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成熟睾丸畸胎瘤转移灶中伪装成胚胎性癌的血管肉瘤。

Angiosarcoma masquerading as embryonal carcinoma in the metastasis from a mature testicular teratoma.

作者信息

Sahoo Sunati, Ryan Christopher W, Recant Wendy M, Yang Ximing J

机构信息

Department of Pathology, Section of Hematology and Oncology, The University of Chicago, Chicago, IL, USA.

出版信息

Arch Pathol Lab Med. 2003 Mar;127(3):360-3. doi: 10.5858/2003-127-0360-AMAECI.

DOI:10.5858/2003-127-0360-AMAECI
PMID:12653585
Abstract

Sarcoma can arise within a germ cell tumor (GCT) from a malignant transformation of teratomatous elements or as late sequelae to radiation therapy. Angiosarcoma as a malignant component in testicular GCTs has rarely been reported and is often misdiagnosed as embryonal carcinoma. We report the case of a 23-year-old man with mature teratoma of the testis and retroperitoneal metastasis exhibiting components of mature teratoma intermingled with high-grade angiosarcoma. It is important to recognize the presence of a high-grade sarcomatous component within a GCT because of its aggressive clinical behavior and different response to therapy.

摘要

肉瘤可发生于生殖细胞肿瘤(GCT)内,由畸胎瘤成分的恶性转化引起,或作为放射治疗的晚期后遗症出现。血管肉瘤作为睾丸GCT的恶性成分鲜有报道,且常被误诊为胚胎性癌。我们报告了一例23岁男性病例,其睾丸成熟畸胎瘤伴腹膜后转移,肿瘤表现为成熟畸胎瘤成分与高级别血管肉瘤相互混杂。认识到GCT内存在高级别肉瘤成分很重要,因为其临床行为具有侵袭性,且对治疗的反应不同。

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Angiosarcoma masquerading as embryonal carcinoma in the metastasis from a mature testicular teratoma.成熟睾丸畸胎瘤转移灶中伪装成胚胎性癌的血管肉瘤。
Arch Pathol Lab Med. 2003 Mar;127(3):360-3. doi: 10.5858/2003-127-0360-AMAECI.
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引用本文的文献

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Primary pure angiosarcoma of the testis: a vanishingly rare malignancy. Case report and literature review.睾丸原发性单纯血管肉瘤:一种罕见的恶性肿瘤。病例报告及文献复习。
BMC Urol. 2020 Oct 31;20(1):175. doi: 10.1186/s12894-020-00747-7.
2
Primary angiosarcoma of the testis: report of a rare entity and review of the literature.睾丸原发性血管肉瘤:1例罕见病例报告并文献复习
Diagn Pathol. 2007 Jul 2;2:23. doi: 10.1186/1746-1596-2-23.