Clinical Course, Antifungal Susceptibility, and Genomic Sequencing of <i>Trichophyton indotineae</i>

JAMA Dermatology
Open Access

Clinical Summary

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What was studied

A retrospective cohort case series from six New York City centers (May 2022–May 2023) examined 11 patients with confirmed Trichophyton indotineae, correlating clinical features with antifungal minimum inhibitory concentrations, squalene epoxidase mutations, and whole‑genome sequencing; outcome was improvement or resolution at last follow‑up.

Key findings

Terbinafine (250 mg daily) failed in 7 patients, and their isolates carried SQLE L393S or F397L with elevated terbinafine MICs ≥0.5 μg/mL. Improvement occurred in 2/4 on fluconazole and 2/5 on griseofulvin (no outcome–MIC correlation); 5/7 on itraconazole cleared or improved (2/7 lost to follow‑up or stopped), and U.S. isolates formed a distinct cluster from Indian isolates; 9/11 reported travel to Bangladesh.

Study limitations

Small sample (n=11) and single‑city, multi‑center case series limit generalizability. Uncontrolled, retrospective design with heterogeneous treatments and incomplete follow‑up (2 of 7 on itraconazole lost or stopped) constrains outcome interpretation.

Clinical implications

Expect terbinafine failure associated with SQLE mutations and elevated MICs in T indotineae; in this series, itraconazole led to clearance or improvement in 5 of 7 treated patients. Take a travel history—most patients reported travel to Bangladesh—and consider susceptibility testing when terbinafine fails.