Cargando…

A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes

We present a case of a 58-year-old man with delayed diagnosed moyamoya disease who underwent encephaloduroarteriosynangiosis (EDAS) procedure. This patient with a history of three strokes presented to our facility with new left facial droop. Neurological examination revealed left facial droop and he...

Descripción completa

Detalles Bibliográficos
Autores principales: Mohammadi, Oranus, Krieger, David, Butt, Ifrah, Danckers, Mauricio
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975246/
https://www.ncbi.nlm.nih.gov/pubmed/32010532
http://dx.doi.org/10.7759/cureus.6446
_version_ 1783490256802152448
author Mohammadi, Oranus
Krieger, David
Butt, Ifrah
Danckers, Mauricio
author_facet Mohammadi, Oranus
Krieger, David
Butt, Ifrah
Danckers, Mauricio
author_sort Mohammadi, Oranus
collection PubMed
description We present a case of a 58-year-old man with delayed diagnosed moyamoya disease who underwent encephaloduroarteriosynangiosis (EDAS) procedure. This patient with a history of three strokes presented to our facility with new left facial droop. Neurological examination revealed left facial droop and hemiparesis. Brain magnetic resonance imaging (MRI) described right frontal lobe acute ischemia. Head computed tomography (CT) angiography revealed bilateral supraclinoid internal carotid artery (ICA) occlusions. Cerebral angiography demonstrated diffuse intracranial vascular irregularity with stenosis, more above the bilateral supraclinoid ICAs and the right middle cerebral artery (MCA) suggestive of moyamoya disease. Due to the lack of MCA patency, he underwent EDAS. Superficial temporal artery (STA) was dissected inferiorly and the posterior branch was bipolared, then STA was movable. A bur hole made at the superior and inferior portion along the STA. Dura was opened, and STA was brought on top of the pia. His facial droop gradually improved after that. Nine months later, no new strokes reported. Moyamoya disease is a rare neurovascular disorder characterized by narrowing and occlusion of the ICA branches. Its symptoms include recurrent ischemic/hemorrhagic strokes. Incidence in Hispanics has not been studied. The gap between the first manifestations and disease progression is one to eight years. Its diagnosis is often delayed. Our patient had recurrent strokes for five years. Despite therapy with antiplatelets, new ischemic stroke brought him to our institution. Rate of recurrent strokes despite antiplatelets was reported 10.3% per year. Brain CTs and MRIs had failed to detect strokes’ etiology. Catheter-directed angiography is the gold standard test for diagnosis of moyamoya disease. Antiplatelet alone is ineffective and surgery is the effective method to prevent further strokes, although there are no studies in adults regarding the efficacy of indirect revascularization. In direct revascularization, usually STA anastomoses to MCA. Indirect method works through the development of leptomeningeal collaterals. Postoperative complications are infarction and hyperperfusion syndrome. Seong-eun et al. proposed that modified EDAS is simpler with less complications in comparison with direct revascularization. Some other studies showed higher chance of stroke in indirect method versus direct technique. In conclusion, it is important to consider moyamoya disease as a differential diagnosis in patients with recurrent strokes.
format Online
Article
Text
id pubmed-6975246
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher Cureus
record_format MEDLINE/PubMed
spelling pubmed-69752462020-01-31 A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes Mohammadi, Oranus Krieger, David Butt, Ifrah Danckers, Mauricio Cureus Neurosurgery We present a case of a 58-year-old man with delayed diagnosed moyamoya disease who underwent encephaloduroarteriosynangiosis (EDAS) procedure. This patient with a history of three strokes presented to our facility with new left facial droop. Neurological examination revealed left facial droop and hemiparesis. Brain magnetic resonance imaging (MRI) described right frontal lobe acute ischemia. Head computed tomography (CT) angiography revealed bilateral supraclinoid internal carotid artery (ICA) occlusions. Cerebral angiography demonstrated diffuse intracranial vascular irregularity with stenosis, more above the bilateral supraclinoid ICAs and the right middle cerebral artery (MCA) suggestive of moyamoya disease. Due to the lack of MCA patency, he underwent EDAS. Superficial temporal artery (STA) was dissected inferiorly and the posterior branch was bipolared, then STA was movable. A bur hole made at the superior and inferior portion along the STA. Dura was opened, and STA was brought on top of the pia. His facial droop gradually improved after that. Nine months later, no new strokes reported. Moyamoya disease is a rare neurovascular disorder characterized by narrowing and occlusion of the ICA branches. Its symptoms include recurrent ischemic/hemorrhagic strokes. Incidence in Hispanics has not been studied. The gap between the first manifestations and disease progression is one to eight years. Its diagnosis is often delayed. Our patient had recurrent strokes for five years. Despite therapy with antiplatelets, new ischemic stroke brought him to our institution. Rate of recurrent strokes despite antiplatelets was reported 10.3% per year. Brain CTs and MRIs had failed to detect strokes’ etiology. Catheter-directed angiography is the gold standard test for diagnosis of moyamoya disease. Antiplatelet alone is ineffective and surgery is the effective method to prevent further strokes, although there are no studies in adults regarding the efficacy of indirect revascularization. In direct revascularization, usually STA anastomoses to MCA. Indirect method works through the development of leptomeningeal collaterals. Postoperative complications are infarction and hyperperfusion syndrome. Seong-eun et al. proposed that modified EDAS is simpler with less complications in comparison with direct revascularization. Some other studies showed higher chance of stroke in indirect method versus direct technique. In conclusion, it is important to consider moyamoya disease as a differential diagnosis in patients with recurrent strokes. Cureus 2019-12-22 /pmc/articles/PMC6975246/ /pubmed/32010532 http://dx.doi.org/10.7759/cureus.6446 Text en Copyright © 2019, Mohammadi et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Neurosurgery
Mohammadi, Oranus
Krieger, David
Butt, Ifrah
Danckers, Mauricio
A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title_full A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title_fullStr A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title_full_unstemmed A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title_short A Case of Delayed Diagnosis of Moyamoya Disease After Recurrent Strokes
title_sort case of delayed diagnosis of moyamoya disease after recurrent strokes
topic Neurosurgery
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6975246/
https://www.ncbi.nlm.nih.gov/pubmed/32010532
http://dx.doi.org/10.7759/cureus.6446
work_keys_str_mv AT mohammadioranus acaseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT kriegerdavid acaseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT buttifrah acaseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT danckersmauricio acaseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT mohammadioranus caseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT kriegerdavid caseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT buttifrah caseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes
AT danckersmauricio caseofdelayeddiagnosisofmoyamoyadiseaseafterrecurrentstrokes