Two pediatric cases of reversible cerebral vasoconstriction syndrome due to cortical subarachnoid hemorrhaging
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- Nonaka Futaba
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
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- Haraguchi Kohei
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
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- Sato Tatsuharu
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
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- Miyazaki Akane
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
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- Watanabe Asami
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
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- Moriuchi Hiroyuki
- Department of Pediatrics, Nagasaki University Hospital, Nagasaki
Bibliographic Information
- Other Title
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- 皮質性くも膜下出血により可逆性脳血管れん縮症候群の診断に至った小児の2例
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Abstract
<p> Reversible cerebral vasoconstriction syndrome (RCVS) is characterized by thunderclap headache onset and multifocal segmental cerebral vasoconstriction. This syndrome is seen predominantly in women between 20 and 50 years old. Although its prognosis is good, there are various complications of RCVS, including intracerebral hemorrhaging, subarachnoid hemorrhaging (SAH), and posterior reversible encephalopathy syndrome. Previously healthy 7- and 12-year-old boys developed cortical SAH after a thunderclap headache. Cranial computed tomography angiography and cranial magnetic resonance angiography indicated multifocal segmental cerebral vasoconstriction. RCVS was diagnosed from the clinical course and these neuroimaging findings. One was treated with calcium channel blockers, and neither had neurological sequelae. RCVS should be considered in the differential diagnosis of pediatric patients complaining of thunderclap headaches or developing cortical SAH. It is important to perform neuroimaging studies serially for these patients.</p>
Journal
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- NO TO HATTATSU
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NO TO HATTATSU 56 (1), 53-57, 2024
The Japanese Society of Child Neurology
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Keywords
Details 詳細情報について
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- CRID
- 1390298986213219072
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- ISSN
- 18847668
- 00290831
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- Text Lang
- ja
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- Data Source
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- JaLC
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- Abstract License Flag
- Disallowed