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Severe homozygous HbE disease: the first case report from Nepal.

Urza BhattaraiDibasha AdhikariArun GautamAyush AnandBhupendra ShahSanjib Kumar Sharma
Published in: Oxford medical case reports (2023)
Hemoglobin E (HbE) is the most prevalent hemoglobinopathy in the eastern Indian subcontinent. We presented the case of a 53-year-old male from Nepal with a history of multiple blood transfusions who presented with abdominal fullness for 15 years and easy fatigability for 2 months. He had pallor and massive splenomegaly. Laboratory parameters showed pancytopenia with microcytic anemia, indirect hyperbilirubinemia, target cells in the peripheral smear and iron overload. A computed tomography scan of the abdomen showed multiple splenic infarcts. Hemoglobin electrophoresis was suggestive of HbE homozygous disease. Based on these findings, we made a diagnosis of HbE homozygous disease. We provided symptomatic treatment and folic acid supplementation and counseled him for splenectomy and genetic screening. Our case highlighted the uncommon presentation of Hb E disease.
Keyphrases
  • computed tomography
  • magnetic resonance imaging
  • induced apoptosis
  • chronic kidney disease
  • positron emission tomography
  • gene expression
  • signaling pathway
  • mycobacterium tuberculosis
  • pulmonary tuberculosis