Aynaou Hayat, Salhi Houda, El Ouahabi Hanan
Department of Endocrinology, Diabetology, Metabolic Diseases and Nutrition, Hassan II University Hospital, Fez, MAR.
Cureus. 2022 May 5;14(5):e24752. doi: 10.7759/cureus.24752. eCollection 2022 May.
A 30-year-old woman presented with a 15-day history of epigastric pain, nausea, vomiting, asthenia, and weight loss. On admission, hypercalcemia was reported with a negative etiologic workup (including no primary hyperparathyroidism, malignancy, or vitamin D toxicity). Fluid replacement did not improve her hypercalcemia. We performed a blood ionogram and assessed the adrenocortical function, which showed that her serum cortisol was decreased, her adrenocorticotropic hormone (ACTH) was elevated, and anti-21 hydroxylase antibodies were positive. We established the diagnosis of autoimmune primary acute adrenal insufficiency. The patient was treated with hydrocortisone. Shortly after initiating the treatment, her serum calcium levels returned to normal and her symptoms improved. This case report highlights the fact that even though adrenal insufficiency is an uncommon etiology of hypercalcemia, it should not be totally ignored, especially since hypercalcemia can sometimes be indicative of adrenal impairment.
一名30岁女性,有15天的上腹部疼痛、恶心、呕吐、乏力和体重减轻病史。入院时报告有高钙血症,病因检查结果为阴性(包括无原发性甲状旁腺功能亢进、恶性肿瘤或维生素D中毒)。补液治疗未能改善她的高钙血症。我们进行了血液离子分析并评估了肾上腺皮质功能,结果显示她的血清皮质醇降低,促肾上腺皮质激素(ACTH)升高,抗21羟化酶抗体呈阳性。我们确诊为自身免疫性原发性急性肾上腺功能不全。该患者接受了氢化可的松治疗。开始治疗后不久,她的血清钙水平恢复正常,症状也有所改善。本病例报告强调了这样一个事实,即尽管肾上腺功能不全是高钙血症的罕见病因,但不应完全被忽视,特别是因为高钙血症有时可能提示肾上腺功能受损。