Cutaneous mucormycosis in a patient with Hailey-Hailey disease (benign familial pemphigus) - first reported case

Joseph David Cooper, Dennis W Adams, Lucy Studemeister, Allyson E Sorensen, Christopher Hull · 2026

Read Cutaneous mucormycosis in a patient with Hailey-Hailey disease (benign familial pemphigus) - first reported case by Joseph David Cooper, Dennis W Adams, Lucy Studemeister, Allyson E Sorensen, Christopher Hull (2026) in the Tower of Babel, a free online library of public-domain works preserved in clean, searchable text. No sign-up. The full text is served as a plain-text file at a predictable URL, where text is present: https://antarctic-labs.com/tower-of-babel/pmc-13563460.txt.

Description

Joseph David Cooper and four co-authors report a dangerous fungal invasion in skin already broken by a rare genetic blistering disease, in this 2026 case report. Their patient lives with Hailey-Hailey disease, benign familial pemphigus, which leaves raw, fragile patches where skin rubs. Into that opening came mucormycosis, an aggressive mold infection, growing directly in the skin.

The diagnosis was nailed down two ways: microbiological culture grew the fungus, and tissue pathology showed it invading. Treatment paired the two standard weapons, prompt surgery to cut away infected and dead tissue, and complementary antifungal drugs. The patient improved. To the authors' knowledge, this pairing of the two rare conditions has never been reported before. The report contributes on both fronts: how a fast-moving mold exploits chronically wounded skin, and how quickly combined treatment must move when it does.

Catalog record

CREATORJoseph David Cooper, Dennis W Adams, Lucy Studemeister, Allyson E Sorensen, Christopher Hull
YEAR2026
COLLECTIONPAPERS
FORMATTXT
FILE SIZE17 KB
VERSION1.0
LICENSECC BY 4.0
RIGHTSCC BY
SOURCEEurope PMC

Source: https://europepmc.org/articles/PMC13563460

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