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Indolent Systemic Mastocytosis: An Incidental Diagnosis

Authors: Ayesha Khalid; Arfa Faiz; Alan Kaell;

Indolent Systemic Mastocytosis: An Incidental Diagnosis

Abstract

Indolent systemic mastocytosis (ISM) is the most prevalent subtype of systemic mastocytosis, characterized by a clinical course progressing over several years to decades. We present a case of a 57-year-old woman with symptoms of flushing and occasional dizziness who was diagnosed with ISM after a colon polyp biopsy revealed CD3-, CD20-, and CD25-positive atypical mast cell infiltrates. The patient was started on antihistamines with advice to avoid triggering factors. This case raises awareness about mast cell disorders. Clinicians should always keep these disorders in mind while evaluating a patient with nonspecific signs and symptoms involving multiple organ systems.

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Keywords

Internal medicine, RC31-1245

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selected citations
These citations are derived from selected sources.
This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Citations provided by BIP!
popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
BIP!Impulse provided by BIP!
0
Average
Average
Average
bronze