Case of Moyamoya Disease Aggravated during the Treatment of Behçet’s Disease.
10.4078/jrd.2016.23.6.386
- Author:
Eun Seong PARK
1
;
Yoon Jeong OH
;
Byung Woo YOO
;
Sung Soo AHN
;
Jin Su PARK
;
Pyeong Ho YOON
;
Chan Hee LEE
Author Information
1. Department of Internal Medicine, Yonsei University College of Medicine, Seoul, Korea.
- Publication Type:Case Report
- Keywords:
Behcet syndrom;
Intestinal Behçet’s disease;
Moyamoya disease;
Aggravated
- MeSH:
Adult;
Carotid Artery, Internal;
Cerebral Arteries;
Cerebrovascular Disorders;
Constriction, Pathologic;
Diarrhea;
Female;
Fever;
Hand;
Hemorrhage;
Humans;
Moyamoya Disease*;
Oral Ulcer;
Steroids;
Vasculitis
- From:Journal of Rheumatic Diseases
2016;23(6):386-391
- CountryRepublic of Korea
- Language:English
-
Abstract:
Behçet’s disease (BD) is a multi-organ involved inflammatory disorder described by recurrent oral ulcers and other systemic manifestations. Almost all the clinical manifestations of BD are believed to be due to vasculitis. On the other hand, the cerebral arteries are rarely involved. Moyamoya disease (MMD) is an unusual chronic cerebrovascular disorder that is described by bilateral progressive stenosis or occlusion of the internal carotid artery and an abnormal collateral vascular network. A 32-year-old woman with MMD was referred for fever, oral pain, and diarrhea, and was diagnosed with BD. Her MMD was aggravated during treatment with high dose steroids to control the intestinal BD and a reduction in the MMD medication due to gastrointestinal bleeding. This is the first reported case of intestinal BD in a patient previously diagnosed with MMD, who experienced aggravation of her MMD after the cessation of MMD medication due to aggravated intestinal BD.
