Hypernatremic myopathy caused by a hypothalamic mixed germ cell tumor mimicking polymyositis
Journal
Clinical Rheumatology
Journal Volume
26
Journal Issue
9
Pages
1591-1594
Date Issued
2007
Author(s)
Abstract
Hypernatremic myopathy was rarely reported in the literature and its clinical features have never been well-described. We present a 22-year-old man who had adipsic hypernatremia manifested with progressive proximal muscle weakness and remarkably high creatine kinase level that has never been reported in the cases of hypernatremic myopathy. His initial presentations were similar to that of polymyositis without the evidence of central nervous system dysfunction and hypopituitarism. The serum level of sodium at the beginning of myopathy is the lowest known in the literature. All the clinical presentations in this patient resulted from a hypothalamic mixed germ cell tumor with sub-acute intra-tumoral hemorrhage. ? Clinical Rheumatology 2006.
SDGs
Other Subjects
creatine kinase; desmopressin; sodium; adipsia; adult; article; brain hernia; case report; central nervous system disease; creatine kinase blood level; dehydration; diabetes insipidus; excision; germ cell tumor; histopathology; human; human tissue; hypernatremia; hypopituitarism; hypothalamus tumor; inappropriate vasopressin secretion; leg edema; lethargy; limb weakness; male; memory disorder; mixed tumor; muscle weakness; myalgia; myopathy; nuclear magnetic resonance imaging; physical examination; polymyositis; polyuria; priority journal; sodium blood level; tumor bleeding; urine osmolality; urine volume; weight reduction; Adult; Diagnosis, Differential; Humans; Hypernatremia; Hypothalamic Neoplasms; Male; Muscular Diseases; Neoplasms, Germ Cell and Embryonal; Polymyositis
Type
journal article