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ID 67722
フルテキストURL
fulltext.pdf 1.53 MB
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 researchmap
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 researchmap
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 researchmap
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.
発行日
2024-10-28
出版物タイトル
Case Reports in Dentistry
2024巻
出版者
Wiley
開始ページ
8836103
ISSN
2090-6447
資料タイプ
学術雑誌論文
言語
英語
OAI-PMH Set
岡山大学
著作権者
© 2024 Hideka Kanemoto et al.
論文のバージョン
publisher
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1155/2024/8836103
ライセンス
https://creativecommons.org/licenses/by/4.0/
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