Item type |
学術雑誌論文 / Journal Article(1) |
公開日 |
2019-12-17 |
タイトル |
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タイトル |
Chronic Recurrent Osteomyelitis with Systemic Juvenile Idiopathic Arthritis |
言語 |
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言語 |
eng |
キーワード |
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主題Scheme |
Other |
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主題 |
autoinflammatory diseases |
キーワード |
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主題Scheme |
Other |
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主題 |
chronic recurrent multiple osteomyelitis |
キーワード |
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主題Scheme |
Other |
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主題 |
arthritis |
キーワード |
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主題Scheme |
Other |
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主題 |
interleukin-6 |
キーワード |
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主題Scheme |
Other |
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主題 |
tumor necrosis factor-alpha |
資源タイプ |
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資源タイプ識別子 |
http://purl.org/coar/resource_type/c_6501 |
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資源タイプ |
journal article |
著者 |
Arakawa, Naoya
Takizawa, Takumi
Nishida, Yutaka
Yagi, Hisao
Arakawa, Hirokazu
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抄録 |
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内容記述タイプ |
Abstract |
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内容記述 |
A 14-year-old-boy presented with pain and a lump on his left lower leg.Magnetic resonance imaging (MRI)revealed a medullary lesions on T1-weighted images and medullary enhancement after contrast injection. Bone marrow biopsy with curettage revealed an active marrow without evidence of malignancy or infection. The patient had acne on his face and legs. Accordingly, he was diagnosed with chronic recurrent multiple osteomyelitis (CRMO)syndrome. A few months later, the patient developed shoulder joint pain, remittent fever, and an erythematous rash accompanied by a high fever. Blood tests revealed elevated levels of CRP (10.2 mg╱dL) and ferritin (557 ng╱mL), and hypoalbuminemia (2.8 g╱dL).A second bone marrow biopsy revealed hemophagocytosis, but no malignancies. Subsequently,a diagnosis of systemic juvenile idiopathic arthritis (s-JIA) was established. |
書誌情報 |
The Kitakanto medical journal = 北関東医学
巻 68,
号 3,
p. 167-169,
発行日 2018-08-01
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ISSN |
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収録物識別子タイプ |
ISSN |
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収録物識別子 |
1343-2826 |
書誌レコードID |
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収録物識別子タイプ |
NCID |
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収録物識別子 |
AN10585677 |
著者版フラグ |
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出版タイプ |
VoR |
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出版タイプResource |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
出版者 |
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出版者 |
北関東医学会 |
資源タイプ |
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内容記述タイプ |
Other |
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内容記述 |
Journal Article |
更新日 |
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日付 |
2019-12-18 |
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日付タイプ |
Created |