書誌事項
- タイトル別名
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- IgG4-related Mikulicz's Disease: A Report of 3 Cases
- IgG4 カンレン Mikuliczビョウ ノ 3 ショウレイ
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説明
Introduction: We report three cases of hyper-IgG4 disease with synchronous or asynchronous lymphocytic infiltration onset, IgG4 positive plasma cell infiltration, and fibril formation in multiple exocrine glands and extranodal organs. IgG4-related sialadenitis attracting recent attention has yet to be clarified as a clinical entity.<br>Case report: Case 1, a 61-year-old man, had a submandibular gland sample showing IgG4-positive plasma cell infiltration. Case 2, a 61-year-old man, was diagnosed with IgG4-related Mikulicz's disease confirmed by a sublingual gland sample. Case 3, a 57-year-old woman, had a diagnosis of IgG4-related Mikulicz's disease confirmed based on labial and sublingual gland samples. All reported oral dryness and bilateral submandibular swelling. Cases 1 and 2 recovered following Predonine administration tapered from 30 or 20 mg.<br>Discussion: IgG4-related Mikulicz's disease must be recognized as a clinical entity, together with its diagnostic criteria and treatment. Sublingual gland biopsy should be done to confirm its diagnosis following sublingual gland swelling.
収録刊行物
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- 日本耳鼻咽喉科学会会報
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日本耳鼻咽喉科学会会報 113 (10), 798-804, 2010
一般社団法人 日本耳鼻咽喉科学会
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詳細情報 詳細情報について
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- CRID
- 1390282679988161664
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- NII論文ID
- 10028256544
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- NII書誌ID
- AN00191551
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- COI
- 1:STN:280:DC%2BC3cbmtVSltQ%3D%3D
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- ISSN
- 18830854
- 00306622
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- NDL書誌ID
- 10880748
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- PubMed
- 21061567
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