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当神经性厌食症的症状掩盖了卡尔曼综合征。

When anorexia nervosa symptoms mask Kallmann syndrome.

机构信息

Child Psychiatry Department, Hôpital Erasme-Université libre de Bruxelles, Route de Lennik 808, 1070, Brussels, Belgium.

出版信息

Eat Weight Disord. 2022 Jun;27(5):1903-1906. doi: 10.1007/s40519-021-01332-z. Epub 2021 Dec 2.

Abstract

BACKGROUND

Although anorexia nervosa might delay puberty, a structured assessment at its onset remains crucial in excluding congenital delayed puberty diseases.

CASE PRESENTATION

During the follow-up of a 15-year-old girl suffering from anorexia nervosa, a change of treatment has led to a thorough medical history revealing the absence of the olfactory bulb. Kallmann syndrome diagnosis was made on a blood analysis and the patient was treated with a multidisciplinary approach.

CONCLUSION

After the diagnosis, our patient was relieved as it has clarified some of her symptoms including anosmia, poor height and maturational delay. Too often a delayed puberty is attributed to anorexia nervosa itself without considering medical history. This case definitely shows the importance of performing a case history and early diagnosis in pre-pubertal AN to rule out other rare diseases and avoid mid- and long-term sequelae.

LEVEL OF EVIDENCE

IV (case study).

摘要

背景

尽管神经性厌食症可能会延迟青春期,但在发病时进行结构化评估仍然至关重要,以排除先天性青春期延迟疾病。

病例介绍

在对一名患有神经性厌食症的 15 岁女孩进行随访时,治疗方案的改变导致了详细的病史回顾,发现其嗅球缺失。通过血液分析诊断为卡尔曼综合征,患者接受了多学科治疗。

结论

诊断后,我们的患者感到如释重负,因为这解释了她的一些症状,包括嗅觉丧失、身高矮小和发育迟缓。青春期延迟往往归因于神经性厌食症本身,而不考虑病史。这个病例明确表明,在青春期前神经性厌食症中进行病史采集和早期诊断非常重要,以排除其他罕见疾病并避免中期和长期的后遗症。

证据水平

IV(病例研究)。

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