Université Paris Descartes, Sorbonne Paris Cité, and Assistance Publique-Hôpitaux de Paris, Hôpital Bicêtre, Unité d'Endocrinologie Pédiatrique, Le Kremlin Bicêtre, France.
PLoS One. 2011;6(10):e26516. doi: 10.1371/journal.pone.0026516. Epub 2011 Oct 18.
Congenital isolated adrenocorticotrophic hormone (ACTH) deficiency may be rare, but it could be an underestimated cause of neonatal death. Our objective was to shorten the time between first symptoms and diagnosis.
This single-centre retrospective case-cohort study was carried out on eight consecutive patients.
Two had the neonatal form and 6 the late onset form. Six were admitted to an intensive care unit at least once for seizures with hypoglycemia, major hypothermia, fever, and/or collapsus. The 2 neonatal cases presented with hypoglycemia and in a state of "apparent death" at birth or hypothermia (29°C) at 6 days. All 6 late onset cases had also been admitted to an emergency department 1-3 times, but had left hospital incorrectly diagnosed. Their first symptoms were noted at 3-12.3 years, and they were diagnosed at 3.3-14.4 years. All had hypoglycemia, and 4 had had seizures. The presenting symptoms were vomiting and/or abdominal pain, asthenia, irritability, difficulty with physical activities, and anorexia. The school performance of 4 deteriorated. Two underwent psychotherapy and treatment for depression, which was stopped when Hydrocortisone® replacement therapy began. The plasma concentrations in spontaneous hypoglycemia were: ACTH<5 to 17.1 pg/mL, with concomitant cortisol <3.5 to 37 ng/mL. The plasma dehydroepiandrosterone sulfate (DHAS) concentrations were low in the 7 evaluated. The coding sequence of TPIT was normal in all.
Several unexplained symptoms in a child, mainly gastro-intestinal symptoms and seizures due to hypoglycemia, may indicate ACTH deficiency. A low or normal basal plasma ACTH despite concomitant low cortisol at 8 a.m. and/or in spontaneous hypoglycemia, associated with low DHAS, in a patient not given corticosteroids is highly suggestive of ACTH deficiency. The isolated character of ACTH deficiency must be confirmed by determining the other hypothalamic-pituitary functions, and Hydrocortisone® replacement therapy initiated in emergency.
先天性孤立性促肾上腺皮质激素(ACTH)缺乏症可能很少见,但它可能是新生儿死亡被低估的原因。我们的目的是缩短从首次出现症状到确诊的时间。
这是一项在 8 名连续患者中进行的单中心回顾性病例对照研究。
2 例为新生儿型,6 例为晚发型。6 例因低血糖性癫痫、严重低体温、发热和/或虚脱至少一次入住重症监护病房。2 例新生儿病例在出生时表现为低血糖和“明显死亡”状态,或在 6 天时体温为 29°C。所有 6 例晚发型病例也曾因症状在 1-3 次到急诊就诊,但均被误诊出院。他们的首发症状为 3-12.3 岁,确诊时为 3.3-14.4 岁。所有患者均有低血糖,4 例有癫痫发作。首发症状为呕吐和/或腹痛、乏力、易激惹、体力活动困难和食欲不振。4 例的学习成绩下降。2 例接受了心理治疗和抑郁症治疗,当开始使用 Hydrocortisone®替代疗法时停止了治疗。自发性低血糖时的血浆浓度为:ACTH<5 至 17.1 pg/mL,同时皮质醇<3.5 至 37 ng/mL。7 例中评估的脱氢表雄酮硫酸酯(DHAS)浓度均较低。所有患者的 TPIT 编码序列均正常。
儿童出现的一些不明原因的症状,主要是胃肠道症状和低血糖性癫痫,可能提示 ACTH 缺乏。在未使用皮质激素的情况下,即使在上午 8 点和/或自发性低血糖时同时存在低皮质醇,而基础血浆 ACTH 水平低或正常,同时 DHAS 水平低,高度提示 ACTH 缺乏。必须通过确定其他下丘脑-垂体功能来确认孤立性 ACTH 缺乏症的特征,并在紧急情况下开始 Hydrocortisone®替代治疗。