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ANGINA BULLOSA HEMORRHAGICA OF THE ORAL CAVITY: A 14-YEAR RETROSPECTIVE STUDY IN A BRAZILIAN POPULATION

To report the clinical features of angina bullosa hemorrhagica (ABH) cases, emphasizing the clinical and therapeutic characteristics. A retrospective descriptive cross‐sectional study was performed in 3 oral and maxillofacial pathology services and 1 private practice in Brazil. Clinical data were co...

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Bibliographic Details
Published in:Oral surgery, oral medicine, oral pathology and oral radiology oral medicine, oral pathology and oral radiology, 2022-09, Vol.134 (3), p.e193-e193
Main Authors: Cavalcante, Israel Leal, Cunha, John Lennon Silva, Da Silva Barros, Caio César, Felix, Fernanda Aragão, Da Silveira, Éricka Janine Dantas, De Andrade, Bruno Augusto Benevenuto, De Sousa, Sílvia Ferreira
Format: Article
Language:English
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Summary:To report the clinical features of angina bullosa hemorrhagica (ABH) cases, emphasizing the clinical and therapeutic characteristics. A retrospective descriptive cross‐sectional study was performed in 3 oral and maxillofacial pathology services and 1 private practice in Brazil. Clinical data were collected from the clinical records and evaluated. The series comprised 12 males (52.2%) and 11 females (47.8%), with a mean age of 56.8 ± 14.6 years. Most of the lesions affected the soft palate (n = 15, 65.2%) and tongue (n = 6, 26.1%). Clinically, the lesions presented mainly as an asymptomatic (n = 17, 73.9%) blood-filled blister that ruptured after a few minutes or hours, leaving an erosion. When specified, the masticatory trauma was the most frequent triggering event. No individual had coagulation disorders. Treatment was symptomatic with a favorable outcome. ABH is still poorly documented in the literature, and its etiology remains uncertain. ABH mainly affects the soft palate of elderly adults and has a favorable evolution in a few days. However, it can share some clinical features with more serious diseases. Therefore, a careful clinical examination is essential to rule out possible autoimmune or hematologic disorders.
ISSN:2212-4403
2212-4411
DOI:10.1016/j.oooo.2022.01.588