Neuropediatrics 1998; 29(5): 265-267
DOI: 10.1055/s-2007-973572
Short communications

© Hippokrates Verlag GmbH Stuttgart

Hypertension in Leigh Syndrome -A Case Report

T. Narita1 , T. Yamano1 , M. Ohno1 , T. Takano1 , R. Ito2 , M. Shimada1
  • 1Departments of Pediatrics, Shiga University of Medical Science, Seta, Otsushi, Shiga-ken, 520-21, Japan
  • 2Departments of Radiology, Shiga University of Medical Science, Seta, Otsushi, Shiga-ken, 520-21, Japan
Further Information

Publication History

Publication Date:
12 March 2007 (online)

Abstract

A female patient, who was diagnosed with Leigh syndrome at 15 months of age, developed fulminating severe hypertension and died at 8 years of age. Hypertension has not been reported as an important clinical symptom in Leigh syndrome. Laboratory findings indicated that it was not associated with endocrinopathic diseases such as pheochromocytoma and aldosteronism, or renal diseases. Brain MRI scan showed symmetrical lesions in the basal ganglia and medulla oblongata including the nucleus tractus solitarius.

This nucleus is known to play an important role in maintaining blood pressure. Since the medulla oblongata is a vulnerable site, potential development of hypertension should be taken into consideration when managing Leigh syndrome.