ID | 67722 |
フルテキストURL | |
著者 |
Kanemoto, Hideka
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Obata, Kyoichi
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kadoya, Koichi
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Ono, Kisho
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kaken ID
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Kawai, Hotaka
Department of Oral Pathology and Medicine, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
Kunisada, Yuki
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
ORCID
Kaken ID
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Yao, Mayumi
Department of Oral and Maxillofacial Surgery, Tsuyama Chuo Hospital
Ibaragi, Soichiro
Department of Oral and Maxillofacial Surgery, Okayama University Graduate School of Medicine, Dentistry and Pharmaceutical Sciences
ORCID
Kaken ID
publons
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抄録 | Amyloidosis is a disease in which amyloid protein is deposited in organs and tissues, resulting in functional impairment. Amyloidosis occurs in 12%-30% of patients with multiple myeloma, but in rare cases, amyloidosis may precede the diagnosis of multiple myeloma. Our patient was a 76-year-old Japanese male on dialysis. Multiple nodules accompanied by ulcers were observed on his tongue. He had no subjective symptoms or clinical findings associated with multiple myeloma. The histopathological findings suggested amyloidosis. We suspected both systemic and localized amyloidosis and performed a comprehensive systemic examination. Since the patient had been on dialysis for only a short period of time (similar to 3 months), dialysis-related amyloidosis was ruled out. After blood and urine tests, a diagnosis of multiple myeloma was made. Chemotherapy treatment was started, but the patient's multiple myeloma could not be suppressed and the tongue amyloidosis worsened, leading to his death 2 years and 2 months after the initial diagnosis.
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発行日 | 2024-10-28
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出版物タイトル |
Case Reports in Dentistry
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巻 | 2024巻
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出版者 | Wiley
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開始ページ | 8836103
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ISSN | 2090-6447
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資料タイプ |
学術雑誌論文
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言語 |
英語
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OAI-PMH Set |
岡山大学
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著作権者 | © 2024 Hideka Kanemoto et al.
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論文のバージョン | publisher
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DOI | |
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関連URL | isVersionOf https://doi.org/10.1155/2024/8836103
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ライセンス | https://creativecommons.org/licenses/by/4.0/
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Citation | Kanemoto, Hideka, Obata, Kyoichi, Kadoya, Koichi, Ono, Kisho, Kawai, Hotaka, Kunisada, Yuki, Yao, Mayumi, Ibaragi, Soichiro, A Rare Case of Multiple Myeloma Identified Following the Diagnosis of Amyloidosis of the Tongue, Case Reports in Dentistry, 2024, 8836103, 5 pages, 2024. https://doi.org/10.1155/2024/8836103
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