Literature DB >> 29742560

Two Cases of Chronic Candidiasis in Keratitis-Ichthyosis-Deafness Syndrome.

Diana Bartenstein1, Hye Jin Chung2, Sadaf Hussain3.   

Abstract

Keratitis-ichthyosis-deafness (KID) syndrome is a rare genodermatosis that typically results from mutations of the GJB2 gene or, less commonly, the GJB6 gene. Patients with KID syndrome are at higher risk of malignancy and infections. Here, we present 2 patients with KID syndrome who developed verrucous plaques. Given that patients with KID syndrome are at high risk of developing squamous cell carcinoma, biopsies were performed. Both cases revealed histologic findings of marked papillomatous epidermal hyperplasia with numerous fungal spores and pseudohyphae in the stratum corneum. For one case, daily oral fluconazole was initiated. The patient demonstrated dramatic resolution of his foot plaques over the course of 2 years. These cases highlight that, for the dermatopathologist, chronic fungal infection should be sought for verrucous plaques in patients with KID syndrome as, if present, this finding may alter treatment and quality of life.

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Year:  2018        PMID: 29742560     DOI: 10.1097/DAD.0000000000001178

Source DB:  PubMed          Journal:  Am J Dermatopathol        ISSN: 0193-1091            Impact factor:   1.533


  1 in total

1.  Congenital ichthyosis associated with Trichophyton rubrum tinea, imitating drug hypersensitivity reaction.

Authors:  Eszter Szlávicz; Csongor Németh; Éva Szepes; Csaba Gyömörei; Rolland Gyulai; Zsuzsanna Lengyel
Journal:  Med Mycol Case Rep       Date:  2020-05-29
  1 in total

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