| Literature DB >> 31567270 |
Juan G Ripoll1, Matthew J Ritter1,2,3, Thomas B Comfere1,2, Mark M Smith1,3, Hartzell V Schaff4, George D Gilkey1,3, Matthew A Warner1,2.
Abstract
Systemic mastocytosis (SM) is a rare clinical condition resulting from a clonal proliferation of abnormal mast cells. The clinical presentation may vary from mild cutaneous manifestations to aggressive systemic symptoms including intermittent episodes of anaphylaxis. We present a case of a 69-year-old male with abrupt and recurrent episodes of anaphylaxis with refractory distributive shock following cardiac surgery with cardiopulmonary bypass. Following a complex postoperative course, a bone marrow biopsy ultimately confirmed the diagnosis. Although rare, SM should be considered in the differential diagnosis of postoperative patients with unexplained and recurrent episodes of distributive shock.Entities:
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Year: 2019 PMID: 31567270 PMCID: PMC6856421 DOI: 10.1213/XAA.0000000000001093
Source DB: PubMed Journal: A A Pract ISSN: 2575-3126