Hemophilia A

Hemophilia A is the most common form of hemophilia (see this term) characterized by spontaneous or prolonged hemorrhages due to factor VIII deficiency.

Splenic rupture

A breach of the capsule of the spleen.


Total: 4

                       


(per page)
PMID (PMCID)
26157867
(4435321)
 OTHER
Delayed Presentation of Splenic Rupture After Endoscopy in a Patient With Hemophilia A: Case Report and Review of the Literature.
Mazulis A, Lakha A, Qazi B, Shapiro A.
ACG Case Rep J. 2014;1(4):175-7.
We present, to our knowledge, a case of the longest reported delay in presentation of post-colonoscopy splenic rupture and the first in a patient with hemophilia A.
26157867
(4435321)
 OTHER
Delayed Presentation of Splenic Rupture After Endoscopy in a Patient With Hemophilia A: Case Report and Review of the Literature.
Mazulis A, Lakha A, Qazi B, Shapiro A.
ACG Case Rep J. 2014;1(4):175-7.
Delayed Presentation of Splenic Rupture After Endoscopy in a Patient With Hemophilia A: Case Report and Review of the Literature.
1522472
 MALE Child
Nonsurgical therapy of splenic rupture in a hemophiliac.
Jona JZ, Cox-Gill J.
J Pediatr Surg. 1992;27(4):523-4.
A boy with known hemophilia A sustained severe blunt abdominal trauma that caused major splenic rupture and hypovolemia.
6823613
 MALE Adult
Hemophilic splenic rupture without thrombocytosis.
Krauss JS, Hahn DA.
South Med J. 1983;76(2):272.
Spontaneous splenic rupture in hemophilia A is an uncommon occurrence which is difficult to diagnose.