دورية أكاديمية

Case of cortical superficial siderosis presenting with corticobasal syndrome.

التفاصيل البيبلوغرافية
العنوان: Case of cortical superficial siderosis presenting with corticobasal syndrome.
المؤلفون: Miyazawa, Naotaka, Hasegawa, Itsuki, Mino, Toshikazu, Takeda, Akitoshi, Hatsuta, Hiroyuki, Yoshizaki, Takahito, Takao, Masaki, Itoh, Yoshiaki
المصدر: Neurology & Clinical Neuroscience; Mar2022, Vol. 10 Issue 2, p95-97, 3p
مصطلحات موضوعية: CEREBRAL hemorrhage, PARIETAL lobe, MAGNETIC resonance imaging, CEREBRAL amyloid angiopathy, BRAIN stem, CEREBRAL cortex
مستخلص: A 70‐year‐old man presented with slow gait and a clumsy hand on the right side. Neurological examination revealed dystonia and ideomotor apraxia in the right hand. A mask‐like face, rigidity in the right arm, and shuffling gait were noticed. Treatment with L‐dopa had no effect. He was clinically diagnosed with corticobasal syndrome (CBS). Susceptibility‐weighted images of brain magnetic resonance imaging showed low‐intensity areas on the surface of the cerebral cortex, especially on the left parietal lobe, brain stem, and cerebellum, indicating superficial siderosis (SS). Neuropathological examination revealed diffuse hemosiderin deposition over the surface of the brain, including the left parietal lobe. Cerebellar hemorrhage with rupture to the subarachnoid space was noticed. Cortical SS should, therefore, be included in the differential diagnosis of CBS. [ABSTRACT FROM AUTHOR]
Copyright of Neurology & Clinical Neuroscience is the property of Wiley-Blackwell and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
قاعدة البيانات: Complementary Index
الوصف
تدمد:20494173
DOI:10.1111/ncn3.12572