Severe Alveolar Bone Loss as a Rare Manifestation of Suspected Intestinal Behçet Disease: A Case Report

Oral ulcers commonly occur in Behçet disease, but severe alveolar bone loss is rarely documented. We report a case where marked periodontal destruction preceded the diagnosis of suspected intestinal Behçet disease. A 21-year-old man presented with extensive palatal ulcers and severe maxillary alveolar bone loss extending to the root apices. Radiographic examination revealed localized bone destruction confined to the palatal region. Subsequent evaluation revealed intestinal lesions characteristic of Behçet disease. A combination of systemic medications (prednisolone, mesalazine, and infliximab) and periodontal care stabilized both oral and intestinal conditions. This case highlights that severe alveolar bone destruction can manifest as a complication of intestinal Behçet disease, underscoring the importance of thorough oral examinations and integrated medical-dental care.

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Publication Details

Journal
Mayo Clinic Proceedings Innovations Quality & Outcomes
Published
2025-04-16
DOI
https://doi.org/10.1016/j.mayocpiqo.2025.100612
Citations
1
Primary Topic
Ocular Diseases and Behçet’s Syndrome
Type
article
Field-Weighted Citation Impact
1.71
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article

Severe Alveolar Bone Loss as a Rare Manifestation of Suspected Intestinal Behçet Disease: A Case Report

Satoshi Usuda, Satoru Morikawa, Taneaki Nakagawa, Takanori Kanai∥ et al.
1 citations
Mayo Clinic Proceedings Innovations Quality & Outcomes
Ocular Diseases and Behçet’s Syndrome
1.71
article

Severe Alveolar Bone Loss as a Rare Manifestation of Suspected Intestinal Behçet Disease: A Case Report

Satoshi Usuda, Satoru Morikawa, Taneaki Nakagawa, Takanori Kanai∥, Kazuyuki Tsunoda, Yuta Kaieda
article en
1 citations

Abstract

Oral ulcers commonly occur in Behçet disease, but severe alveolar bone loss is rarely documented. We report a case where marked periodontal destruction preceded the diagnosis of suspected intestinal Behçet disease. A 21-year-old man presented with extensive palatal ulcers and severe maxillary alveolar bone loss extending to the root apices. Radiographic examination revealed localized bone destruction confined to the palatal region. Subsequent evaluation revealed intestinal lesions characteristic of Behçet disease. A combination of systemic medications (prednisolone, mesalazine, and infliximab) and periodontal care stabilized both oral and intestinal conditions. This case highlights that severe alveolar bone destruction can manifest as a complication of intestinal Behçet disease, underscoring the importance of thorough oral examinations and integrated medical-dental care.

Mayo Clinic Proceedings Innovations Quality & OutcomesVol. 9(3)
Keio University (JP)
Zero hunger
Openalex Percentile: Top 20%
Ocular Diseases and Behçet’s Syndrome
1.71
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