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  1. Public
  2. 研究紀要
  3. ACTA MEDICA KINDAI UNIVERSITY
  4. 43(2)2018

<Case Reports> A rare case of a severe ocular complication as an initial presentation of adolescent-onset systemic lupus erythematosus: a case report

https://kindai.repo.nii.ac.jp/records/20126
https://kindai.repo.nii.ac.jp/records/20126
13865060-cb04-4be9-87a8-7a20bb444d49
名前 / ファイル ライセンス アクション
AA0050842X-20181200-0081.pdf AA0050842X-20181200-0081.pdf (1.0 MB)
Item type ☆紀要論文 / Departmental Bulletin Paper(1)
公開日 2019-06-17
タイトル
タイトル <Case Reports> A rare case of a severe ocular complication as an initial presentation of adolescent-onset systemic lupus erythematosus: a case report
言語 en
著者 Kotani, Yuki

× Kotani, Yuki

Kotani, Yuki

ja-Kana コタニ, ユキ

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Miyazaki, Kohei

× Miyazaki, Kohei

Miyazaki, Kohei

ja-Kana ミヤザキ, コウヘイ

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Enya, Takuji

× Enya, Takuji

Enya, Takuji

ja-Kana エンヤ, タクジ

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Miyazawa, Tomoki

× Miyazawa, Tomoki

Miyazawa, Tomoki

ja-Kana ミヤザワ, トモキ

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Okada, Mitsuru

× Okada, Mitsuru

Okada, Mitsuru

ja-Kana オカダ, ミツル

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Sugimoto, Keisuke

× Sugimoto, Keisuke

Sugimoto, Keisuke

ja-Kana スギモト, ケイスケ

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言語
言語 eng
キーワード
主題 children systemic, lupus erythematosus, retinopathy
資源タイプ
資源タイプ識別子 http://purl.org/coar/resource_type/c_6501
資源タイプ departmental bulletin paper
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
著者 所属
値 Department of Pediatrics, Kindai University Faculty of Medicine
版
出版タイプ NA
出版タイプResource http://purl.org/coar/version/c_be7fb7dd8ff6fe43
出版者 名前
出版者 Kindai University Medical Association
書誌情報 en : ACTA MEDICA KINDAI UNIVERSITY

巻 43, 号 2, p. 81-88, 発行日 2018-12
ISSN
収録物識別子タイプ ISSN
収録物識別子 03866092
抄録
内容記述タイプ Abstract
内容記述 [Abstract] Background: Systemic lupus erythematosus (SLE) is an autoimmune disease that causes severe complications in multiple organs. Ocular manifestations are critical in patients with SLE because of the vision-threatening risk of such complications. However, severe retinopathy as an initial presentation of SLE is uncommon, even when the severity of SLE is mild, especially in children. Case presentation: We encountered a 14-year-old female patient with rapidly progressive impairment of her left vision that was determined to be caused by severe retinopathy secondary to SLE. Her other systemic symptoms, including a mild renal disorder, were not severe. The patient showed positivity for anticardiolipin antibody, although she did not have antiphospholipid antibody syndrome. She was initially treated with high-dose methylprednisolone, antiplatelet therapy,and anticoagulation therapy because of the high possibility of vision loss; this was followed by tacrolimus as maintenance therapy. Photocoagulation therapy was also performed to prevent vitreous hemorrhage and retinal detachment. Early diagnosis of SLE based on the rapid deterioration of her vision allowed for early interventions and a good clinical course with recovery of her vision. Conclusions: Importantly, regardless of the severity of the systemic symptoms in patients with SLE, ocular involvement is critical and requires aggressive treatment.
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内容記述 application/pdf
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