Martín Malagón Antonio, López-Tomassetti Fernández Eudaldo, Arteaga González Iván, Carrillo Pallarés Angel, Díaz Luis Hermogenes
Department of General Surgery, Hospital Universitario de Canarias, Tenerife, Canary Islands, Spain.
Pancreatology. 2006;6(1-2):145-54. doi: 10.1159/000090256. Epub 2005 Dec 13.
Inflammatory myofibroblastic tumor (IMT) or inflammatory pseudotumor has been described in various organs such as the liver, intestinal tract, spleen, kidney, bladder, lung, peritoneum and heart. However, its appearance in the periampullary region is uncommon and has rarely been reported in the literature. It is characterized histologically by myofibroblastic cell proliferation together with a mixed inflammatory infiltrate that clinically and radiologically mimics a malignant tumor. We report a case of IMT located in the distal common bile duct of a 51-year-old woman. She underwent Whipple resection with the initial diagnosis of cholangiocarcinoma; the pathologic diagnosis of the tumor was IMT of the distal bile duct associated with lymphoplasmacytic sclerosing pancreatitis. Referring to previously reported cases, suspected diagnosis of a malignant tumor made surgical excision the primary choice for symptom relief and in order to obtain a definitive diagnosis. IMT relationship with lymphoplasmacytic sclerosing pancreatitis is discussed.
炎性肌成纤维细胞瘤(IMT)或炎性假瘤已在肝脏、肠道、脾脏、肾脏、膀胱、肺、腹膜和心脏等多种器官中被描述。然而,其在壶腹周围区域的表现并不常见,文献中鲜有报道。其组织学特征为肌成纤维细胞增殖以及混合性炎性浸润,在临床和放射学上类似于恶性肿瘤。我们报告一例位于一名51岁女性胆总管远端的IMT病例。她最初被诊断为胆管癌并接受了惠普尔手术;肿瘤的病理诊断为远端胆管IMT伴淋巴浆细胞性硬化性胰腺炎。参考既往报道的病例,疑似恶性肿瘤的诊断使得手术切除成为缓解症状和获得明确诊断的主要选择。文中讨论了IMT与淋巴浆细胞性硬化性胰腺炎的关系。