You could be reading the full-text of this article now if you...

If you have access to this article through your institution,
you can view this article in

Spontaneous Epidural Hematoma in a Child With Inherited Factor XIII Deficiency

Farah, Roula A. MD, FAAP; Al Danaf, Jad Z. BS; Chahinian, Rita A. BS; Braiteh, Nabil T. BS; Al Ojaimi, Naim F. BS; Cairo, Andrea MD; Farhat, Hussein MD; Mantoura, Joseph R. MD

Journal of Pediatric Hematology/Oncology:
doi: 10.1097/MPH.0b013e31828e52b6
Original Articles
Abstract

We report the case of a 2-year-old Lebanese male child, known to have congenital factor XIII (FXIII) deficiency, who presented to the emergency department with somnolence and projectile vomiting without any head trauma. He has been on a prophylactic dose of 10 IU/kg of FXIII concentrate every 4 weeks since birth, but he missed his last 2 doses due to shortage of supply. Imaging studies showed an epidural hematoma with a midline shift. The child was started on 20 IU/kg of FXIII replacement, and a left parietal craniotomy was performed immediately. He tolerated the surgery well with an uneventful postoperative course. Previous DNA analysis carried out for the family members detected a small deletion (c.1475-1476delGA) in exon 12 in this child and his eldest brother. This mutation has been previously reported once in another Lebanese child with FXIII deficiency who presented with spontaneous splenic rupture. To the best of our knowledge, this is the first case of acute nontraumatic spontaneous epidural hematoma in a child with congenital FXIII deficiency. Furthermore, patients on FXIII replacement therapy have less bleeding events, thus lifelong adherence to the prophylaxis is essential to decrease the morbidities and the mortalities associated with FXIII deficiency, most notably intracranial hemorrhages.

Author Information

Departments of *Pediatrics

Laboratory Medicine

§Neurosurgery, University Medical Center-Rizk Hospital, Beirut, Lebanon

Angelo Bianchi Bonomi Hemophilia and Thrombosis Center, U.O.S. Dipartimentale per la, Diagnosi e la Terapia delle Coagulopatie, Fondazione IRCCS Cà Granda — Ospedale Maggiore, Policlinico, and Luigi Villa Foundation, Milan, Italy

The authors declare no conflict of interest.

Reprints: Roula A. Farah, MD, FAAP, Department of Pediatrics, University Medical Center-Rizk Hospital, Zahar Street, Achrafieh, 1107-2030 Beirut, Lebanon (e-mail: roula.fs@dm.net.lb).

Received September 11, 2012

Accepted February 20, 2013

Copyright © 2014 Wolters Kluwer Health, Inc. All rights reserved.