Indian Journal of Allergy Asthma and Immunology (Jan 2019)

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

  • Sonal Suresh Arsude,
  • Bhagyashree Babanrao Supekar,
  • Ankita Sunilrao Jire

DOI
https://doi.org/10.4103/ijaai.ijaai_24_18
Journal volume & issue
Vol. 33, no. 1
pp. 56 – 58

Abstract

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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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