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CASE REPORT
Year : 2019  |  Volume : 33  |  Issue : 1  |  Page : 56-58

Angina bullosa hemorrhagica: A rare case report in known asthmatic on inhaled corticosteroids


1 Department of Respiratory Medicine, NKP Salve Institute of Medical Sciences and RC, Nagpur, Maharashtra, India
2 Department of Dermato- Venereo- Leprology, Government Medical College and Hospital, Nagpur, Maharashtra, India
3 Department of Pharmacology, Government Medical College and Hospital, Nagpur, Maharashtra, India

Correspondence Address:
Dr. Bhagyashree Babanrao Supekar
C/O Supekar Niwas, Behind Shinde Hospital, D. P. Road, Adarsh Nagar, Beed - 431 122, Maharashtra
India
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijaai.ijaai_24_18

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Angina bullosa hemorrhagica (ABH) is characterized by development of acute onset of painless solitary or multiple blood-filled vesicles or bullae in oral mucosa which are not attributed to blood dyscrasias, vesiculobullous disorder, and systemic diseases. These lesions rupture spontaneously to form ragged, often painless, superficial erosions that heal spontaneously within 1 week without scarring. Trauma appears to be the most common identifiable precipitating factor. We report a case of ABH to emphasize the importance of recognition of this relatively rare benign condition and to differentiate it from other dermatological and systemic causes of oral blisters.


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