a child with moyamoya disease: case report
نویسندگان
چکیده
cerebral stroke is a rare disease in children. moyamoya (mm) is one of the infrequent cerebrovascular diseases with unknown etiology. we report an 8 year-old-boy with chief complain of sudden onset bilateral parietal lobe headache. he mentioned that his headache was first started about three weeks ago and was associated with visual disturbance. his mother declared that the boy developed gait problems few days later and only could walk with assistance. he was diagnosed with mm disease. after, medical treatment his symptoms were mildly improved and because of his family disagreement cerebral revascularization surgery was not performed.
منابع مشابه
Long-term Outcome of Motor Function in a Child with Moyamoya Disease: A Case Report
[Purpose] This observational study provides a retrospective description of changes in motor function of a 10 year old child who suffered from motor weakness caused by Moyamoya disease (MMD) over an approximately 3 year follow-up observation period. [Methods] The child was diagnosed as MMD due to multifocal encephalomalacia in both frontal and parietal cortices. After the ischemic attack, the ch...
متن کاملMoyamoya disease associated with ankylosing spondylitis in a 9-year-old child: a case report
Background: Ankylosing spondylitis was reported to associate with an increased risk of cerebrovascular diseases. In this article, we aimed to report the first case of ankylosing spondylitis associated with moyamoya disease treated with encephalo-duroarterio-synangiosis. Case presentation: A 9-year-old boy with ankylosing spondylitis appeared a symptom of repeated transient ischemic attacks whic...
متن کاملExtravasation from anterior choroidal artery in a child with moyamoya disease--case report.
A rare association of moyamoya disease with intra- and periventricular hemorrhage in an 8-year-old girl is presented. Angiography showed that the cause of hemorrhage was extravasation from the dilated anterior choroidal artery. Ventriculoperitoneal shunt and encephalomyosynangiosis have prevented clinical or neurological deficits for over 6 years.
متن کاملMoyamoya disease in a patient with brain tumor: case report.
A 40-year-old male presented to emergency room with epileptic grand mal seizure. He had untreated hypertension, and prior diagnostic investigation showed duplex renal arteries of the right kidney with hyperreninemia in the left renal vein. He was nonsmoker, with moderate alcohol intake. Neurologic examination was normal except for high blood pressure and tongue bite. Electroencephalogram was no...
متن کاملMoyamoya disease with posterior communicating artery aneurysm: a case report.
In moyamoya disease (MMD), subsequent aneurysm in the proximal part of the posterior communicating artery (PcomA) is extremely rare. We report the case of a middle-aged female patient with MMD, who presented with a ruptured wide-necked aneurysm at the proximal part of the developed PcomA that converged with the posterior cerebral artery (PCA) and supplied the distal area. Endovascular treatment...
متن کاملHematologic manifestations in a child with HIV a Case Report
Abstract Background Immune deficiency in human might be primary or secondary and could be seen with a wide variety of manifestations. In the following, we presented a Child with various complains that diagnosed to have HIV infection. Case Report A 2/5 y/o child was admitted to the hospital for FUO with prolonged cough, FTT, cervical lymphadenopathy, hepatosplenomegaly and bilateral opti...
متن کاملمنابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
international clinical neurosciences journalجلد ۲، شماره ۲، صفحات ۷۴-۷۶
میزبانی شده توسط پلتفرم ابری doprax.com
copyright © 2015-2023