1,040
Views
1
CrossRef citations to date
0
Altmetric
HEMOGLOBINOPATHY

Splenic enlargement in adults with homozygous sickle cell disease: the Jamaican experience

, &
Pages 46-49 | Published online: 18 Jul 2013

References

  • De Ceulaer K, Serjeant GR. Acute splenic sequestration in Jamaican adults with homozygous sickle cell disease: a role of alpha thalassaemia. Br J Haematol. 1991;77:563–4.
  • Koduri PR. Acute splenic sequestration crisis in adults with sickle cell anemia. Am J Hematol. 2007;82:174–5.
  • Moll S, Orringer EP. Case report: splenomegaly and splenic sequestration in an adult with sickle cell anemia. Am J Med Sci. 1996;312:299–302.
  • Claster S, Vichinsky E. First report of reversal of organ dysfunction in sickle cell anemia by the use of hydroxyurea: splenic regeneration. Blood. 1996;88:1951–3.
  • Campbell PJ, Olatunji PO, Ryan KE, Davies SC. Splenic regrowth in sickle cell anaemia following hypertransfusion. Br J Haematol. 1997;96:77–9.
  • Wethers DL, Grover R. Reversibility of splenic function by transfusion in two young adults with sickle cell anemia. Am J Pediatr Hematol Oncol. 1987;9:209–11.
  • Inati A, Jradi O, Tarabay H, Moallem H, Rachkidi Y, El Accaoui R, et al. Sickle cell disease: the Lebanese experience. Int J Lab Hematol. 2007;29:399–408.
  • Jama AH, Salem AH, Dabbous IA. Massive splenic infarction in Saudi patients with sickle cell anemia: a unique manifestation. Am J Hematol. 2002;69:205–9.
  • Haghshenass M, Ismail-Beigi F, Clegg JB, Weatherall DJ. Mild sickle-cell anaemia in Iran associated with high levels of fetal haemoglobin. J Med Genet. 1977;14:168–71.
  • Habibi A, Khellaf M, Bachir D, Schaeffer A, Galacteros F, Godeau B. [Acute splenic sequestration: a rare and severe complication of sickle cell anemia in adults. A case report]. La Revue de medecine interne/fondee 2005;26:339–42.
  • Singh S, Singh DK, Gupta R, Nigam S, Singh T. Persistent splenomegaly in an adult female with homozygous sickle cell anemia. Hematology (Amsterdam, Netherlands) 2006;11:63–5.
  • Pearson HA. Sickle cell anemia and severe infections due to encapsulated bacteria. J Infect Dis. 1977;136 (Suppl):S25–30.
  • Higgs DR, Aldridge BE, Lamb J, Clegg JB, Weatherall DJ, Hayes RJ, et al. The interaction of alpha-thalassemia and homozygous sickle-cell disease. N Engl J Med. 1982;306:1441–6.
  • Ballas SK, Gay RN, Chehab FF. Is Hb A2 elevated in adults with sickle-alpha-thalassemia (beta(S)/beta(S); -alpha/-alpha)? Hemoglobin. 1997;21:405–50.
  • Hagar W, Vichinsky E. Advances in clinical research in sickle cell disease. Br J Haematol. 2008;141:346–56.
  • Okpala I. The intriguing contribution of white blood cells to sickle cell disease – a red cell disorder. Blood Rev. 2004;18:65–73.
  • Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT. The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia. Am J Hematol. 1986;21:383–95.
  • Padmos MA, Roberts GT, Sackey K, Kulozik A, Bail S, Morris JS, et al. Two different forms of homozygous sickle cell disease occur in Saudi Arabia. Br J Haematol. 1991;79:93–8.
  • Sarma PS. Acute splenic sequestration crisis in a young woman with homozygous sickle cell anaemia. Postgrad Med. J. 1989;65:105–7.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.