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Updated: Jun 23, 2026

Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Extensive tinea in a patient with severe combined immunodeficiency
Rafael Jiménez-Puya1, C Vázquez-Bayo, A Rodriguez-Bujaldón
1Service of Dermatology, University Hospital Reina Sofía, Córdoba, Spain. rafaeljpuya@hotmail.com
Severe combined immunodeficiency (SCID) is a rare genetic disorder affecting T and B cell immunity. This case highlights an unusual widespread dermatophyte skin infection in a SCID patient, expanding the known clinical presentations of this condition.
Area of Science:
- Immunology
- Genetics
- Dermatology
Background:
- Severe combined immunodeficiency (SCID) comprises a group of genetic disorders impairing T and B cell immunity.
- While X-linked recessive SCID is most prevalent, autosomal recessive forms and spontaneous mutations also occur.
- SCID patients commonly experience nosocomial infections, but dermatophyte infections are infrequent.
Observation:
- A case of SCID presented with a rare and extensive skin infection.
- The infection was caused by the dermatophyte species *Trichophyton mentagrophytes*.
- This presentation is atypical for known SCID manifestations.
Findings:
- The study details a specific case linking SCID to a widespread *Trichophyton mentagrophytes* infection.
- This association expands the spectrum of opportunistic infections observed in SCID patients.
- The genetic basis of SCID underlies the compromised immune response.
Implications:
- Recognizing this atypical presentation can aid in earlier diagnosis of SCID.
- Understanding SCID-associated infections is crucial for patient management and treatment strategies.
- Further research may elucidate the specific immune defects predisposing SCID patients to dermatophyte infections.
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