A rare manifestation of hypothyroid myopathy: Hoffmann's syndrome

Citations

SCOPUS

14

초록

Hypothyroid myopathy is observed frequently and the resolution of the clinical manifestations of myopathy following thyroid hormone replacement is well known. However, a specific subtype of hypothyroid myopathy, Hoffmann's syndrome, characterized by increased muscular mass (pseudohypertrophy), proximal muscle weakness, muscle stiffness and cramps, is rarely reported. Herein, we describe a 34-year-old male who presented with proximal muscle weakness and non-pitting edema of the lower extremities. He initially visited the neurology department where he was suspected of having polymyositis. Additional laboratory evaluation revealed profound autoimmune hypothyroidism and elevated muscle enzymes including creatine kinase. The patient was started on levothyroxine treatment and, subsequently, clinical symptoms and biochemical parameters resolved with the treatment. The present case highlights that hypothyroidism should be considered in the differential diagnosis of musculoskeletal symptoms even in the absence of overt manifestations of hypothyroidism. To our knowledge, this is the first case reported in Korea. © 2015 Korean Endocrine Society.

키워드

Creatine kinase; Hypothyroidism; Muscular diseases
제목
A rare manifestation of hypothyroid myopathy: Hoffmann's syndrome
저자
Lee K.W.; Kim S.H.; Kim K.J.; Kim S.H.; Kim H.Y.; Kim B.-J.; Kim S.G.; Choi D.S.
DOI
10.3803/EnM.2015.30.4.626
발행일
2015-12
유형
Article
저널명
Endocrinology and Metabolism
권
30
호
4
페이지
626 ~ 630