Volume 4, Issue 4 (11-2015)                   aumj 2015, 4(4): 278-282 | Back to browse issues page


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Koopaie M, Rafiyan Koopaie N, Salehi K. A Case Report of Angina Bullosa Haemorrhagica (ABH) in Patient with Churg Strauss Syndrome. aumj 2015; 4 (4) :278-282
URL: http://aums.abzums.ac.ir/article-1-383-en.html
1- Assistant Professor, Department of Oral Medicine and Diagnostic Sciences, Tehran Dental School, Tehran University of Medical Sciences, Tehran, Iran , m-koopaie@tums.ac.ir
2- Assistant Professor, Department of Oral Medicine and Diagnostic Sciences, Alborz Dental School, Alborz University of Medical Sciences, Karaj, Iran
3- Alborz University of Medical Sciences, Karaj, Iran
Abstract:   (5453 Views)

Bullosa Haemorrhagica (ABH) is a rare oral blood blisters disorder. This recurrent disorder is restricted to oral mucosa and its difference with other oral vesiculobullos disorders is that blood vesicles are formed after minor trauma and in the absence of any blood dyscrasia, vesiculobullos disease and systemic disorder. This blood blisters are without pain, with color of dark red and full of bloods that rapidly enlarge and rapidly burst. The incidence of Angina Bullosa Haemorrhagica is unknown. Diagnosis of this disorder and differentiation from vesiculobullos disease like pemphigus and pemphiguid is important for patient's health. In this report we introduce a 55 years old woman with a 4­years history of oral blood blisters. These vesicles were in lateral border and ventral surface of tongue and on the ferenum. In medical history the patient had churg strauss syndrome and using inhalation corticosteroid for control of asthmatic attacks (An etiologic factor for appearing or aggravation of the disease).

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Type of Study: Case Report | Subject: Special
Received: 2016/02/07 | Accepted: 2016/02/07 | Published: 2016/02/07

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