A child with acquired factor XIII deficiency: case report and literature review.

TitleA child with acquired factor XIII deficiency: case report and literature review.
Publication TypeJournal Article
Year of Publication2013
AuthorsKessel R, Hu C, Shore-Lesserson L, Rand J, Manwani D
JournalHaemophilia
Volume19
Issue6
Pagination814-26
Date Published2013 Nov
ISSN1365-2516
KeywordsChild, Factor XIII, Factor XIII Deficiency, Female, Fibrinolysin, Fibrinolytic Agents, Hematoma, Humans, Magnetic Resonance Imaging, Prognosis, Protein Subunits, Recombinant Proteins, Treatment Outcome
Abstract

Factor XIII (FXIII) deficiency is a rare bleeding disorder, which can result in life threatening hemorrhage. Rarer still is acquired FXIII deficiency, in which the disorder is due to autoantibodies that inhibit the factor. To describe one of the youngest reported patients with this condition. To discuss the challenges we encountered in monitoring response with the available assays. To review the literature and provide a review of all acquired FXIII cases. We present the case of our patient, a 9-year-old girl with acquired FXIII deficiency. We present a comprehensive review of all acquired FXIII deficiency cases reported globally in English, with focus on clinical presentation, diagnostic assays, treatment and prognosis. There is no current standard for therapy and measuring response to therapy can be complicated by limitations of assays in the presence of inhibitors. Clinicians should be aware of acquired FXIII deficiency as a potentially life threatening bleeding disorder even in young children. The case presented illustrates a young patient with acquired FXIII deficiency with a good clinical response to cryoprecipitate and difficulty in hemostasis monitoring utilizing clinically available assays.

DOI10.1111/hae.12145
Alternate JournalHaemophilia
PubMed ID23607876
Related Faculty: 
Jacob H. Rand, M.D.

Pathology & Laboratory Medicine 1300 York Avenue New York, NY 10065 Phone: (212) 746-6464
Surgical Pathology: (212) 746-2700