Pregled bibliografske jedinice broj: 399561
IgA mediated pemphigus precipitated by glibenclamide – a case report
IgA mediated pemphigus precipitated by glibenclamide – a case report // Abstract of the 9th biennial Congress of the European Association of Oral Medicine / Baum, Bruce ; Scully, Crispian (ur.).
Salzburg: Wiley-Blackwell, 2008. str. 36-36 (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 399561 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
IgA mediated pemphigus precipitated by glibenclamide – a case report
Autori
Rošin Grget, Kata ; Brailo Vlaho ; Mravk-Stipetić, Marinka ; Marinović, Branka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
Abstract of the 9th biennial Congress of the European Association of Oral Medicine
/ Baum, Bruce ; Scully, Crispian - Salzburg : Wiley-Blackwell, 2008, 36-36
Skup
9th biennial Congress of the European Association of Oral Medicine
Mjesto i datum
Salzburg, Austrija, 18.09.2008. - 20.09.2008
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
pemphigus; glibenclamide
Sažetak
Introduction: Pemphigus is autoimmune disease characterized by epithelial blistering affecting cutaneous and /or mucosal surfaces. Pemhigus might be outcome of the interaction between endogenous (genetic) and exogenous factors (such as drugs). Drugs most commonly associated with pemphigus are divided into three groups according their chemical structure: thiol drugs (sulfhydryl (SH)-containing) ; phenol drugs ; and nonthiol nonphenol drugs. We present a case of pemphigus developed after treatment with glibenclamide which is not exactly a thiol drug but has sulfur (S-) in its molecule. Chief complaint: 80 year old patient came to the Department of Oral medicine complaining of gingival soreness which lasted for 6 months. Medical history: His medical history revealed hypertension and diabetes mellitus for which he was taking amlodipine and glibenclamide. Oral disease history: Clinical examination revealed gingival erosions in his lower left molar area and intense redness in lower frontal gingival. Clinical presentation was consistent with desquamative gingivitis. Diagnostic procedures: Gingival biopsy was performed for histology and direct immunofluorescence. Histology was not specific, revealing mixed inflammatory infiltrate without acantholysis. Direct immunofluorescence revealed intercellular deposits of IgA. The finding was consistent with the diagnosis of Ig A mediated pemphigus. Treatment: Patient was prescribed betamethasone propionate in orabase and chlorhexidine solution 3 times daily for his lesions. New antidiabetic drug (metformin) was introduced. His lesions slowly healed within two months. Three months later at first recall, patient was asymptomatic. Conclusion: Our case confirmed that “ masked” thiol drugs (glibenclamide) could be involved in the pathogenesis of pemphigus.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Projekti:
108-0000000-0105 - Autoimune bulozne dermatoze u Republici Hrvatskoj (Marinović, Branka, MZOS ) ( CroRIS)
Ustanove:
Medicinski fakultet, Zagreb
Profili:
Kata Rošin-Grget
(autor)
Branka Marinović
(autor)
Vlaho Brailo
(autor)
Marinka Mravak-Stipetić
(autor)