肝门胆道囊腺瘤伴IgG4升高1例。

IF 1.1 Q2 MEDICINE, GENERAL & INTERNAL Intractable & rare diseases research Pub Date : 2022-08-01 DOI:10.5582/irdr.2022.01076
Zushun Chen, Haiming Lu, Jingxuan Xu, Liang Ma
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引用次数: 0

摘要

肝门部胆管胆管细胞腺瘤少见,同时IgG4升高极为罕见。这种情况在文献中未见报道。尽管如此,本病例涉及肝门胆道囊腺瘤伴IgG4水平升高。一名66岁男性因小便呈深茶色就诊于本院。术前影像学检查提示肝门胆管癌。本病例说明术前诊断肺门良性病变的困难和两种合并良性病变的罕见。争论的焦点是这个病例应该用手术还是激素治疗。
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A case of hilar biliary cystadenoma with elevated IgG4 levels.

Cholangiocytic adenoma in the hilar bile duct is rare, and elevated IgG4 at the same time is extremely rare. This situation has not been reported in the literature. Nonetheless, the current case involved hilar biliary cystadenoma with elevated IgG4 levels. A 66-year-old man presented at this hospital with dark tea-colored urine. Preoperative imaging studies suggested hilar cholangiocarcinoma. This case demonstrates the difficulty of preoperative diagnosis of benign hilar lesions and the rarity of two combined benign lesions. A point of contention is whether this case should be treated with surgery or hormone therapy.

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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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