首页> 外文期刊>International Journal of Clinical and Experimental Pathology >Pseudomembranous trigonitis in a male with Klinefelter syndrome: a case report and evidence of a hormonal etiology
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Pseudomembranous trigonitis in a male with Klinefelter syndrome: a case report and evidence of a hormonal etiology

机译:男性克氏综合征的伪膜性三角炎:一例病例报告和激素病因学证据

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Klinefelter syndrome is a clinical syndrome with a distinct 47, XXY karyotype. Patients are characterized by a tall eunuchoid stature, small testes, hypergonotrophic hypogonadism, gynecomastia, learning difficulties and infertility. These patients have also been found to have raised estrogen levels. We report a 16 year old boy with Klinefelter syndrome presenting to our institution with gross hematuria. Cystoscopy and biopsy revealed the diagnosis of pseudomembranous trigonitis. Immunohistochemical stains showed an increase in estrogen and progesterone receptors in the trigone area but not in the rest of the bladder. In view of the patient’s mildly raised estrogen levels and the histological findings, we postulate that estrogen is the driver of the development of pseudomembranous trigonitis. This is the first reported case of pseudomembranous trigonitis seen in association with Klinefelter syndrome, and also the first case of pseudomembranous trigonitis occurring within the male adolescent age group.
机译:Klinefelter综合征是具有独特的47个XXY核型的临床综合征。患者的特征是高的太监体形,小睾丸,高食神经性性腺功能低下,男性乳房发育,学习困难和不育。还发现这些患者的雌激素水平升高。我们向我们的机构报告了一名16岁的克氏综合征男孩,他患有严重的血尿。膀胱镜检查和活检显示为假膜性三角炎的诊断。免疫组织化学染色显示在三角区中雌激素和孕激素受体增加,但在膀胱其余部分则没有。考虑到患者的雌激素水平轻度升高和组织学发现,我们推测雌激素是假膜性三角炎发展的驱动力。这是首次报告的与Klinefelter综合征相关的假膜性三角炎病例,也是在男性青少年年龄段发生的第一例假膜性三角炎病例。

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