| Literature DB >> 28101185 |
Chuifen Wu1, Jun Xin2, Minghua Xin2, Hai Zou3, Lie Jing3, Caoyong Zhu3, Wenhui Lei3.
Abstract
Primary aldosteronism (PA) is a rare disorder. The majority of patients with PA present with typical features and are easily diagnosed. This disorder is usually diagnosed with hypokalemia, hypertension or an adrenal mass. However, patients with atypical symptoms may present a challenge for diagnosis and treatment. In the present study, a case of PA is described that presented with hypokalemic myopathy simulating polymyositis. The patient was a 44-year-old woman who presented with weakness and difficulty walking. The patient was initially suspected to have PM and was treated with methylprednisolone. The patient was found to have hypokalemia which persisted despite high-dose supplementation of potassium. Adrenal computed tomography revealed a right adrenal mass. Surgical adrenalectomy was conducted. The final pathological diagnosis was benign adrenocortical adenoma. The serum tests remained normal and the patient's symptoms were resolved during the 8-month follow-up.Entities:
Keywords: hypokalemic myopathy; primary aldosteronism
Year: 2016 PMID: 28101185 PMCID: PMC5228118 DOI: 10.3892/etm.2016.3864
Source DB: PubMed Journal: Exp Ther Med ISSN: 1792-0981 Impact factor: 2.447