Case Study




S Rahar, S Marwah, S Singh

ABSTRACT: Sickle cell disease is one of the common hemoglobinopathies in the world affecting many organs including spleen. Splenomegaly in adult patients with sickle cell disease is very uncommon, however, in this case patient presented first time in adulthood with acute abdomen which is unusual.This case is presented to emphasize that, although rare, splenomegaly can persist in adults with sickle cell disease and can be associated with severe and even life-threatening splenic sequestration

KEY WORDS: cell disease,Haemoglobinopathies, Splenomegaly,Splenic sequestration


  1. Wintrobe clinical haematology. 13th ed;2013: 686-702.

  2. A,Kontras S et al .Splenomegaly with Hypersplenism in Sickle Cell Anemia Treated by Radiation—Case Report ;Paediatrics.1971;48(3)

  3. R, Rahman A et al. Fibrocongestive Splenomegaly in Sickle Cell Disease: A Distinct Clinicopathological Entity in the Eastern Province of Saudi Arabia. Am j Haemat.2005;180-185

  4. Moll S, Orringer EP et al.Case report: splenomegaly and splenic sequestration in an adult with sickle cell anemia.Am J Med Sci. 1996 Dec;312(6):299-302.

Basics and upadate on flow cytometry related research

IJMLR events

   Article are invited for

         Vol 6, Issue 2, 2021

  • Facebook - Black Circle
  • Google+ - Black Circle

Copyright © 2016 International Journal of Medical Laboratory Research. All right reserved