Acute aleukemic mast cell leukemia: Report of a case and review of the literature

[No authors listed] [No authors listed] Leuk Res Rep. 2022 Apr 6;17:100308. doi: 10.1016/j.lrr.2022.100308. eCollection 2022. Leuk Res Rep. 2022. PMID: 35832060 Free PMC article.

Abstract

Mast Cell Leukemia (MCL) is the rarest form of systemic mastocytosis, a rare group of neoplastic disease that result from clonal proliferation of mast cells and their accumulation in one or more organ systems. The diagnosis of MCL is made by meeting the World Health Organization (WHO) 2017 criteria. MCL is further subclassified as leukemic or aleukemic based on presence or absence of circulating mast cells in the peripheral blood and acute versus chronic based on presence or absence of findings indicative of impaired organ function due to mast cell infiltration. A 64-year-old Hispanic male presented with myalgia, diarrhea, urticarial rash, back pain, and fulminant disseminated intravascular coagulation. Bone marrow examination, supplemented by immunohistochemistry results, fulfilled the WHO criteria for the diagnosis of MCL. To the best of our knowledge, this is the first documented case of aleukemic acute MCL in a Hispanic patient.

Keywords: Acute; Aleukemic; Chronic; Hispanic; Leukemic; Mast cell leukemia; Therapy.

© 2020 The Author(s).

Conflict of interest statement

None of the authors have any conflict of interest to declare.