生殖道外生殖细胞瘤2例报告。

IF 0.9 Q4 ONCOLOGY
Rare Tumors Pub Date : 2021-06-30 eCollection Date: 2021-01-01 DOI:10.1177/20363613211029487
Mousa Elkhaldi, Ahamd Moayad Naser, Yazan AlHalaseh, Maysa Al-Hussaini
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引用次数: 2

摘要

生殖细胞肿瘤是一类异质性肿瘤,主要表现为局部或转移性性腺肿瘤。这些肿瘤最初很少出现在性腺外部位,包括胃肠道。我们报告了两名年轻男性患者,他们表现出由十二指肠肿块病变引起的非特异性胃肠道症状。病理证实为生殖细胞瘤;一种不熟悉的生殖细胞肿瘤的初始表现。在这两个病例中,在确诊为性腺外生殖细胞肿瘤后,分别在第一个和第二个病例中发现了以睾丸肿块和烧伤肿瘤合并微石症的形式存在的性腺肿瘤的证据。每位患者的临床过程和结果都强调了高度怀疑、及时诊断和适当管理的重要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Extragonadal germ cell tumor, a report of two cases presenting in the gastrointestinal tract.

Extragonadal germ cell tumor, a report of two cases presenting in the gastrointestinal tract.

Extragonadal germ cell tumor, a report of two cases presenting in the gastrointestinal tract.

Extragonadal germ cell tumor, a report of two cases presenting in the gastrointestinal tract.

Germ cell tumors are a heterogeneous group of tumors that can present primarily as gonadal tumors in either a localized or metastatic pattern. Rarely these tumors can initially present at extra-gonadal locations, including the gastrointestinal tract. We report two young male patients who presented with nonspecific gastrointestinal symptoms caused by a mass lesion involving the duodenum. Pathologically, both were confirmed to be germ cell tumors; an unfamiliar initial presentation of germ cell tumors. In both cases, evidence of pre-existing gonadal tumor in the form of a testicular mass and a burned-out tumor with microlithiasis, in the first and second cases, respectively was detected following the confirmed diagnosis of extra-gonadal germ cell tumor. Each patient's clinical course and outcome emphasizes the importance of a high index of suspicion, timely diagnosis, and appropriate management.

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来源期刊
Rare Tumors
Rare Tumors ONCOLOGY-
CiteScore
1.50
自引率
0.00%
发文量
15
审稿时长
15 weeks
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