Lopez-Tomassetti Fernandez E M, Luis H Diaz, Malagon A Martin, Gonzalez I Arteaga, Pallares A Carrillo
Department of Gastrointestinal Surgery, University Hospital of Canary Islands, Ofra s/n. La Cuesta, La Laguna, Santa Cruz de Tenerife, Spain.
World J Gastroenterol. 2006 Jun 28;12(24):3938-43. doi: 10.3748/wjg.v12.i24.3938.
Inflammatory myofibroblastic tumors (IMTs) or inflammatory pseudotumors (IPs) have been extensively discussed in the literature. They are usually found in the lung and upper respiratory tract. However, reporting of cases involving the biliopancreatic region has increased over recent years. Immunohistochemical study of these lesions limited to the pancreatic head or distal bile duct seems to be compatible with those observed in a new entity called autoimmune pancreatitis, but usually intense fibrotic reaction (zonation) predominates producing a mass. When this condition is limited to the pancreatic head, the common bile duct might be involved by the inflammatory process and jaundice may occur often resembling adenocarcinoma of the pancreas. We have previously reported a case of IMT arising from the bile duct associated with autoimmune pancreatitis which is an extremely rare entity. Four years after Kaush-Whipple resection, radiological examination on routine follow-up revealed a tumor mass, suggesting local recurrence. Ultrasound-guided FNA confirmed our suspicious diagnosis. This present case, as others, suggests that persistent follow-up is necessary in order to prevent irreversible liver damage at this specific location.
炎性肌成纤维细胞瘤(IMTs)或炎性假瘤(IPs)在文献中已被广泛讨论。它们通常见于肺部和上呼吸道。然而,近年来涉及胆胰区域的病例报告有所增加。对局限于胰头或远端胆管的这些病变进行免疫组织化学研究,似乎与在一种称为自身免疫性胰腺炎的新疾病中观察到的情况相符,但通常强烈的纤维化反应(分区)占主导,形成肿块。当这种情况局限于胰头时,胆总管可能会受到炎症过程的影响,黄疸可能经常出现,常类似于胰腺癌。我们之前曾报告过一例起源于胆管并伴有自身免疫性胰腺炎的IMT病例,这是一种极其罕见的疾病。在进行Kaush-Whipple切除术后四年,常规随访的影像学检查发现一个肿瘤肿块,提示局部复发。超声引导下细针穿刺抽吸活检(FNA)证实了我们的可疑诊断。本病例与其他病例一样,表明为防止该特定部位出现不可逆的肝损伤,持续随访是必要的。