青春期发育不全时耻骨过早——文献综述和两例病例报告。

Anna Rakuś-Kwiatosz, Elżbieta Budzyńska, Iwona Beń-Skowronek
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引用次数: 0

摘要

引言:婴儿期孤立性耻骨过早(PP)可能是许多诊断困难的原因。这是由于发病率低,因此,对该主题的研究数量有限,并且由于促性腺激素和雄激素浓度在小青春期的生理变异性,缺乏严格的实验室标准。材料和方法:我们旨在根据文献综述和2例青春期发育不全的男性婴儿阴囊毛,介绍目前对婴儿期PP的了解。结果:男孩在青春期早期的阴部孤立毛发需要鉴别诊断。在排除了严重的病因后,它似乎是性早熟的一种温和的、自我限制的变体。这种现象可能是毛囊对短暂增加的雄激素浓度的敏感性增加的结果。结论:婴儿期孤立性阴毛是婴儿性早熟的一种轻度、自限性变体,应作为排除诊断。这种情况会自行缓解,但绝对需要进一步随访,以排除青春期进展的严重病因。
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Premature pubarche during minipuberty - literature review and two case reports.

Introduction: Isolated premature pubarche (PP) in infancy may be the reason for many diagnostic difficulties. This is due to the low incidence and, therefore, the limited number of studies on this subject and the lack of strict laboratory standards because of the physiological variability of gonadotropic hormone and androgen concentrations during minipuberty.

Material and methods: We aimed to present current knowledge about PP in infancy based on the literature review and 2 cases of male infants with scrotal hair during minipuberty.

Results: Isolated hair in the pubic region in a boy during the period of minipuberty requires differential diagnosis. After excluding serious aetiology, it seems to be a mild, self-limiting variant of precocious puberty. The phenomenon is probably a result of increased sensitivity of the hair follicles to transiently increased androgen concentration.

Conclusions: Isolated pubic hair in infancy as a mild, self-limiting variant of precocious puberty in infants should be a diagnosis of exclusion. The condition resolves spontaneously, but it absolutely requires further follow-up to exclude serious aetiology in the case of puberty progression.

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来源期刊
Pediatric Endocrinology, Diabetes and Metabolism
Pediatric Endocrinology, Diabetes and Metabolism Medicine-Pediatrics, Perinatology and Child Health
CiteScore
2.00
自引率
0.00%
发文量
36
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