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在不孕不育检查中发现极高的抗苗勒氏管激素水平,提示存在伴有环状小管的性索肿瘤和潜在的 Peutz-Jeghers 综合征:病例报告。

Extremely high anti-Mullerian hormone levels detected during infertility workup revealing sex cord tumor with annular tubules and underlying Peutz-Jeghers syndrome: A case report.

机构信息

Department of Obstetrics and Gynecology, Assisted Reproductive Technologies Clinic, Kocaeli University, Faculty of Medicine, Kocaeli, Turkey.

Department of Obstetrics and Gynecology, Division of Gynecologic Oncology, Kocaeli University, Faculty of Medicine, Kocaeli, Turkey.

出版信息

J Obstet Gynaecol Res. 2022 Feb;48(2):492-496. doi: 10.1111/jog.15107. Epub 2021 Nov 27.

Abstract

We report an infertile, but otherwise asymptomatic woman, whose extremely high anti-Mullerian hormone (AMH) level detected during infertility investigation led to the diagnosis of sex cord tumor with annular tubules (SCTAT) which is a very rare sex cord-stromal tumor (SCST) and eventually revealed a previously undiagnosed hereditary cancer syndrome, Peutz-Jeghers syndrome (PJS). A 33-year-old woman attended Kocaeli University ART Clinic for infertility evaluation. Her AMH level was 319.63 ng/ml. Detection of bilateral ovarian cysts required surgical evaluation. The histopathological examination of ovaries revealed SCTAT. The strong association of SCTAT with PJS raised the suspicion of this syndrome. Whole STK11 gene sequencing confirmed PJS diagnosis. AMH has become a widely used tool in the evaluation of infertile women. Clinicians dealing with infertility should be familiar with the utility of AMH measurement besides being a marker of ovarian reserve. Detection of high AMH concentrations should raise the suspicion of an SCST.

摘要

我们报告了一例不孕但无症状的女性,她在不孕症检查中发现极高的抗苗勒管激素(AMH)水平,导致诊断为性索-管状腺肿瘤(SCTAT),这是一种非常罕见的性索-间质肿瘤(SCST),最终揭示了先前未诊断的遗传性癌症综合征——Peutz-Jeghers 综合征(PJS)。一名 33 岁女性因不孕到科贾埃利大学 ART 诊所就诊。她的 AMH 水平为 319.63ng/ml。双侧卵巢囊肿的发现需要手术评估。卵巢的组织病理学检查显示 SCTAT。SCTAT 与 PJS 的强烈关联引起了对该综合征的怀疑。STK11 全基因测序证实了 PJS 的诊断。AMH 已成为评估不孕女性的常用工具。除了作为卵巢储备的标志物外,处理不孕症的临床医生还应熟悉 AMH 测量的用途。检测到高 AMH 浓度应引起对 SCST 的怀疑。

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