Pregled bibliografske jedinice broj: 1098033
Tinea incognita in a patient with CREST Syndrome
Tinea incognita in a patient with CREST Syndrome // CD Rom
Istanbul, 2013. str. /-/ (poster, međunarodna recenzija, sažetak, stručni)
CROSBI ID: 1098033 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Tinea incognita in a patient with CREST Syndrome
Autori
Gorgievska-Sukarovska, Biljana ; Skerlev, Mihael ; Bardek, Ivana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
CD Rom
/ - Istanbul, 2013, /-/
Skup
22nd Congress of the European Academy of Dermatology and Venereology
Mjesto i datum
Istanbul, Turska, 02.10.2013. - 06.10.2013
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Tinea incognita ; CREST Syndrome
Sažetak
Introduction and Objectives: : Tinea incognita is an initially unrecognized dermatophyte infection, usually modified by the inappropriate topical or systemic corticosteroid therapy. Moreover, cases of tinea incognita caused by topical immunomodulators such as pimecrolimus and tacrolimus have been recently reported. We report case of an extensive tinea incognita caused by zoophylic dermatophyte Trichophyton mentagrophytes (var. granulosa) in a patient with CREST syndrome. Materials and Methods: Forty-nine-year-old female patient has been referred to our Department due to the extensive erythematous, not well demarcated lesions on the trunk, neck and arms. Ichtyosiform scales and excoriations were observed, as well. Prior to this visit, the lesions had been unsuccessfully treated with topical betamethasone cream. Very intensive pruritus urged the patient to visit dermatologist. Fifteen years before, the patient was diagnosed with CREST syndrome, with biliary cirrhosis and had been continuously receiving systemic steroids. Eventually, the maintenance dose was 10 mg of prednisone daily . Apart of the previously described skin lesions, the physical examination revealed also sclerodactyly and calcinosis of the fingers, with yellowish discoloration of the nails. Numerous teleangiectasias were spread over the face, neck, upper trunk and even lips. Results: Direct microscopic potassium hydroxide (KOH) examination of the skin scrapings was positive revealing fungal hyphae and Trichophyton mentagrophytes (var. granulosa) was confirmed by culture on the glucose-modified Sabouraud medium. Direct examination and fungal culture of the nails were negative. The topical treatment with terbinafine cream was initiated. Systemic antimycotic therapy was not administered because of the very good response on the topical therapy and because of high level of liver enzymes, as well. After the four weeks of treatment, a complete clinical and mycological regression was observed. Conclusion: Immunocompromized patients are susceptible to dermatophyte infections with atypical clinical presentation. Sometimes, clinical appearance is bizarre and difficult to recognize. Therefore, close monitoring and mycological skin examination is recommended in order to avoid misdiagnosis and to give the patient the best chance of cure.
Izvorni jezik
Engleski
POVEZANOST RADA
Ustanove:
Medicinski fakultet, Zagreb,
Klinički bolnički centar Zagreb,
Opća bolnica Zabok