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原发性胆道黑色素瘤:1例报告并文献复习

Primary biliary tract melanoma: Report of a case and review of the literature.

作者信息

Smith Nathaniel E, Taube Janis M, Warczynski Tam M, Collier Kevin D, Pawlik Timothy M

机构信息

Department of Pathology, The Johns Hopkins Hospital, 600 North Wolfe Street, Baltimore, MD 21287, United States.

出版信息

Int J Surg Case Rep. 2012;3(9):441-4. doi: 10.1016/j.ijscr.2012.05.008. Epub 2012 May 24.

Abstract

INTRODUCTION

Primary melanoma of the bile duct is extremely rare with only nine cases of primary melanoma of the bile duct reported in the literature.

PRESENTATION OF CASE

A 55-year-old previously healthy gentleman developed increasing jaundice over several months and subsequently underwent an ERCP with stone extraction. Cytology brushings in an area of a distal stricture in the bile duct were concerning for cholangiocarcinoma. The patient was referred to our institution and underwent a pancreaticoduodenectomy. The surgical specimen showed a single 4.5cm polypoid lesion located in the bile duct. A diagnosis of melanoma was rendered after immunohistochemical studies on the tumor demonstrated positivity for melanoma markers. Follow-up of the patient with skin, ocular, and lymph node exams showed no evidence of melanoma. A PET scan 4 and 10 months post-surgery failed to reveal either a primary skin lesion or other sites of metastases.

DISCUSSION

The vast majority of melanomas of the bile duct represent metastases from a cutaneous source and tend to present as multiple flat pigmented lesions. Conversely, cases of primary bile duct melanoma are characterized by a distinct gross morphology consisting of a solitary intraluminal polypoid lesion attached by a pedicle with no other identifiable primary lesion. Other supporting criteria include absence of other involved sites and presence of an in situ junctional component.

CONCLUSION

Given the clinical history, gross findings, and lack of a primary cutaneous site or other demonstrable metastases, this patient likely represents the tenth reported case of primary biliary tract melanoma.

摘要

引言

胆管原发性黑色素瘤极为罕见,文献中仅报道过9例胆管原发性黑色素瘤。

病例介绍

一名55岁既往健康的男性在数月内黄疸进行性加重,随后接受了内镜逆行胰胆管造影术(ERCP)并取石。胆管远端狭窄处的细胞学刷检结果提示胆管癌。该患者被转诊至我院并接受了胰十二指肠切除术。手术标本显示胆管内有一个4.5厘米的息肉样病变。对肿瘤进行免疫组化研究后诊断为黑色素瘤,结果显示黑色素瘤标志物呈阳性。对患者进行皮肤、眼部和淋巴结检查的随访未发现黑色素瘤迹象。术后4个月和10个月的正电子发射断层扫描(PET)均未发现原发性皮肤病变或其他转移部位。

讨论

胆管黑色素瘤绝大多数为皮肤来源转移,往往表现为多个扁平色素沉着病变。相反,原发性胆管黑色素瘤的特征是具有独特的大体形态,由一个带蒂的孤立腔内息肉样病变组成,无其他可识别的原发性病变。其他支持标准包括无其他受累部位以及存在原位交界成分。

结论

鉴于该患者的临床病史、大体检查结果以及无原发性皮肤部位或其他可证实的转移,该患者可能是报道的第10例原发性胆道黑色素瘤。

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