Department of Endocrinology, Sher-i-Kashmir Institute of Medical Sciences, Srinagar, India.
Endocrinol Metab (Seoul). 2015 Dec;30(4):604-6. doi: 10.3803/EnM.2015.30.4.604. Epub 2015 Sep 10.
Allgrove (Triple A) syndrome is a rare autosomal recessive disorder characterized by cardinal features of adrenal insufficiency due to adrenocorticotropic hormone (ACTH) resistance, achalasia, and alacrimia. It is frequently associated with neurological manifestations like polyneuropathy. Since its first description by Allgrove in 1978, approximately 100 cases have been reported in the literature. Here we report an 18-year-old boy diagnosed as having Allgrove syndrome, with ACTH resistant adrenal insufficiency, achalasia, alacrimia, and severe motor polyneuropathy. Alacrimia was the earliest feature evident at the age of 8 years. He presented with achalasia and adrenal insufficiency at 12 and 18 years respectively and developed neurological symptoms in the form of severe muscle wasting at the age of 15 years. Patients with Allgrove syndrome usually manifest adrenal insufficiency and achalasia during first decade of life. Our patient manifested adrenal insufficiency and achalasia in the second decade and manifested neurological dysfunction before adrenal dysfunction.
Allgrove(三 A)综合征是一种罕见的常染色体隐性遗传病,其特征为促肾上腺皮质激素(ACTH)抵抗导致的肾上腺皮质功能不全、贲门失弛缓症和眼干。它常伴有神经表现,如多发性神经病。自 1978 年 Allgrove 首次描述以来,文献中已报道了大约 100 例。在这里,我们报告了一例 18 岁的男孩,被诊断为 Allgrove 综合征,表现为 ACTH 抵抗性肾上腺皮质功能不全、贲门失弛缓症、眼干和严重的运动性多发性神经病。眼干是 8 岁时最早出现的特征。他分别在 12 岁和 18 岁时出现贲门失弛缓和肾上腺皮质功能不全,并在 15 岁时出现严重肌肉萎缩的神经症状。Allgrove 综合征患者通常在生命的第一个十年表现出肾上腺皮质功能不全和贲门失弛缓症。我们的患者在第二个十年表现出肾上腺皮质功能不全和贲门失弛缓症,并在肾上腺功能不全之前表现出神经功能障碍。