Literature DB >> 16581493

Moyamoya disease associated with Behcet's disease.

Sung Pil Joo1, Tae Sun Kim, Je Hyuk Lee, Jung Kil Lee, Jae Hyoo Kim, Soo Han Kim, Myeong Kyu Kim, Ki-Hyun Cho.   

Abstract

A 32-year-old woman with Behcet's disease suffered repeated transient ischemic attacks (TIA) consisting of left hemiparesis. Cerebral angiography revealed the typical findings of moyamoya disease, with occlusion of the supraclinoid portion of both internal carotid arteries, coupled with abnormal collateral vessels. She underwent right superficial temporal artery to middle cerebral artery (STA-MCA) anastomosis and encephalomyosynangiosis, due to decreased reserve capacity demonstrated on acetazolamide single positron emission computed tomography (SPECT). Postoperatively, the TIA symptoms subsided. This is the first report of moyamoya disease associated with Behcet's disease, and moyamoya disease should be considered in the differential diagnosis of cerebrovascular events in patients with Behcet's disease. Revascularization surgery is recommended for the prevention of ischemic insults resulting in permanent deficits.

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Year:  2006        PMID: 16581493     DOI: 10.1016/j.jocn.2005.03.040

Source DB:  PubMed          Journal:  J Clin Neurosci        ISSN: 0967-5868            Impact factor:   1.961


  1 in total

1.  Moyamoya syndrome occurred in a girl with an inactive systemic lupus erythematosus.

Authors:  Yun-Jin Lee; Gyu Min Yeon; Sang Ook Nam; Su Yung Kim
Journal:  Korean J Pediatr       Date:  2013-12-20
  1 in total

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