Angina Bullosa Haemorrhagica (ABH) is a benign lesion of the oral cavity categorized by sudden onset of single or multiple blood filled lesions that burst leaving an ulcer that usually heals in 7-10 days without leaving a scar. We report a case of ABH diagnosed on the basis of history, clinical examination and blood, renal and liver function tests. The case findings and its management is discussed. Literature of the cases presented in the last 5 years was searched from Google Scholar and Pubmed. The review was summarized in a tabulated form.
Department of Clinical Epidemiology, Aarhus University and Aarhus University Hospital, Aarhus, Denmark; Department of Clinical Medicine, Aarhus University, Aarhus, Denmark; Department of Cardiology, Aarhus University Hospital, Aarhus, Denmark; Department of Cardiology, Gødstrup Regional Hospital, Herning, Denmark.
Background: Autoimmune blistering disorders (ABDs) might elevate cardiovascular risk, but studies are lacking.
Objective: The objective of this study was to examine if ABDs elevate the risk of atherosclerotic cardiovascular disease, heart failure, arrhythmia, venous thromboembolism, and cardiovascular death.
Methods: A population-based cohort of Danish patients with ABD (≥18 years of age) diagnosed during 1996-2021 (n = 3322) was compared with an age- and sex-matched comparison cohort from the general population (n = 33,195).
Knochentumor-Referenzzentrum und DÖSAK, Referenzregister am Institut für Medizinische Genetik und Pathologie, Universitätsspital Basel, Universität Basel, Schweiz.
Angina bullosa haemorrhagica (ABH) is a condition characterized by the recurrent formation of blood blisters in the mouth, first identified in 1967 by Badham.
These blisters occur due to mechanical trauma to the mucosal tissue.
The relationship between ABH and underlying health issues like hypertension, diabetes, or long-term corticosteroid use remains uncertain and unconfirmed.
Staphylococcal scalded skin syndrom is a bullous dermatosis induced by exfoliating staphylococcal exotoxins. Children are most often affected. We report the case of a 6-month-old infant who had angina in the few days before leading up to bullous erythroderma and whose skin biopsy showed characteristic appearance of staphylococcal scalded skin syndrom.
