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. 2024 Aug 21;10(3):e175.
doi: 10.1097/JW9.0000000000000175. eCollection 2024 Oct.

Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis

Affiliations

Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis

Anissa Zaouak et al. Int J Womens Dermatol. .

Abstract

Background: Autosomal recessive congenital ichthyosis (ARCI) is a rare genodermatosis categorized among nonsyndromic ichthyoses. While ARCI patients often manifest hair abnormalities, their impact on the quality of life remains underreported in the literature.

Objective: This study aims to comprehensively characterize the clinical and trichoscopic findings of alopecia in ARCI patients.

Methods: A prospective study spanning from January 2019 to December 2021 (3 years) was conducted at the Dermatology Department of Habib Thameur Hospital, Tunis, Tunisia. Clinical and trichoscopic examinations were performed on the hair of the participants, with molecular studies conducted on 15 patients.

Results: The study included 30 patients, predominantly female (male/female = 0.58), with a mean age of 20 years. Twenty-eight patients were born from consanguineous marriages. Lamellar ichthyosis was observed in 22 cases, while congenital ichthyosiform erythroderma and bathing suit ichthyosis were each present in 4 cases. The ARCI severity score, assessed using the Visual Index For Ichthyosis Severity scale, had a mean value of 15 (4-28). Alopecia emerged as a prominent finding in 11 patients, presenting as hairline recession (13%), multiple patchy alopecia (27%), and alopecia of the eyebrows (13%). Trichoscopic findings included interfollicular and perifollicular scaling, perifollicular lamellar hyperkeratosis, peripilar casts, interfollicular erythema, loss of hair openings, predominance of single hair follicles, broken hair, vellus hair, anisotrichosis, pili torti, dystrophic hair, and comma hair. Several trichoscopic findings showed statistically significant associations with the severity of ARCI.

Limitations: In our study, we only included 30 patients due to the rarity of this genodermatosis.

Conclusion: Contrary to previous perceptions, alopecia is a notable finding in ARCI, particularly in patients with a severe form. This study provides a detailed characterization of alopecia in ARCI, shedding light on its prevalence and associated trichoscopic features, thereby enhancing our understanding of this dermatological condition.

Keywords: alopecia; hair; ichthyosis.

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Conflict of interest statement

None.

Figures

Fig. 1.
Fig. 1.
(A) Multiple alopecic patches of the scalp associated with diffuse scaling and thin and brittle hair. (B) Circumferential hairline recession associated with brown lamellar scales on the scalp. (C) Hairline recession of the posterior scalp associated with brown lamellar scales. (D) Hair line recession of the frontal scalp associated with yellow scales.
Fig. 2.
Fig. 2.
(A) Alopecia of the eyebrows. (B) Fishing float keratotic plugs and 3D bubble yellow dots (Dermlite DL4 × 20). (C) Interfollicular erythema and interfollicular scales, and perifollicular lamellar keratosis (Dermlite DL4 × 20). (D) Transparent proximal hair shaft emergence (Dermlite DL4 × 20). (E) Peripilar casts (Dermlite DL4 × 20).

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