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一例患有腹膜后畸胎瘤的克兰费尔特综合征患者。

A case of Klinefelter syndrome with retroperitoneal teratoma.

作者信息

Yong D, Lim J G, Choi J R, Park Q, Yang C H, Choi S H, Jeong H J, Song K S

机构信息

Department of Clinical Pathology, Yonsei University College of Medicine, Seoul, Korea.

出版信息

Yonsei Med J. 2000 Feb;41(1):136-9. doi: 10.3349/ymj.2000.41.1.136.

Abstract

Klinefelter syndrome (KS) is often associated with various neoplasms, especially germ cell tumors. Mediastinum is the most favored site of extragonadal germ cell tumors with KS, which is somewhat different from those without KS. The retroperitoneal germ cell tumor in KS is very rare. A five-month-old boy with an abdominal mass was found to have a retroperitoneal tumor. After surgical removal, he was diagnosed to have mature cystic teratoma. Cytogenetic study of his peripheral lymphocytes revealed that his karyotype was consistent with KS. This case suggests that patients with KS might be at risk of having germ cell tumors in sites other than mediastinum. It also suggests that all cases with these tumors should be screened for the presence of karyotypic abnormalities, and it might help to assess the exact correlation between germ cell tumors and KS, and to treat them accordingly.

摘要

克兰费尔特综合征(KS)常与各种肿瘤相关,尤其是生殖细胞肿瘤。纵隔是KS患者性腺外生殖细胞肿瘤最常发生的部位,这与非KS患者有所不同。KS患者的腹膜后生殖细胞肿瘤非常罕见。一名五个月大的腹部有肿块的男童被发现患有腹膜后肿瘤。手术切除后,他被诊断为成熟囊性畸胎瘤。对其外周淋巴细胞进行细胞遗传学研究发现,其核型与KS一致。该病例表明,KS患者可能有在纵隔以外部位发生生殖细胞肿瘤的风险。这也表明,所有患有这些肿瘤的病例都应筛查核型异常的存在,这可能有助于评估生殖细胞肿瘤与KS之间的确切关联,并据此进行治疗。

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