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Successful medical management of a neonate with spontaneous splenic rupture and severe hemophilia A
Journal article   Open access

Successful medical management of a neonate with spontaneous splenic rupture and severe hemophilia A

Sherif M Badawy, Jenna Rossoff, Sushmita Yallapragada, Robert I Liem and Anjali A Sharathkumar
Hematology/oncology and stem cell therapy, Vol.10(1), pp.29-32
03/2017
DOI: 10.1016/j.hemonc.2016.04.001
PMID: 27178624
url
https://doi.org/10.1016/j.hemonc.2016.04.001View
Published (Version of record) Open Access

Abstract

Splenic rupture in neonates is a rare event, usually occurring in the setting of underlying predisposing conditions. Here, we present the case of a term neonate who presented with worsening anemia in the setting of known hemolytic disease during the newborn period and was later found to have a spontaneous splenic rupture. He was subsequently diagnosed with severe hemophilia A, and was managed medically with recombinant factor VIII replacement therapy without any surgical intervention. This is the first reported case of a neonate who had spontaneous splenic rupture and severe hemophilia A, and underwent successful medical treatment without any surgical intervention.
Neonate Factor VIII deficiency Splenic rupture Hemophilia A

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