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    The effect of gastric Helicobacter pylori eradication on recurrent aphthous stomatitis
    (Wiley, 2008) Karaca, Semsettin; Seyhan, Muammer; Senol, Mustafa; Harputluoglu, M. Muhip; Ozcan, Atilla
    Background Helicobacter pylori (H. pylori) has been suggested to be associated with recurrent aphthous stomatitis (RAS) as well as many other diseases. Methods We conducted a prospective study on a total of 23 patients with RAS to investigate the relationship between H. pylori and RAS as well as the effect of eradication therapy on the recurrence. All patients underwent endoscopic examination and gastric biopsy. The biopsy materials were examined histopathologically whether they contained H. pylori or not. The density of H. pylori was also noted. The patients with H. pylori infection were followed up for up to 1 year after starting the eradication therapy. Results Gastric mucosal H. pylori colonization was (+) in 39%, (++) in 39%, (+++) in 9%, and (-) in 13% of the patients, respectively. There were statistically significant decreases in the recurrence rate and amelioration time of RAS by eradication therapy. There were no significant correlations among the intensity of H. pylori with the recurrence rate, number, diameter, and amelioration time of the lesions in 1-year follow-up. Conclusions We concluded that eradication of H. pylori may have reducing effects on the recurrence and amelioration period of the RAS.
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    Intertriginous plasmacytosis with plasmoacanthoma: report of a typical case and review of the literature
    (Blackwell Publishing, 2008) Senol, Mustafa; Ozcan, Atilla; Aydin, N. Engin; Hazneci, Ersoy; Turan, Nergiz
    Clinical manifestations of benign (reactive) plasma cell proliferations of the skin and mucosa consist of a relatively rare and distinct group in dermatologic disorders. They have generally been named according to their localization. We report a typical case of mucocutaneous plasmacytosis located on intertriginous areas of the skin as well as mucosa with a perianal tumoral mass diagnosed as plasmoacanthoma. To our knowledge, this is the first detailed case report, at least in English literature.