Yamaga Shinya, Kugiyama Naotaka, Hashigo Shunpei, Nagaoka Katsuya, Yamada Rin, Ushijima Shinya, Uramoto Yukiko, Yoshinari Motohiro, Naoe Hideaki, Tanaka Yasuhito
Department of Gastroenterology and Hepatology, Faculty of Life Sciences, Kumamoto University.
Department of Gastroenterology and Hepatology, Kumamoto Kenhoku Hospital.
Nihon Shokakibyo Gakkai Zasshi. 2024;121(10):842-850. doi: 10.11405/nisshoshi.121.842.
Biliary amputation neuroma is a rare benign tumor that develops due to the peribiliary dissection of nerve fibers during cholecystectomy, a common bile duct surgery, or lymph node dissection performed in gastric cancer surgery. We report a case of amputation neuroma that presented a challenging differential diagnosis from perihilar cholangiocarcinoma. A 64-year-old man, who had undergone open cholecystectomy 30 years ago, was incidentally found to have a bile duct tumor during computed tomography (CT) following surgery for renal cell carcinoma. He had no specific symptoms, and blood test results showed only a slight elevation in alkaline phosphatase levels. Contrast-enhanced CT revealed a 10-mm solid tumor with contrast effect in the common bile duct. On cholangiography, the tumor appeared as a protruding lesion with a smooth surface unilaterally. Given the atypical findings suggestive of cholangiocarcinoma, three bile duct biopsies were performed. Pathological examination did not rule out adenocarcinoma. The patient opted for surgery;however, an intraoperative rapid histological examination confirmed a benign disease, thereby avoiding extensive surgery. Consequently, a minimally invasive bile duct resection was performed. Postoperative histopathological examination revealed the tumor to be an amputation neuroma. Biliary amputation neuromas are characterized as unilateral protruding lesions with contrast effect or benign strictures. If such findings are observed in a patient with a history of surgery around the bile duct, the possibility of an amputation neuroma should be considered. However, completely ruling out malignancy preoperatively, even when suspecting amputation neuroma, can be challenging;therefore, considering surgery to achieve a definitive diagnosis is reasonable. During surgery, a rapid intraoperative histological examination is useful to avoid extensive procedures. In conclusion, diagnosing an amputation neuroma before surgery can be difficult, as it can mimic malignant tumors such as bile duct cancers. In this case, although a preoperative diagnosis of amputation neuroma was not feasible, performing a rapid intraoperative pathological examination helped avoid extensive surgery.
胆管截肢性神经瘤是一种罕见的良性肿瘤,它是在胆囊切除术、胆总管手术或胃癌手术中的淋巴结清扫术期间,因胆管周围神经纤维的解剖而形成的。我们报告一例截肢性神经瘤病例,该病例在与肝门周围胆管癌的鉴别诊断上颇具挑战性。一名64岁男性,30年前接受了开腹胆囊切除术,在肾细胞癌手术后的计算机断层扫描(CT)检查中偶然发现胆管肿瘤。他没有特定症状,血液检查结果仅显示碱性磷酸酶水平略有升高。增强CT显示胆总管内有一个10毫米的实性肿瘤,有强化效应。在胆管造影中,肿瘤表现为单侧表面光滑的突出病变。鉴于提示胆管癌的非典型表现,进行了三次胆管活检。病理检查未排除腺癌。患者选择手术;然而,术中快速组织学检查证实为良性疾病,从而避免了广泛手术。因此,进行了微创胆管切除术。术后组织病理学检查显示肿瘤为截肢性神经瘤。胆管截肢性神经瘤的特征为具有强化效应的单侧突出病变或良性狭窄。如果在有胆管周围手术史的患者中观察到这些表现,应考虑截肢性神经瘤的可能性。然而,即使怀疑是截肢性神经瘤,术前完全排除恶性肿瘤也可能具有挑战性;因此,考虑手术以获得明确诊断是合理的。在手术过程中,术中快速组织学检查有助于避免进行广泛的手术操作。总之,术前诊断截肢性神经瘤可能很困难,因为它可能模仿胆管癌等恶性肿瘤。在本病例中,虽然术前诊断截肢性神经瘤不可行,但进行术中快速病理检查有助于避免广泛手术。