Wiley, American Journal of Hematology, 2(87), p. 191-193, 2011
DOI: 10.1002/ajh.22208
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A 54-year-old male was originally referred to our institution 2 years prior with a diagnosis of systemic mastocytosis (SM). Past medical history was significant for urticaria pigmentosa, which was diagnosed 15 years prior, and fatigue, diarrhea, and weight loss (similar to 10%), which were more recent in nature. In addition, a recent computed tomography (CT) scan revealed lymphadenopathy and hepatosplenomegaly.