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Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report
Progressive moyamoya disease in pregnancy and puerperium has not been reported previously. Here, we present a 39-year-old woman who had been found to have moderate stenosis of right middle cerebral artery (MCA) 4 years prior to her pregnancy, finally suffering minor completed stroke due to progressi...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The Japan Neurosurgical Society
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533379/ https://www.ncbi.nlm.nih.gov/pubmed/25263620 http://dx.doi.org/10.2176/nmc.cr.2014-0071 |
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author | AKAMATSU, Yosuke FUJIMURA, Miki UENOHARA, Hiroshi SHIMIZU, Hiroaki TOMINAGA, Teiji |
author_facet | AKAMATSU, Yosuke FUJIMURA, Miki UENOHARA, Hiroshi SHIMIZU, Hiroaki TOMINAGA, Teiji |
author_sort | AKAMATSU, Yosuke |
collection | PubMed |
description | Progressive moyamoya disease in pregnancy and puerperium has not been reported previously. Here, we present a 39-year-old woman who had been found to have moderate stenosis of right middle cerebral artery (MCA) 4 years prior to her pregnancy, finally suffering minor completed stroke due to progressive moyamoya disease at the early postpartum period. Three days after cesarean section without any complication, she developed cerebral infraction at right hemisphere, when magnetic resonance angiography indicated apparent progression of the proximal MCA stenosis. Catheter angiography demonstrated nearly occlusion of the right terminal internal carotid artery (ICA) and the development of an abnormal vascular network at the base of the brain as well as MCA stenosis, indicating a definitive diagnosis of moyamoya disease with unilateral involvement. The patient underwent superficial temporal artery-middle cerebral artery anastomosis 1 month after the onset of stroke, and she did not manifest as further neurological events during the follow-up period of 2 years. Moyamoya disease could newly develop in pregnancy and puerperium, which should be noted as a pitfall of the management of moyamoya disease with pregnancy. |
format | Online Article Text |
id | pubmed-4533379 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | The Japan Neurosurgical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-45333792015-11-05 Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report AKAMATSU, Yosuke FUJIMURA, Miki UENOHARA, Hiroshi SHIMIZU, Hiroaki TOMINAGA, Teiji Neurol Med Chir (Tokyo) Case Report Progressive moyamoya disease in pregnancy and puerperium has not been reported previously. Here, we present a 39-year-old woman who had been found to have moderate stenosis of right middle cerebral artery (MCA) 4 years prior to her pregnancy, finally suffering minor completed stroke due to progressive moyamoya disease at the early postpartum period. Three days after cesarean section without any complication, she developed cerebral infraction at right hemisphere, when magnetic resonance angiography indicated apparent progression of the proximal MCA stenosis. Catheter angiography demonstrated nearly occlusion of the right terminal internal carotid artery (ICA) and the development of an abnormal vascular network at the base of the brain as well as MCA stenosis, indicating a definitive diagnosis of moyamoya disease with unilateral involvement. The patient underwent superficial temporal artery-middle cerebral artery anastomosis 1 month after the onset of stroke, and she did not manifest as further neurological events during the follow-up period of 2 years. Moyamoya disease could newly develop in pregnancy and puerperium, which should be noted as a pitfall of the management of moyamoya disease with pregnancy. The Japan Neurosurgical Society 2014-10 2014-09-29 /pmc/articles/PMC4533379/ /pubmed/25263620 http://dx.doi.org/10.2176/nmc.cr.2014-0071 Text en © 2014 The Japan Neurosurgical Society This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. To view a copy of this license, visit http://creativecommons.org/licenses/by-nc-nd/4.0/ |
spellingShingle | Case Report AKAMATSU, Yosuke FUJIMURA, Miki UENOHARA, Hiroshi SHIMIZU, Hiroaki TOMINAGA, Teiji Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title | Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title_full | Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title_fullStr | Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title_full_unstemmed | Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title_short | Development of Moyamoya Disease in Pregnancy and Puerperium: Case Report |
title_sort | development of moyamoya disease in pregnancy and puerperium: case report |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4533379/ https://www.ncbi.nlm.nih.gov/pubmed/25263620 http://dx.doi.org/10.2176/nmc.cr.2014-0071 |
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