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A Clinical and Histopathological study on the Localized Recessive Kystrophic Type of Epidermoysis Bullosa

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¼­±æÁ¶ ( Suh Gil-Jo ) - Á¶¼±´ëÇб³ Ä¡°ú´ëÇÐ Ä¡ÁÖ°úÇб³½Ç
±èº´¿Á ( Kim Byung-Ok ) - Á¶¼±´ëÇб³ Ä¡°ú´ëÇÐ Ä¡ÁÖ°úÇб³½Ç
ÇÑ°æÀ± ( Han Kyung-Yoon ) - Á¶¼±´ëÇб³ Ä¡°ú´ëÇÐ Ä¡ÁÖ°úÇб³½Ç

Abstract


A fcnulle. patient, 24 year-old, who had been suffered from gingival bleeding during tooth brushing, burning sensation on ulcerated oral mucosa, and blisters and erosive ulcers on extermities was examined clinically and histopathologically.
Radiographs showed dental caries on maxillary anterior teeth and generalized resorption of alveolar bone.
Subepidermal cleavage beneath laminar densa in the superficial region of dermis was observed by Light microscope.
According to the clinical, radiographical and histological findings, final diagnosis was established as the lozalized recessive dystrophic type of epidermolysis bullosa.
EpidcrmolN sis Bullosa is a rare hereditary disease with the common characteristic of 10 marked skin fragility and blister formation following seemingly minor or insignificant trauma to the skin and mucosa ; as such, it is referreu to as a :nechanobullous disease.
Patient¢¥s complaint was gradually subsided by periodic plaque control and local therapy, but continuous careful maintenance care was recommended.

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