Chronic mucocutaneous candidiasis and systemic lupus erythematosus: a new variant of chronic mucocutaneous candidiasis?
Author(s) -
Dewton de Moraes Vasconcelos,
Maurício Domingues Ferreira,
Patrícia de Campos Pieri,
Alberto José da Silva Duarte
Publication year - 2012
Publication title -
medical mycology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.004
H-Index - 86
eISSN - 1460-2709
pISSN - 1369-3786
DOI - 10.3109/13693786.2011.622305
Subject(s) - chronic mucocutaneous candidiasis , mucocutaneous zone , medicine , immunology , systemic candidiasis , dermatology , pathology , disease , corpus albicans , antifungal
Chronic mucocutaneous candidiasis (CMC) is characterized by susceptibility to Candida infection of skin, nails, and mucous membranes. Autoimmune endocrinopathies are common in CMC patients, but there are no reports of the involvement of systemic autoimmune disorders. We present here the first case of this kind of association in a patient with an autosomal dominant variant of CMC. The individual had had this disorder since childhood and systemic lupus erythematosus with secondary antiphospholipid syndrome, as well as renal, articular and hepatic manifestations without thymoma.
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