unrelated donor transplant if necessary.

 

 

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