侵袭性肝门炎性肌纤维母细胞瘤合并肝门胆管原位癌。

Bum-Soo Kim, Sun-Hyung Joo, Gou-Young Kim, Kwang-Ro Joo
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引用次数: 7

摘要

胆道炎性肌纤维母细胞瘤(IMT)极为罕见,通常为良性,但也有可能发生恶性变化。在术前影像学检查中鉴别诊断这种病变和其他恶性疾病是非常困难的。因此,IMT的最终诊断可能取决于手术中或手术后的病理检查。我们治疗了一位63岁的女性,她在怀疑肝门胆管癌的情况下接受了右肝切除术并尾状叶切除术。术中冰冻活检显示原位癌,胆管切除缘可见间质细胞。术后住院期间除轻微胆漏外一切顺利。术后第4个月,患者出现黄疸、腹水和胸腔积液。计算机断层图像显示肝门有肿块样病变伴门静脉血栓形成和右胸壁肿块。切除活检后,病理报告为恶性梭形细胞瘤,提示侵袭性IMT。尽管得到了最好的支持治疗,她的病情迅速恶化,于术后第5个月死亡。对于本病复发及浸润的原因,需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Aggressive hilar inflammatory myofibroblastic tumor with hilar bile duct carcinoma in situ.

Inflammatory myofibroblastic tumor (IMT) of the biliary tree is extremely rare and is generally a benign condition, though malignant change is possible. Making a differential diagnosis between this lesion and other malignant conditions is very difficult on preoperative imaging studies. Hence, the final diagnosis of IMT may be made during or after operation depending on the pathologic examination. We treated a 63-year-old woman who received right hepatectomy with caudate lobectomy under the suspicion of hilar cholangiocarcinoma. Frozen biopsy during the operation showed carcinoma in situ and there were stromal cells in the bile duct's resection margins. The postoperative hospital course was uneventful except for minor bile leakage. At postoperative month 4, she developed jaundice, ascites and pleural effusion. Computed tomography images showed a mass-like lesion in the porta hepatis with portal vein thrombosis and a right chest wall mass. Excisional biopsy was done and the pathology report was malignant spindle cell tumor suggestive of an aggressive form of IMT. Her condition rapidly deteriorated regardless of the best supportive care and she expired at postoperative month 5. Further investigation is necessary to clarify the reasons for recurrence and infiltration of this disease.

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