Moyamoya Disease-like Cerebrovascular Stenotic Lesions Are an Important Phenotype of POEMS Syndrome-associated Vasculopathy
Author:
Affiliation:
1. Department of Medicine (Neurology and Rheumatology), Shinshu University School of Medicine, Japan
2. Center for Medical Genetics, Shinshu University Hospital, Japan
Publisher
Japanese Society of Internal Medicine
Subject
General Medicine,Internal Medicine
Link
https://www.jstage.jst.go.jp/article/internalmedicine/advpub/0/advpub_7701-21/_pdf
Reference18 articles.
1. 1. Dispenzieri A. POEMS Syndrome: 2019 Update on diagnosis, risk-stratification, and management. American journal of hematology 94: 812-827, 2019.
2. 2. Lesprit P, Authier FJ, Gherardi R, et al. Acute arterial obliteration: a new feature of the POEMS syndrome? Medicine 75: 226-232, 1996.
3. 3. Fu FW, Rao J, Zheng YY, Wang HL, Yang JG, Zheng GQ. Ischemic stroke in patients with POEMS syndrome: a case report and comprehensive analysis of literature. Oncotarget 8: 89406-89424, 2017.
4. 4. Yamaguchi I, Satomi J, Yamamoto N, et al. Coexistence of Quasi-moyamoya Disease and POEMS Syndrome in a Patient with Intracranial Hemorrhage: A Case Report and Literature Review. NMC case report journal 4: 5-9, 2017.
5. 5. Sekiguchi T, Ishibashi S, Sasame J, et al. Recurrent stroke due to quasi-moyamoya disease associated with POEMS syndrome: An autopsy case. Journal of the neurological sciences 412: 116738, 2020.
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