Subsequent Development of Desmoid Tumor after a Resected Gastrointestinal Stromal Tumor

Autor:	Areen Abdulelah Murshid, Hatim Q. Almaghraby
Jazyk:	angličtina
Rok vydání:	2018
Předmět:	Pathology medicine.medical_specialty GiST business.industry Mesenchymal stem cell Molecular pathogenesis Case Report General Medicine digestive system diseases Resection body regions 03 medical and health sciences 0302 clinical medicine medicine.anatomical_structure 030220 oncology & carcinogenesis medicine lcsh:Pathology Immunohistochemistry 030211 gastroenterology & hepatology Deep Fibromatosis Stromal tumor Mesentery business neoplasms lcsh:RB1-214
Zdroj:	Case Reports in Pathology, Vol 2018 (2018) Case Reports in Pathology
ISSN:	2090-6781
Popis:	Desmoid tumors (deep fibromatosis) of the mesentery are rare mesenchymal tumors. They are often misdiagnosed, especially with a previous history of resection for gastrointestinal stromal tumor (GIST). Immunohistochemistry can help differentiate between these two tumors. In this article, we present a case we had encountered: a Desmoid tumor developing in a patient with a history of GIST 3 years ago. It is the first case of GIST with subsequent development of Desmoid tumor to be reported in Saudi Arabia. We discuss the two entities of Desmoid tumor and GIST by comparing their definitions, clinical presentations, histological features, immunohistochemistry stains, molecular pathogenesis, prognosis, and treatment. We also discuss the relationship between GIST and the subsequent development of Desmoid tumors and compare our case with case reports in literature.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31b77cbef72f45fa57acd77f5e6f1d50 https://doaj.org/article/457b9210ea9749acb094a58720fdf7f6 Zobrazit plný text záznamu Plný text ve formátu PDF Plný text ve formátu HTML
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