Literature DB >> 18082724

Splenic infarction due to concomitant hereditary spherocytosis and sickle cell trait.

Robin Yates Dulman1, George R Buchanan, Howard Ginsburg, Nancy R Fefferman, M Alba Greco, Dariusz Borys, Francine Blei.   

Abstract

Concomitant hereditary spherocytosis and sickle cell trait, although extremely rare, could potentially lead to splenic sequestration or infarction. We report here the first case of splenic infarction in a child with hereditary spherocytosis and sickle cell trait while flying on a commercial aircraft. The presence of hypoxia, hemoconcentrated erythrocytes, and sickle hemoglobin created the perfect environment for clinical sequelae.

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Year:  2007        PMID: 18082724     DOI: 10.1016/j.jpedsurg.2007.07.057

Source DB:  PubMed          Journal:  J Pediatr Surg        ISSN: 0022-3468            Impact factor:   2.545


  3 in total

Review 1.  An adolescent with hereditary spherocytosis who presented with splenic infarction.

Authors:  Lara Jones; Zafer Refai; Mike Linney
Journal:  BMJ Case Rep       Date:  2015-07-02

2.  Multiple splenic infarcts: unusual presentation of hereditary spherocytosis associated with acute Epstein-Barr virus infection.

Authors:  Aye Mon Thida; Ifeanyi Ilonzo; Pouyan Gohari
Journal:  BMJ Case Rep       Date:  2020-07-13

Review 3.  Splenic infarction after Epstein-Barr virus infection in a patient with hereditary spherocytosis: a case report and literature review.

Authors:  Zhongwu Ma; Zhejin Wang; Xiaodan Zhang; Haibo Yu
Journal:  BMC Surg       Date:  2022-04-09       Impact factor: 2.102

  3 in total

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