Murshid Areen Abdulelah, Al-Maghraby Hatim Q
Department of Pathology, King Abdulaziz University Hospital, Jeddah, Saudi Arabia.
Department of Pathology and Laboratory Medicine, King Saud Bin Abdulaziz University for Health Sciences, King Abdulaziz Medical City, Jeddah, Saudi Arabia.
Case Rep Pathol. 2018 May 2;2018:1082956. doi: 10.1155/2018/1082956. eCollection 2018.
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.
肠系膜硬纤维瘤(深部纤维瘤病)是一种罕见的间叶组织肿瘤。它们常被误诊,尤其是在既往有胃肠道间质瘤(GIST)切除史的情况下。免疫组织化学有助于鉴别这两种肿瘤。在本文中,我们介绍我们遇到的一例病例:一名3年前有GIST病史的患者发生了硬纤维瘤。这是沙特阿拉伯报道的首例GIST后发生硬纤维瘤的病例。我们通过比较硬纤维瘤和GIST的定义、临床表现、组织学特征、免疫组织化学染色、分子发病机制、预后及治疗,对这两种疾病进行了讨论。我们还讨论了GIST与硬纤维瘤后续发生之间的关系,并将我们的病例与文献中的病例报告进行了比较。