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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Bibliografiske detaljer
Main Authors: Mallya, Ketan P, Belurkar, Sushma, Kurian, Annamma, Rao, Laxmi, Singhania, Bikash
Format: Artigo
Sprog:Inglês
Udgivet: JCDR Research and Publications (P) Limited 2013
Fag:
Case Report
Online adgang: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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