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睾丸鞘膜多房性肿瘤作为罕见的睾丸旁囊腺瘤

A Paratesticular Multicystic Tumor of the Tunica Vaginalis Testis as Rare Paratesticular Cystadenoma.

作者信息

Draeger Desiree Louise, Kraeft Stine-Kathrein, Protzel Chris, Hakenberg Oliver W

机构信息

Department of Urology, University Rostock, Rostock, Germany.

出版信息

Urol Int. 2018;101(2):245-248. doi: 10.1159/000458159. Epub 2017 Feb 15.

Abstract

The cystadenoma of the testis and paratestis arising from an unequivocal oviduct-like structure, which is morphologically almost identical with those of the ovarian surface epithelium. These are very rare benign tumors of young adults. They present as asymptomatic cystic lesions. Bilateral paratesticular cystadenomas are strongly associated with von Hippel-Lindau syndrome and correlate with infertility. It is a neoplasm with low malignant potential. Most cystadenomas are benign but a few cases of malignant transformation of embryonic remnants have been reported in the appendix testis, including cases of adenocarcinoma, cystadenocarcinoma, and a low malignant müllerian-type epithelial tumor. We report the rare case of a 63-year-old man with a paratesticular multicystic cystadenoma of the male adnexa without association to von Hippel-Lindau disease.

摘要

睾丸和副睾的囊腺瘤起源于明确的输卵管样结构,其形态与卵巢表面上皮的结构几乎相同。这些是非常罕见的年轻成年人良性肿瘤。它们表现为无症状的囊性病变。双侧副睾囊腺瘤与冯·希佩尔-林道综合征密切相关,并与不育有关。它是一种恶性潜能较低的肿瘤。大多数囊腺瘤是良性的,但在睾丸附件中已有少数胚胎残余恶性转化的病例报道,包括腺癌、囊腺癌和低恶性苗勒管型上皮肿瘤。我们报告了一例罕见的63岁男性病例,其男性附件有副睾多囊性囊腺瘤,与冯·希佩尔-林道病无关。

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