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本文引用的文献

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A rare case of serous papillary cystadenocarcinoma of the testis.一例罕见的睾丸浆液性乳头状囊腺癌。
J Androl. 2010 Sep-Oct;31(5):434-6. doi: 10.2164/jandrol.109.009167. Epub 2010 Feb 4.
2
Serous papillary adenocarcinoma of the rete testis: unusual ultrasonography and pathological findings.睾丸网浆液性乳头状腺癌:不寻常的超声检查及病理表现
J Cancer Res Ther. 2007 Jan-Mar;3(1):37-9. doi: 10.4103/0973-1482.31970.
3
Selected other problematic testicular and paratesticular lesions: rete testis neoplasms and pseudotumors, mesothelial lesions and secondary tumors.其他选定的有问题的睾丸和睾丸旁病变:睾丸网肿瘤和假瘤、间皮病变及继发性肿瘤。
Mod Pathol. 2005 Feb;18 Suppl 2:S131-45. doi: 10.1038/modpathol.3800314.
4
Serous borderline tumors of the ovary: a long-term follow-up study of 137 cases, including 18 with a micropapillary pattern and 20 with microinvasion.卵巢浆液性交界性肿瘤:137例长期随访研究,其中18例具有微乳头模式,20例有微浸润。
Am J Surg Pathol. 2002 Sep;26(9):1111-28. doi: 10.1097/00000478-200209000-00002.
5
Serous borderline tumor of the paratestis: a report of seven cases.睾丸旁浆液性交界性肿瘤:7例报告
Am J Surg Pathol. 2001 Mar;25(3):373-8. doi: 10.1097/00000478-200103000-00012.
6
Malignant mesothelioma of the tunica vaginalis. A clinicopathologic analysis of 11 cases with review of the literature.睾丸鞘膜恶性间皮瘤。11例临床病理分析并文献复习
Am J Surg Pathol. 1995 Jul;19(7):815-25. doi: 10.1097/00000478-199507000-00010.
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Paratesticular serous papillary carcinoma. A report of six cases.
Am J Surg Pathol. 1995 Dec;19(12):1359-65. doi: 10.1097/00000478-199512000-00003.
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Serous papillary adenocarcinoma of the tunica vaginalis of the testis with metastasis.
Cancer. 1991 Mar 1;67(5):1450-3. doi: 10.1002/1097-0142(19910301)67:5<1450::aid-cncr2820670532>3.0.co;2-z.
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Serous papillary cystic tumor of borderline malignancy with focal carcinoma arising in testis: case report with immunohistochemical and ultrastructural observations.睾丸发生的伴局灶性癌的交界性浆液性乳头状囊性肿瘤:免疫组化和超微结构观察的病例报告
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睾丸转移性浆液性癌:一例报告并文献复习

Metastatic serous carcinoma of the testis: a case report and review of the literature.

作者信息

Ma Yuk Ting, Chaudhri Shalini, Cullen Michael H

机构信息

The Cancer Centre, University Hospital Birmingham NHS Foundation Trust, Birmingham, UK.

出版信息

Case Rep Oncol. 2011 Apr 18;4(1):246-9. doi: 10.1159/000327989.

DOI:10.1159/000327989
PMID:21589850
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3094581/
Abstract

Serous tumours of the testis and paratestis are rare, with fewer than 50 cases reported in the literature. The majority of the reported cases have been borderline serous tumours, and these tend not to recur or metastasize. Conversely, serous carcinomas can metastasize but this is often a late event. The presence of invasion in an otherwise borderline tumour has also been associated with the development of metastatic disease several years later, thus highlighting the importance of extensive sampling of all cases of borderline serous tumours. We report a case of a young man diagnosed with serous carcinoma of the testis, occurring 18 years after first diagnosis of a testicular germ cell tumour in the contralateral testis. This pattern has not previously been reported.

摘要

睾丸和睾丸旁的浆液性肿瘤很罕见,文献报道的病例不足50例。大多数报道的病例为交界性浆液性肿瘤,这些肿瘤往往不会复发或转移。相反,浆液性癌可发生转移,但这通常是晚期事件。在其他方面为交界性的肿瘤中出现浸润也与数年后转移性疾病的发生有关,因此凸显了对所有交界性浆液性肿瘤病例进行广泛取材的重要性。我们报告一例年轻男性病例,其在对侧睾丸首次诊断为睾丸生殖细胞肿瘤18年后被诊断为睾丸浆液性癌。这种情况此前未见报道。