Bayrak Demirel Ozge, Koc Cansu, Tercan Ummahan, Abali Saygin, Kardelen Asli Derya, Yildiz Melek, Poyrazoglu Sukran, Bas Firdevs, Darendeliler Feyza
Pediatric Endocrinology Unit, Istanbul Faculty of Medicine, Department of Pediatrics, Istanbul University, Istanbul, Turkey.
School of Medicine, Department of Pediatrics, Pediatric Endocrinology, Acibadem Mehmet Ali Aydinlar University, Istanbul, Turkey.
Horm Res Paediatr. 2024 Dec 24:1-5. doi: 10.1159/000543329.
Thyrotoxic hypokalemic periodic paralysis (THPP) is a rare but severe complication of hyperthyroidism characterized by acute muscle weakness. This study reports the first case of THPP in an adolescent with type 1 diabetes mellitus (T1DM) and Graves' disease, triggered by high-dose insulin, high carbohydrate intake, and strenuous exercise. It highlights the clinical presentation, management, and implications of THPP in this context.
A 17-year-old male patient with T1DM and Graves' disease presented to the emergency department with weakness in the extremities. The patient had engaged in strenuous exercise and high-dose rapid-acting insulin, and consumed a large amount of rice shortly before the onset of the symptoms. He exhibited hypertension and tachycardia, with diminished muscle strength and deep tendon reflexes with severe hypokalemia (1.6 mmol/L). Treatment with potassium and magnesium replacements was initiated. The patient's symptoms resolved within 5 h, and his neurological examination was normalized. Hypokalemia did not recur during follow-up. All symptoms improved rapidly with potassium replacement, β-blocker therapy, and antithyroid treatment.
This case represents the first documented instance of THPP in an adolescent with T1DM and Graves' disease. This entity should be included in the differential diagnosis of acute paralysis in patients with known thyrotoxicosis or those exhibiting symptoms such as tachycardia and hypertension. Insulin treatment in a hyperthyroid diabetic patient may increase the risk of THPP.
甲状腺毒症性低钾性周期性麻痹(THPP)是一种罕见但严重的甲状腺功能亢进并发症,其特征为急性肌无力。本研究报告了首例1型糖尿病(T1DM)合并格雷夫斯病的青少年发生THPP的病例,该病例由高剂量胰岛素、高碳水化合物摄入和剧烈运动引发。本文强调了在此背景下THPP的临床表现、治疗及意义。
一名患有T1DM和格雷夫斯病的17岁男性患者因四肢无力就诊于急诊科。该患者在症状发作前不久进行了剧烈运动并注射了高剂量速效胰岛素,还食用了大量米饭。他出现高血压和心动过速,伴有肌力减弱和腱反射减弱以及严重低钾血症(1.6 mmol/L)。开始进行补钾和补镁治疗。患者症状在5小时内缓解,神经系统检查恢复正常。随访期间低钾血症未复发。通过补钾、β受体阻滞剂治疗和抗甲状腺治疗,所有症状迅速改善。
该病例是首例记录在案的T1DM合并格雷夫斯病的青少年发生THPP的病例。在已知甲状腺毒症患者或出现心动过速和高血压等症状的患者的急性麻痹鉴别诊断中应考虑到这一病症。甲状腺功能亢进的糖尿病患者接受胰岛素治疗可能会增加发生THPP的风险。