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ID 67722
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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
Abstract
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.
Published Date
2024-10-28
Publication Title
Case Reports in Dentistry
Volume
volume2024
Publisher
Wiley
Start Page
8836103
ISSN
2090-6447
Content Type
Journal Article
language
English
OAI-PMH Set
岡山大学
Copyright Holders
© 2024 Hideka Kanemoto et al.
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publisher
PubMed ID
DOI
Web of Science KeyUT
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isVersionOf https://doi.org/10.1155/2024/8836103
License
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