Two cases of concomitant acquired aplastic anemia and systemic mastocytosis.

Abstract:

:Reactive bone marrow mast cells reliably lack the morphologic, immunophenotypic, and molecular features of systemic mastocytosis (SM). We report two unusual cases of acquired aplastic anemia (AA) in which multifocal aggregates of bone marrow mast cells fulfilled morphologic and immunophenotypic criteria for SM according to the World Health Organization 2008 classification. In the absence of clinical symptoms attributable to SM, the patients were treated with immunosuppressive therapy directed towards AA. Clinical follow-up and subsequent bone marrow examination revealed no evidence of overt SM in either patient. These cases represent, to our knowledge, the first reported instances in which criteria for SM have been fulfilled in the presence of AA. However, given the clinical courses followed by our patients, the incidental identification of mast cell lesions consistent with indolent SM may be of uncertain significance in the setting of AA.

journal_name

Hum Pathol

journal_title

Human pathology

authors

Golardi N,Sramek JE,Myers JB,Saffer H,George TI,Czuchlewski DR

doi

10.1016/j.humpath.2013.08.002

subject

Has Abstract

pub_date

2014-02-01 00:00:00

pages

417-20

issue

2

eissn

0046-8177

issn

1532-8392

pii

S0046-8177(13)00334-1

journal_volume

45

pub_type

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