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Seminoma in a male phenotype 46XX true hermaphrodite.

机译:男性表型中的精原细胞为真XXH雌雄同体。

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摘要

Although true hermaphrodite is uncommon, it has been reported in more than 400 individuals. Tumours arising in the gonads of true hermaphrodite is a very rare finding and only very few cases have been reported in the literature. We report a case of a 35-year-old phenotype man with bilateral undescended testis with lump hypogastrium. On examination, he had an ovotestis on one side and pure seminoma arising in testis on the other side. The seminoma arising in the left undescended testis was successfully treated by excision and combination chemotherapy. Cytogenetic studies revealed that 46XX karyotype with primer specific for the sex-determining region of the Y chromosome was negative. The karyotypic abnormality noticed in the patient is also reviewed in the article.
机译:尽管真正的雌雄同体并不常见,但已有400多个人报告。真正的雌雄同体性腺中产生的肿瘤是非常罕见的发现,文献中只有极少数的病例报道。我们报告一例35岁的表型男子与双侧睾丸不全伴有胃下垂肿大。经检查,他的一侧有卵睾丸,另一侧有睾丸产生的精原细胞瘤。通过切除和联合化疗成功治疗了左侧睾丸中的精原细胞瘤。细胞遗传学研究表明,带有特异性针对Y染色体性别决定区域的引物的46XX核型为阴性。文章中还回顾了患者中发现的核型异常。

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