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1.
Pediatrics ; 136(5): e1386-9, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26482671

ABSTRACT

Blastomyces dermatitidis is a dimorphic fungus endemic to much of North America, particularly the soils of the midwestern and southeastern United States. Human infection typically occurs through inhalation of airborne conidia, which can be followed occasionally by dissemination to the skin, bone, genitourinary system, and central nervous system. A hallmark of the pathogen is that it can cause disease in both immunocompetent and immunosuppressed populations. Blastomycosis is rare in pediatric patients, with cutaneous manifestations occurring even less frequently. Here, we report the case of a 9-year-old boy on iatrogenic immunosuppression with infliximab and methotrexate for juvenile idiopathic arthritis who presented with a nonhealing, indurated plaque of his right ear with significant superficial yellow crusting in the absence of constitutional symptoms. After failing a prolonged course of topical and oral antibiotic therapy, biopsy and tissue culture revealed Blastomyces dermatitidis infection. The area cleared after treatment with oral fluconazole and withdrawal of infliximab. To our knowledge, this is the first report of a pediatric patient developing an infection with B dermatitidis after initiation of therapy with a tumor necrosis factor-α inhibitor. This case also highlights an unusual morphology of cutaneous blastomycosis in an iatrogenically immunosuppressed child.


Subject(s)
Antirheumatic Agents/adverse effects , Arthritis, Juvenile/drug therapy , Blastomycosis/chemically induced , Infliximab/adverse effects , Antirheumatic Agents/therapeutic use , Child , Female , Humans , Infliximab/therapeutic use , Male
2.
J Am Acad Dermatol ; 71(1): 1.e1-8; quiz 1.e8-9, 10, 2014 Jul.
Article in English | MEDLINE | ID: mdl-24947698

ABSTRACT

Tumor necrosis factor-alfa levels are linked to disease severity in patients with inflammatory conditions, such as psoriasis. Inhibitors of this cytokine are commonly used with significant success in the treatment of such inflammatory disorders. Their use, however, can be plagued by infectious complications. An awareness of potential infections associated with these therapies is critical in order to maximize preventive efforts both before and during therapy. This review provides a guide for dermatologists caring for patients in need of this type of biologic therapy to preemptively address the infectious risks. Part I of this continuing medical education article reviews background information on the various infectious risks associated with tumor necrosis factor inhibitor therapy and appropriate historical data to obtain in the context of pretherapy evaluations.


Subject(s)
Biological Therapy/adverse effects , Communicable Diseases/complications , Skin Diseases/complications , Skin Diseases/drug therapy , Tumor Necrosis Factor-alpha/antagonists & inhibitors , Antibodies, Monoclonal, Humanized/adverse effects , Blastomycosis/chemically induced , Blastomycosis/complications , Coccidioidomycosis/chemically induced , Coccidioidomycosis/complications , Communicable Diseases/chemically induced , Communicable Diseases/immunology , Disease Progression , Endemic Diseases , Histoplasmosis/chemically induced , Histoplasmosis/complications , Humans , Medical History Taking , Psoriasis/complications , Psoriasis/drug therapy , Risk Assessment , Tuberculosis/chemically induced , Tuberculosis/complications , Tumor Necrosis Factor-alpha/immunology , Ustekinumab
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