Hereditary Spherocytosis: Unravelling the Diagnostic Challenges

Cureus. 2024 Sep 27;16(9):e70308. doi: 10.7759/cureus.70308. eCollection 2024 Sep.

Abstract

Hereditary spherocytosis (HS) is a genetic disorder characterized by the presence of spherocytes, which are abnormally shaped red blood cells, leading to hemolytic anemia. While HS is not uncommon in hematology, it can present significant diagnostic and therapeutic challenges in its late stages, particularly when complicated by severe cholestasis. We report a case of a 48-year-old male presenting with jaundice and abdominal pain, initially diagnosed with cholecystolithiasis and moderate splenomegaly. Subsequent investigations confirmed HS through clinical observation and eosin-5'-maleimide (EMA) binding by flow cytometry. The patient exhibited severe jaundice (total bilirubin: 19.58 mg/dL) but no anemia. The complexity of his condition necessitated a multidisciplinary approach involving hematologists and gastroenterologists along with general medicine. This case underscores the importance of considering HS in the differential diagnosis of cholestasis and highlights the need for comprehensive diagnostic strategies to manage such complications effectively.

Keywords: eosin-5'-maleimide; hereditary spherocytosis; osmotic fragility test; sickling test; spleenomegaly.

Publication types

  • Case Reports