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Angina Bullosa Hemorrhagica: Report of Two Cases

Angina bullosa hemorrhagic (ABH) describes the acute and sometimes painful onset of oral blood-filled vesicles and bullae, not attributable to blood dyscrasia, vesiculobullous disorders, systemic diseases or other known causes. The haemorrhagic bullae spontaneously burst after a short time resulting...

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Detalles Bibliográficos
Autores principales: Rai, Shalu, Kaur, Mandeep, Goel, Sumit
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519269/
https://www.ncbi.nlm.nih.gov/pubmed/23248380
http://dx.doi.org/10.4103/0019-5154.103083
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author Rai, Shalu
Kaur, Mandeep
Goel, Sumit
author_facet Rai, Shalu
Kaur, Mandeep
Goel, Sumit
author_sort Rai, Shalu
collection PubMed
description Angina bullosa hemorrhagic (ABH) describes the acute and sometimes painful onset of oral blood-filled vesicles and bullae, not attributable to blood dyscrasia, vesiculobullous disorders, systemic diseases or other known causes. The haemorrhagic bullae spontaneously burst after a short time resulting in ragged, often painless, superficial erosions that heal spontaneously within 1 week without scarring. Trauma appears to be the most common identifiable precipitating factor, but the essential tissue defect is yet unidentified. This paper presents two cases of ABH with the aim to create awareness regarding occurrence of this lesion, thus avoiding any misdiagnosis.
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spelling pubmed-35192692012-12-17 Angina Bullosa Hemorrhagica: Report of Two Cases Rai, Shalu Kaur, Mandeep Goel, Sumit Indian J Dermatol E–Case Report Angina bullosa hemorrhagic (ABH) describes the acute and sometimes painful onset of oral blood-filled vesicles and bullae, not attributable to blood dyscrasia, vesiculobullous disorders, systemic diseases or other known causes. The haemorrhagic bullae spontaneously burst after a short time resulting in ragged, often painless, superficial erosions that heal spontaneously within 1 week without scarring. Trauma appears to be the most common identifiable precipitating factor, but the essential tissue defect is yet unidentified. This paper presents two cases of ABH with the aim to create awareness regarding occurrence of this lesion, thus avoiding any misdiagnosis. Medknow Publications & Media Pvt Ltd 2012 /pmc/articles/PMC3519269/ /pubmed/23248380 http://dx.doi.org/10.4103/0019-5154.103083 Text en Copyright: © Indian Journal of Dermatology http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open-access article distributed under the terms of the Creative Commons Attribution-Noncommercial-Share Alike 3.0 Unported, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle E–Case Report
Rai, Shalu
Kaur, Mandeep
Goel, Sumit
Angina Bullosa Hemorrhagica: Report of Two Cases
title Angina Bullosa Hemorrhagica: Report of Two Cases
title_full Angina Bullosa Hemorrhagica: Report of Two Cases
title_fullStr Angina Bullosa Hemorrhagica: Report of Two Cases
title_full_unstemmed Angina Bullosa Hemorrhagica: Report of Two Cases
title_short Angina Bullosa Hemorrhagica: Report of Two Cases
title_sort angina bullosa hemorrhagica: report of two cases
topic E–Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3519269/
https://www.ncbi.nlm.nih.gov/pubmed/23248380
http://dx.doi.org/10.4103/0019-5154.103083
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