Management of hydrocephalus in infants with severe hemophilia A: report of 2 cases

Author:

Bergin Stephen M.12,Dunn Amy L.3,Smith Luke G. F.1,Drapeau Annie I.14

Affiliation:

1. Department of Neurosurgery;

2. Medical Scientist Training Program;

3. Nationwide Children’s Hospital Division of Hematology, Oncology & BMT; and

4. Nationwide Children’s Hospital Division of Pediatric Neurosurgery, The Ohio State University College of Medicine, Columbus, Ohio

Abstract

The authors report on the clinical course of two infants with severe hemophilia A (HA) and concomitant progressive hydrocephalus that required management with a ventriculoperitoneal shunt. The first child, with known HA, presented with a spontaneous intracranial hemorrhage and acquired hydrocephalus. He underwent cerebrospinal fluid diversion with a temporary external ventricular drain, followed by placement of a ventriculoperitoneal shunt. The second child had hydrocephalus secondary to a Dandy-Walker malformation and was diagnosed with severe HA during preoperative evaluation. He underwent placement of a ventriculoperitoneal shunt after progression of the hydrocephalus. The authors also review the treatment of hydrocephalus in patients with HA and describe the perioperative protocols used in their two cases. Treatment of hydrocephalus in infants with HA requires unique perioperative management to avoid complications.

Publisher

Journal of Neurosurgery Publishing Group (JNSPG)

Subject

General Medicine

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