Proulx F, Weber M L, Collu R, Lelièvre M, Larbrisseau A, Delisle M
Department of Paediatrics, Hôpital Sainte-Justine, Université de Montréal, Québec, Canada.
Eur J Pediatr. 1993 Jun;152(6):526-9. doi: 10.1007/BF01955066.
We report the case of a 9-year-old girl with multiple problems due to hypothalamic dysfunction of obscure origin: apnoeic spells, behavioural problems, developmental delay, hypodipsia with bouts of hypernatraemia, episodes of spontaneous hypothermia, obesity, petit-mal seizures, non-progressive precocious puberty, absence of respiratory response to CO2 and probably insensitivity of hyposensitivity to pain. She also had hyperprolactinaemia and decreased human growth hormone secretion. Hypothyroidism of central origin and hyposecretion of cortisol were also present. Multiple brain CT-scans failed to reveal any tumour or other anatomical abnormality. Her clinical course was improved initially by treatment with clomipramine, but she died suddenly, and the autopsy failed to disclose any anatomical lesion. We compare this case with three similar previously reported cases.
我们报告了一名9岁女孩的病例,该女孩因不明原因的下丘脑功能障碍出现多种问题:呼吸暂停发作、行为问题、发育迟缓、低渴感伴高钠血症发作、自发性体温过低发作、肥胖、失神发作、非进行性性早熟、对二氧化碳无呼吸反应以及可能对疼痛低敏或不敏感。她还患有高催乳素血症和生长激素分泌减少。同时存在中枢性甲状腺功能减退和皮质醇分泌减少。多次脑部CT扫描未发现任何肿瘤或其他解剖学异常。最初使用氯米帕明治疗后她的临床病程有所改善,但她突然死亡,尸检未发现任何解剖学病变。我们将此病例与之前报道的三个类似病例进行了比较。