Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
Collagen VI-related myopathies are characterized by severe muscle involvement and skin involvement (keratosis pilaris and impaired healing with the development of abnormal scars, especially keloids). Scalp involvement and hair loss have not been reported among cutaneous changes associated with collagen VI mutations. The aim of this study is to describe the clinical, trichoscopic, and histological findings of the scalp changes in patients affected by COL VI mutations and to estimate their prevalence. Patients with Ullrich congenital muscular dystrophy were enrolled and underwent clinical and trichoscopic examinations and a scalp biopsy for histopathology. Five patients were enrolled, and all complained of hair loss and scalp itching. One patient showed yellow interfollicular scales with erythema and dilated, branched vessels, and the histological findings were suggestive of scalp psoriasis. Two patients presented with scarring alopecia patches on the vertex area, and they were histologically diagnosed with folliculitis decalvans. The last two patients presented with scaling and hair thinning, but they were both diagnosed with folliculitis and perifolliculitis. Ten more patients answered to a “scalp involvement questionnaire”, and six of them confirmed to have or have had scalp disorders and/or itching. Scalp involvement can be associated with COL VI mutations and should be investigated.
Starace, Michela; Pampaloni, Francesca; Bruni, Francesca; Quadrelli, Federico; Cedirian, Stephano; Baraldi, Carlotta; Misciali, Cosimo; Di Martino, Alberto; Sabatelli, Patrizia; Merlini, Luciano; and Piraccini, Bianca Maria, "Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype" (2023). Department of Dermatology and Cutaneous Biology Faculty Papers. Paper 180.
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This article is the author's final published version in International Journal of Molecular Sciences, Volume 24, Issue 7, 2023, Article number 6678.
The published version is available at https://doi.org/10.3390/ijms24076678. Copyright © 2023 by the authors. Licensee MDPI, Basel, Switzerland.