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一名患有先天性无鼻畸形女性患者的低促性腺激素性性腺功能减退症

Hypogonadotropic hypogonadism in a female patient with congenital arhinia.

作者信息

Hunter Janel Darcy, Davis Melissa Ann, Law Jennifer Rachel

出版信息

J Pediatr Endocrinol Metab. 2017 Jan 1;30(1):101-104. doi: 10.1515/jpem-2016-0082.

Abstract

The association of anosmia and congenital hypogonadotropic hypogonadism (CHH) is well described; however, congenital arhinia is a malformation associated with CHH that occurs much more rarely. There have been three reports of male patients with hypogonadism and congenital arhinia in the literature to date. We present the first case of arhinia associated with CHH in a female patient. A 14 years and 8 months female with congenital arhinia presented with delayed puberty. Physical examination and laboratory evaluation were consistent with hypogonadotropic hypogonadism. She had no other hormone deficiencies and brain magnetic resonance imaging demonstrated a normal pituitary gland. Abdominal ultrasound showed a prepubertal uterus and ovaries. She was subsequently started on sex steroid treatment to induce secondary sexual characteristics. This case demonstrates that abnormalities of nasal development may provide an early diagnostic clue to hypogonadotropic hypogonadism, particularly in female patients who would not manifest classic signs of CHH in infancy (micropenis and cryptorchidism). Early diagnosis of CHH and timely initiation of sex steroid therapy is important to prevent comorbidities related to pubertal delay.

摘要

嗅觉丧失与先天性低促性腺激素性性腺功能减退(CHH)之间的关联已有详尽描述;然而,先天性无鼻是一种与CHH相关的畸形,其发生更为罕见。迄今为止,文献中已有三例关于性腺功能减退合并先天性无鼻男性患者的报道。我们报告了首例女性患者先天性无鼻合并CHH的病例。一名14岁8个月患有先天性无鼻的女性患者出现青春期发育延迟。体格检查和实验室评估与低促性腺激素性性腺功能减退相符。她无其他激素缺乏,脑部磁共振成像显示垂体正常。腹部超声显示子宫和卵巢处于青春期前状态。随后她开始接受性类固醇治疗以诱导第二性征发育。该病例表明,鼻腔发育异常可能为低促性腺激素性性腺功能减退提供早期诊断线索,尤其是对于在婴儿期不会表现出CHH典型体征(小阴茎和隐睾症)的女性患者。CHH的早期诊断以及及时启动性类固醇治疗对于预防与青春期延迟相关的合并症很重要。

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