We present the case of a 77-year-old female with a rare genital and anoperineal granulomatous cutaneous manifestation resembling cheilitis granulomatosa Miescher. The typical histological findings of epithelioid cell granulomas were localized in the vulva and anoperineal region; the latter manifestation has not yet been described. Based on our personal observations and a review of the literature, the clinical and histological features of vulvitis granulomatosa are described.
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http://dx.doi.org/10.1159/000247761 | DOI Listing |
JAAD Case Rep
September 2022
Department of Dermatology, Indiana University School of Medicine, Indianapolis, Indiana.
Clin Case Rep
April 2022
Department of Dermatology, Faculty of Medicine Saga University Saga Japan.
Crohn's disease (CD) of the vulva is a rare and under-recognized condition. Since vulvar lesions may precede the diagnosis of digestive CD in approximately 25% of all cases, the coexistence or future onset of CD should be considered regardless of the gastrointestinal symptoms, even for pediatric patients.
View Article and Find Full Text PDFJAAD Case Rep
June 2020
Department of Dermatology, King Abdulaziz University, Jeddah, Saudi Arabia.
J Dermatol
October 2005
Department of Dermatology, Kitasato University School of Medicine, Kanagawa, Japan.
Merkersson-Rosenthal syndrome (MRS) is characterized by cheilitis or pareitis granulomatosa, facial palsy, and fissured tongue. Sometimes the forehead, eyelids and chin are involved, and occasionally genital lesions are present. A vulval lesion of MRS is named vulvitis granulomatosa.
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