Co-development of pyogenic granuloma and capillary hemangioma on the alveolar ridge associated with a dental implant: a case report
Autor: | Bong-Wook Park, Jung-Hui Jang, Mun-Jeong Choi, June-Ho Byun, Young-Hoon Kang, Jong-Sil Lee, Young-Il Kim |
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Jazyk: | angličtina |
Předmět: |
Male
medicine.medical_specialty Pathology Dental implant medicine.medical_treatment Case Report Hemangioma medicine Alveolar ridge Alveolar Process Humans Hemangioma Capillary Granuloma Pyogenic Aged Dental Implants Antithrombotic therapy Medicine(all) Gingival Neoplasms Pyogenic granuloma business.industry Capillary hemangioma Anticoagulants General Medicine medicine.disease Magnetic Resonance Imaging Surgery Peripheral giant-cell granuloma Granuloma Gingival Diseases Implant Warfarin business |
Zdroj: | Journal of Medical Case Reports |
ISSN: | 1752-1947 |
DOI: | 10.1186/1752-1947-8-192 |
Popis: | Introduction The development of various benign oral mucosal lesions associated with dental implants, such as pyogenic granuloma or peripheral giant cell granuloma, has been rarely reported. However, the occurrence of vascular diseases, such as hemangioma, related to dental implants has not been explored in the literature. In this study, we report a case of co-development of pyogenic granuloma and capillary hemangioma on the alveolar ridge associated with a dental implant in a patient undergoing antithrombotic therapy. To the best of our knowledge, this is first case of hemangioma formation associated with a dental implant. Case presentation A 68-year-old Korean man was referred for intermittent bleeding and a dome-shaped overgrowing mass on his upper alveolar ridge. He underwent dental implantation 5 years ago, and was started on warfarin for cerebral infarction a year ago. He had experienced gum bleeding and gingival mass formation 6 months after warfarinization; then, his implant fixture was removed. However, his gingival mass has been gradually increasing. The gingival mass was surgically excised, and revealed the coexistence of pyogenic granuloma and capillary hemangioma in histological analysis of the specimen. The lesion has showed no recurrence for more than a year. Conclusions Regarding immunostaining features, the endothelial cell markers, CD34 and CD31, and the mesenchymal cell marker, vimentin, were strongly detected, but cell proliferation marker, Ki-67, was negatively expressed in the endothelial cells of the hemangioma portion. However, in the pyogenic granuloma portion, CD34 was almost negatively detected, whereas vimentin and Ki-67 were highly detected in the fibroblast-like tumor cells. According to these heterogeneous characteristics of the lesion, the patient was diagnosed with coexistence of pyogenic granuloma and capillary hemangioma associated with the dental implant on the attached gingiva. We recommend that patients with dental implants who have chronic peri-implantitis under antithrombotic therapy should be closely followed to ensure early detection of oral mucosal abnormalities. |
Databáze: | OpenAIRE |
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