Bashir Muhammad Rizwan, Al Sohaibani Mohammed Omar, Al-Rikabi Ammar Cherkess
Department of Histopathology and Cytology, Dallah Hospital, Riyadh, Saudi Arabia.
Department of Pathology, College of Medicine King Saud University, Riyadh, Saudi Arabia.
Oman Med J. 2018 May;33(3):250-252. doi: 10.5001/omj.2018.45.
Inflammatory myofibroblastic tumor (IMT) is reported virtually in every anatomic location of the body, but most cases are commonly identified in the mesentery and omentum. The etiology of this tumor is unclear with many suggestions of viral, inflammatory, or oncogenic mutational factors that establish it as a clonal neoplasm. Clinical and laboratory workup, including roentgenography, is not usually helpful to reach a pre- or intraoperative diagnosis. Histopathology and immunohistochemistry of the resected specimen provides a definitive answer by the exclusion of a close clinical differential diagnosis of gastrointestinal stromal tumor and many lookalikes. Complete surgical excision with clear margins is the mainstay of treatment. Rare cases have been seen involving the appendix. To the best of our knowledge, only 11 confirmed cases of purely appendiceal IMT have been published in the literature to date.
炎症性肌纤维母细胞瘤(IMT)几乎在身体的每个解剖部位都有报道,但大多数病例常见于肠系膜和大网膜。该肿瘤的病因尚不清楚,有许多关于病毒、炎症或致癌突变因素的推测,这些因素将其确立为一种克隆性肿瘤。包括X线摄影在内的临床和实验室检查通常无助于进行术前或术中诊断。切除标本的组织病理学和免疫组织化学检查通过排除胃肠道间质瘤和许多相似疾病的密切临床鉴别诊断,提供了明确的答案。手术切缘清晰的完整手术切除是主要的治疗方法。阑尾受累的病例较为罕见。据我们所知,迄今为止,文献中仅发表了11例确诊的单纯阑尾IMT病例。