Systemic Mastocytosis: Predominantly Involving the Bone, A Case Report

Systemic mastocytosis (SM) is a rare clonal disorder of mast cells that can range from chronic smouldering type to aggressive mast cell leukaemia. It presents with non–specific symptoms like urticaria pigmentosa, unexplained flushing, hypotension and abdominal cramps, which may lead to a misdiagnosi...

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Autors principals: Mallya, Ketan P, Belurkar, Sushma, Kurian, Annamma, Rao, Laxmi, Singhania, Bikash
Format: Artigo
Idioma:Inglês
Publicat: JCDR Research and Publications (P) Limited 2013
Matèries:
Case Report
Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC3843398/
https://ncbi.nlm.nih.gov/pubmed/24298498
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.7860/JCDR/2013/5669.3493
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