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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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| 主要な著者: | , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
JCDR Research and Publications (P) Limited
2013
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| 主題: | |
| オンライン･アクセス: | 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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