Zaouak Anissa, Jouini Wafa, Abdessalem Ghaith, Abdelhak Sonia, Hammami Houda, Charfeddine Cherine, Fenniche Samy
Dermatology Department, Habib Thameur Hospital, Tunis, Tunisia.
Biomedical Genomics and Oncogenetics Laboratory, Institut Pasteur de Tunis, Tunis, Tunisia.
Int J Womens Dermatol. 2024 Aug 21;10(3):e175. doi: 10.1097/JW9.0000000000000175. eCollection 2024 Oct.
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.
This study aims to comprehensively characterize the clinical and trichoscopic findings of alopecia in ARCI patients.
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.
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.
In our study, we only included 30 patients due to the rarity of this genodermatosis.
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.
常染色体隐性遗传性先天性鱼鳞病(ARCI)是一种罕见的遗传性皮肤病,属于非综合征性鱼鳞病。虽然ARCI患者常表现出毛发异常,但文献中对其对生活质量的影响报道较少。
本研究旨在全面描述ARCI患者脱发的临床和毛发镜检查结果。
2019年1月至2021年12月(3年),在突尼斯突尼斯市哈比卜·塔默尔医院皮肤科进行了一项前瞻性研究。对参与者的头发进行了临床和毛发镜检查,并对15名患者进行了分子研究。
该研究纳入了30名患者,以女性为主(男/女 = 0.58),平均年龄为20岁。28名患者出生于近亲结婚家庭。观察到22例板层状鱼鳞病,4例先天性鱼鳞病样红皮病和4例泳衣样鱼鳞病。使用鱼鳞病严重程度视觉指数评估的ARCI严重程度评分平均值为15(4 - 28)。11名患者出现脱发这一突出表现,表现为发际线后移(13%)、多发性斑秃(27%)和眉毛脱落(13%)。毛发镜检查结果包括毛囊间和毛囊周围脱屑、毛囊周围板层状角化过度、毛周角质套、毛囊间红斑、毛囊开口缺失、单毛囊为主、断发、毳毛、毛发粗细不均、扭曲发、营养不良性毛发和逗号发。多项毛发镜检查结果与ARCI的严重程度存在统计学上的显著关联。
在我们的研究中,由于这种遗传性皮肤病的罕见性,我们仅纳入了30名患者。
与以往的认识相反,脱发是ARCI中的一个显著表现,尤其是在重症患者中。本研究详细描述了ARCI中的脱发情况,揭示了其患病率和相关的毛发镜特征,从而增进了我们对这种皮肤病的理解。