Inherited ADAMTS13 deficiency: unique presentation and treatment.

Pediatr Blood Cancer

Department of Pediatric Hematology/Oncology, Gundersen Lutheran Health System, La Crosse, Wisconsin, USA.

Published: May 2008

A 3-year-old male presented with severe thrombocytopenia and microangiopathic hemolytic anemia in conjunction with severe bilateral otitis media. After laboratory analysis, a diagnosis of inherited ADAMTS13 deficiency was proven. Rather than treating with prophylactic fresh frozen plasma, to date the patient has been successfully treated with single-donor, directed plasma infusions in response to early signs of relapse. It may be reasonable to consider observational and reactive care rather than prophylactic care in some cases of inherited ADAMTS13 deficiency.

Download full-text PDF

Source
http://dx.doi.org/10.1002/pbc.21474DOI Listing

Publication Analysis

Top Keywords

inherited adamts13
12
adamts13 deficiency
12
deficiency unique
4
unique presentation
4
presentation treatment
4
treatment 3-year-old
4
3-year-old male
4
male presented
4
presented severe
4
severe thrombocytopenia
4

Similar Publications

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!