Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy

A 36-year-old man visited our hospital because of blurred vision and redness of the conjunctiva. Slit-lamp examination showed panuveitis. Two days later, he suddenly experienced dizziness, speech disturbance, paralysis of his right extremities, and gait disturbances. Neurological examinations sugges...

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Main Authors: Natsuyo Yoshida-Hata, Shigeko Yashiro, Noritoshi Arai, Sousuke Takeuchi
Format: Article
Language:English
Published: Hindawi Limited 2012-01-01
Series:Case Reports in Medicine
Online Access:http://dx.doi.org/10.1155/2012/356743
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spelling doaj-966e906950a94a19ad0b2e676364ba1c2020-11-24T20:58:02ZengHindawi LimitedCase Reports in Medicine1687-96271687-96352012-01-01201210.1155/2012/356743356743Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse TherapyNatsuyo Yoshida-Hata0Shigeko Yashiro1Noritoshi Arai2Sousuke Takeuchi3Department of Ophthalmology, National Center for Global Health and Medicine, Tokyo 162-8655, JapanDepartment of Ophthalmology, National Center for Global Health and Medicine, Tokyo 162-8655, JapanDepartment of Neurology, National Center for Global Health and Medicine, Tokyo 162-8655, JapanDepartment of Neurology, National Center for Global Health and Medicine, Tokyo 162-8655, JapanA 36-year-old man visited our hospital because of blurred vision and redness of the conjunctiva. Slit-lamp examination showed panuveitis. Two days later, he suddenly experienced dizziness, speech disturbance, paralysis of his right extremities, and gait disturbances. Neurological examinations suggested that his symptoms were caused by a left lateral medullary lesion. He also had erythema mainly on his trunk. Magnetic resonance imaging (MRI) of his brain demonstrated a small infarct on the left side of the medulla oblongata. Clinical presentation and MRI findings were consistent with the diagnosis of a Wallenberg’s syndrome. He also had bilateral hilar lymphadenopathy. A skin biopsy showed granulomatous nodular dermatitis compatible with sarcoidosis. He was treated with steroid pulse therapy and his neurological and ocular symptoms immediately improved. Only seven similar cases of intracranical sarcoidosis have been reported, but none had been treated with steroid pulse therapy. We recommend that steroid pulse therapy be considered to treat patients with sarcoidosis with signs of lesions in the central nervous system.http://dx.doi.org/10.1155/2012/356743
collection DOAJ
language English
format Article
sources DOAJ
author Natsuyo Yoshida-Hata
Shigeko Yashiro
Noritoshi Arai
Sousuke Takeuchi
spellingShingle Natsuyo Yoshida-Hata
Shigeko Yashiro
Noritoshi Arai
Sousuke Takeuchi
Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
Case Reports in Medicine
author_facet Natsuyo Yoshida-Hata
Shigeko Yashiro
Noritoshi Arai
Sousuke Takeuchi
author_sort Natsuyo Yoshida-Hata
title Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
title_short Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
title_full Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
title_fullStr Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
title_full_unstemmed Brainstem Infarction and Panuveitis due to Sarcoidosis Successfully Treated with Steroid Pulse Therapy
title_sort brainstem infarction and panuveitis due to sarcoidosis successfully treated with steroid pulse therapy
publisher Hindawi Limited
series Case Reports in Medicine
issn 1687-9627
1687-9635
publishDate 2012-01-01
description A 36-year-old man visited our hospital because of blurred vision and redness of the conjunctiva. Slit-lamp examination showed panuveitis. Two days later, he suddenly experienced dizziness, speech disturbance, paralysis of his right extremities, and gait disturbances. Neurological examinations suggested that his symptoms were caused by a left lateral medullary lesion. He also had erythema mainly on his trunk. Magnetic resonance imaging (MRI) of his brain demonstrated a small infarct on the left side of the medulla oblongata. Clinical presentation and MRI findings were consistent with the diagnosis of a Wallenberg’s syndrome. He also had bilateral hilar lymphadenopathy. A skin biopsy showed granulomatous nodular dermatitis compatible with sarcoidosis. He was treated with steroid pulse therapy and his neurological and ocular symptoms immediately improved. Only seven similar cases of intracranical sarcoidosis have been reported, but none had been treated with steroid pulse therapy. We recommend that steroid pulse therapy be considered to treat patients with sarcoidosis with signs of lesions in the central nervous system.
url http://dx.doi.org/10.1155/2012/356743
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