Epithelioid inflammatory myofibroblastic sarcoma
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Epithelioid inflammatory myofibroblastic sarcoma, abbreviated EIMS, is a rare malignant tumour.[1]
General
- An aggressive tumour - related inflammatory myofibroblastic tumour.<ref name=pmid27460384<{{Cite journal | last1 = Yu | first1 = L. | last2 = Liu | first2 = J. | last3 = Lao | first3 = IW. | last4 = Luo | first4 = Z. | last5 = Wang | first5 = J. | title = Epithelioid inflammatory myofibroblastic sarcoma: a clinicopathological, immunohistochemical and molecular cytogenetic analysis of five additional cases and review of the literature. | journal = Diagn Pathol | volume = 11 | issue = 1 | pages = 67 | month = Jul | year = 2016 | doi = 10.1186/s13000-016-0517-z | PMID = 27460384 }}</ref>
See also
References
- ↑ Mariño-Enríquez, A.; Wang, WL.; Roy, A.; Lopez-Terrada, D.; Lazar, AJ.; Fletcher, CD.; Coffin, CM.; Hornick, JL. (Jan 2011). "Epithelioid inflammatory myofibroblastic sarcoma: An aggressive intra-abdominal variant of inflammatory myofibroblastic tumor with nuclear membrane or perinuclear ALK.". Am J Surg Pathol 35 (1): 135-44. doi:10.1097/PAS.0b013e318200cfd5. PMID 21164297.