Hereditary spherocytosis in children: profile and post-splenectomy outcome

Indian Pediatr. 2014 Feb;51(2):139-41. doi: 10.1007/s13312-014-0348-5.

Abstract

Objective: To describe profile of 82 children with hereditary spherocytosis diagnosed over a period of 27 years (1985-2011) from a single center.

Methods: Retrospective analyses of case records.

Results: The mean (SD) age at diagnosis was 6.7 (2.8) years; 7 (8.5%) were diagnosed in infancy. Pallor (100%), icterus (67%), undocumented fever (28%), splenomegaly (96%) and hepatomegaly (73%) were the most frequent findings. Cholelithiasis was observed in 26%. Twenty-six (32%) underwent splenectomy and were followed for a median duration of 4.5 years. Two (7.7%) children developed post-splenectomy sepsis.

Conclusion: Anemia, hepato-splenomegaly and jaundice are commonest clinical features of hereditary spherocytosis. Post-splenectomy sepsis is uncommon.

MeSH terms

  • Adolescent
  • Ankyrins / deficiency*
  • Child
  • Child, Preschool
  • Female
  • Humans
  • India
  • Infant
  • Male
  • Postoperative Complications
  • Retrospective Studies
  • Spherocytosis, Hereditary / diagnosis
  • Spherocytosis, Hereditary / surgery*
  • Splenectomy*
  • Treatment Outcome

Substances

  • Ankyrins

Supplementary concepts

  • Spherocytosis, Type 1