Your browser doesn't support javascript.
loading
Novel CARD9 mutation in a patient with chronic invasive dermatophyte infection (tinea profunda).
Nazarian, Rosalynn M; Lilly, Evelyn; Gavino, Christina; Hamilos, Daniel L; Felsenstein, Donna; Vinh, Donald C; Googe, Paul B.
Affiliation
  • Nazarian RM; Department of Pathology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Lilly E; Department of Dermatology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Gavino C; Department of Medicine, McGill University Health Center, and Infectious Disease Susceptibility Program, Research Institute-McGill University Health Centre, Montreal, Quebec, Canada.
  • Hamilos DL; Department of Medicine, Division of Rheumatology, Allergy, and Immunology, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Felsenstein D; Department of Medicine, Infectious Disease Unit, Massachusetts General Hospital and Harvard Medical School, Boston, Massachusetts.
  • Vinh DC; Department of Medicine, McGill University Health Center, and Infectious Disease Susceptibility Program, Research Institute-McGill University Health Centre, Montreal, Quebec, Canada.
  • Googe PB; Department of Dermatology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
J Cutan Pathol ; 47(2): 166-170, 2020 Feb.
Article in En | MEDLINE | ID: mdl-31469433
ABSTRACT
Caspase Recruitment Domain Family Member 9 (CARD9) is an adaptor molecule that drives antifungal activity of macrophages and neutrophils in the skin. Autosomal recessive loss-of-function mutations in CARD9 confer increased susceptibility to invasive disease with select fungi in non-immunosuppressed patients. We report on a patient with X-linked ichthyosis complicated by chronic cutaneous invasive dermatophyte infection. We identified a previously reported c.271T>C (p.Y91H) mutation and a novel intronic c.1269+18G>A mutation in CARD9 underlying recurrent deep dermatophytosis in this patient despite various antifungals for over three decades. Our case highlights susceptibility to invasive dermatophytosis related to autosomal recessive CARD9 deficiency and illustrates the range of CARD9 mutations to be pursued in immunocompetent patients with unexplained deep dermatophyte infections. Further studies are needed to define the best therapeutic regimen.
Subject(s)
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tinea Capitis / Candidiasis, Chronic Mucocutaneous / Genetic Diseases, X-Linked / CARD Signaling Adaptor Proteins / Loss of Function Mutation Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: J Cutan Pathol Year: 2020 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Tinea Capitis / Candidiasis, Chronic Mucocutaneous / Genetic Diseases, X-Linked / CARD Signaling Adaptor Proteins / Loss of Function Mutation Type of study: Prognostic_studies Limits: Adult / Humans / Male Language: En Journal: J Cutan Pathol Year: 2020 Type: Article