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      Simultaneous dermatophytosis and keratomycosis caused by Trichophyton interdigitale infection: a case report and literature review

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          Abstract

          Background

          Dermatophytosis is a fungal infectious disease caused by dermatophytes, which produce protease and keratinase to digest keratin, leading to the colonization, invasion, and infection of the stratum corneum of the skin, hair shafts, and nails. Trichophyton interdigitale belongs to Trichophyton mentagrophytes complex, which is the common pathogen causing dermatophytosis. Fungal keratitis, also called keratomycosis, is an infectious disease of cornea.

          Case presentation

          Here, we report a case of simultaneous dermatophytosis and keratomycosis caused by Trichophyton interdigitale. A 67-year-old man presented with extensive erythema all over the body since 4 years ago, fungal infection of left eye for 2 years, and loss of vision in the eye. These symptoms had become aggravated in the last month. Dermatological examinations showed extensive erythematous plaques with clear borders and scales, scattered red papules with ulceration, and scabs throughout the body. Onychomycosis was observed on the nails of left hand, conjunctival infection with secretion and loss of vision were noted in left eye. Hyaline septate hyphae were observed under direct microscopic examination, fungal culture and internal transcribed spacer sequencing revealed T. interdigitale. Histopathological examination suggested infectious granuloma. A diagnosis of dermatophytosis and keratomycosis caused by T. interdigitale with loss of vision in left eye was made. The patient was treated with luliconazole cream (two applications per day) and itraconazole (100 mg, BID, PO). Complete clinical remission was achieved after 1 month. Subsequently, the patient underwent left eye enucleation in the ophthalmology department.

          Conclusions

          In the present study, we reported a case of simultaneous dermatophytosis and keratomycosis caused by T. interdigitale, and reviewed the literature on corneal infection caused by Trichophyton. A total of 10 articles with 45 patients were published between 1973 and 2018. The pathogen of 27 patient were identified to species level. There were T. schoenleinii (17), T. mentagrophytes (4), T. verrucosum (3), T. rubrum (1), T. erinacei (1), and T. interdigitale (1). Five patients had corneal trauma, one had contact lens use history. Direct microscopic examination, fungal culture, and analysis of physiological characteristics were the main methods of identification. Early diagnosis and prompt treatment may help improve the management and outcomes.

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          Most cited references30

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          A homozygous CARD9 mutation in a family with susceptibility to fungal infections.

          Chronic mucocutaneous candidiasis may be manifested as a primary immunodeficiency characterized by persistent or recurrent infections of the mucosa or the skin with candida species. Most cases are sporadic, but both autosomal dominant inheritance and autosomal recessive inheritance have been described. We performed genetic studies in 36 members of a large, consanguineous five-generation family, in which 4 members had recurrent fungal infections and an additional 3 members died during adolescence, 2 after invasive infection of the brain with candida species. All 36 family members were enrolled in the study, and 22 had blood samples taken for DNA analysis. Homozygosity mapping was used to locate the mutated gene. In the 4 affected family members (patients) and the 18 unaffected members we sequenced CARD9, the gene encoding the caspase recruitment domain-containing protein 9, carried out T-cell phenotyping, and performed functional studies, with the use of either leukocytes from the patients or a reconstituted murine model of the genetic defect. We found linkage (lod score, 3.6) to a genomic interval on chromosome 9q, including CARD9. All four patients had a homozygous point mutation in CARD9, resulting in a premature termination codon (Q295X). Healthy family members had wild-type expression of the CARD9 protein; the four patients lacked wild-type expression, which was associated with low numbers of Th17 cells (helper T cells producing interleukin-17). Functional studies based on genetic reconstitution of myeloid cells from Card9(-/-) mice showed that the Q295X mutation impairs innate signaling from the antifungal pattern-recognition receptor dectin-1. An autosomal recessive form of susceptibility to chronic mucocutaneous candidiasis is associated with homozygous mutations in CARD9. 2009 Massachusetts Medical Society
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            Epidemiology and aetiological diagnosis of corneal ulceration in Madurai, south India

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              Ocular fungal infections.

              Microbiology, clinical perspective of ocular fungal infections, and the experimental models were overviewed. Review of published studies were evaluated and personal experience was mentioned. In this review, clinical features of keratitis and endogenous and exogenous endophthalmitis are also mentioned, but this article mainly focused on laboratory diagnosis and the experimental models of ophthalmic mycoses. Fungal infections were discussed according to the anatomical part of the eye involved in the disease. Trauma is the most important predisposing cause; the species of Fusarium, Aspergillus, and Candida are the most frequently isolated organisms. Laboratory methods, such as culture, remains the cornerstone of diagnosis; direct microscopic detection of fungal structures in ocular samples permits a rapid presumptive diagnosis. New approaches, such as serological and molecular methods, have been widely used in recent years. A variety of antifungals have been evaluated in the therapy of this condition. Experimental models would facilitate investigations exploring the pathophysiology, cell biology, genetics, immunology, and therapy of this disease. Fungal infections of the eye continue to be an important cause of ocular morbidity, particularly in the developing world. Understanding ocular infections will improve the outcome of this condition.
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                Author and article information

                Contributors
                zhangmr16@mails.jlu.edu.cn
                jianglanxiang@soho.com
                13039123758 , lifuqiu1234@126.com
                yangchunxu0701@sina.com
                tuzicaoye@163.com
                wangbing513562@163.com
                Journal
                BMC Infect Dis
                BMC Infect. Dis
                BMC Infectious Diseases
                BioMed Central (London )
                1471-2334
                21 November 2019
                21 November 2019
                2019
                : 19
                : 983
                Affiliations
                GRID grid.452829.0, Department of Dermatology, , the Second Hospital of Jilin University, ; No. 218, Ziqiang street, Nanguan district, Changchun, 130000 China
                Article
                4612
                10.1186/s12879-019-4612-0
                6873498
                31752715
                36459363-3178-4d5c-89f0-5e6d132bdd7a
                © The Author(s). 2019

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 8 November 2018
                : 31 October 2019
                Categories
                Case Report
                Custom metadata
                © The Author(s) 2019

                Infectious disease & Microbiology
                dermatophytosis,keratomycosis,trichophyton interdigitale,case report

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