Dyke-Davidoff-Masson syndrome-like picture in a case of Takayasu arteritis: an enigma. (11th September 2012)

• Record Type: Journal Article
• Authors: Roy, Krishnendu; Talukdar, Arunansu; Ray, Sayantan; Pal, Partha
• Is Part Of: BMJ case reports. Volume 2012
• Publication Date: 2012-09-11
• Subjects: Medicine -- Case studies -- Periodicals; 610.5
• DOI: 10.1136/bcr-2012-006669
• Languages: English
• ISSNs: 1757-790X

Abstract

Abstract : Authors describe the case of a 16-year-old girl who presented with fever, tonic–clonic seizures, unequal arm blood pressures and pulselessness in the left upper limb. On examination, there was a systolic bruit over umbilical region, a pansystolic murmur of mitral regurgitation was found. Neurological examination was normal except for an asymmetry in brain hemicircumference one side compared with the other. She has borderline intelligence (IQ 70) according to Wechsler Adult Performance Intelligence Scale. Magnetic resonance imaging (MRI) of brain revealed atrophic of left cerebral hemisphere with mildly ventricular dilatation, prominent paranasal and mastoid air cells, suggestive of Dyke-Davidoff-Masson syndrome (DDMS). Conventional angiography showed narrowed left internal carotid artery. There was also stenosed brachial artery, absent left renal artery with narrowed infrarenal abdominal aorta. The patient was put on antihypertensive drugs. We hypothesise that Takayasu arteritis and related vascular occlusion is the cause of her acquired cerebral changes.