Clinical Dermatology Review

LETTER TO EDITOR
Year
: 2020  |  Volume : 4  |  Issue : 2  |  Page : 186--188

Co-localization of alopecia areata and discoid lupus erythematosus


Keshavmurthy A Adya1, Arun C Inamadar1, Aparna Palit2,  
1 Department of Dermatology, Venereology and Leprosy, Shri B M Patil Medical College, Hospital and Research Center, BLDE (Deemed to be University), Vijayapur, Karnataka, India
2 Department of Dermatology and Venereology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India

Correspondence Address:
Arun C Inamadar
Department of Dermatology, Venereology and Leprosy, Shri B M Patil Medical College, Hospital and Research Center, BLDE (Deemed to be University), Vijayapur - 586 103, Karnataka
India




How to cite this article:
Adya KA, Inamadar AC, Palit A. Co-localization of alopecia areata and discoid lupus erythematosus.Clin Dermatol Rev 2020;4:186-188


How to cite this URL:
Adya KA, Inamadar AC, Palit A. Co-localization of alopecia areata and discoid lupus erythematosus. Clin Dermatol Rev [serial online] 2020 [cited 2020 Nov 27 ];4:186-188
Available from: https://www.cdriadvlkn.org/text.asp?2020/4/2/186/292480


Full Text



Sir,

Alopecia areata is a common T-cell mediated autoimmune disorder affecting the hair bulb, leading to non-scarring alopecia of varying degrees involving the hair bearing areas. The autoimmune nature of the disorder is supported by the fact that it may be coexistent with other cutaneous and systemic autoimmune disorders such as lichen planus, vitiligo, myasthenia gravis, and autoimmune thyroiditis.[1] While the coexistence of different autoimmune dermatoses is a relatively well known entity, co-localization of different autoimmune disorders is rare and only a handful of instances are reported in the literature. Herein, we describe a rare instance of anatomic co-localization of discoid lupus erythematosus (DLE) and alopecia areata.

A 30-year-old female presented with asymptomatic patchy hair loss on the scalp of 8 months' duration over which an occasionally itchy pigmented lesion had developed over the past 3 months. Examination revealed a well defined patch of non-scarring alopecia over the left parietal area measuring about 4 cm × 4 cm having a hyperpigmented plaque at the center with a cribriform surface and central depression measuring about 1 cm × 1 cm [Figure 1] and [Figure 2]. Non-contact polarized dermoscopy of both the alopecic area and the central pigmented plaque was performed using DermLite™ DL3 (3Gen, San Juan Capistrano, CA, USA). Dermoscopy of the alopecic area revealed black dots, short vellus hairs, yellow-brown dots, broken hairs, and tapering (exclamatory mark) hair [Figure 3]. Dermoscopy of the hyperpigmented plaque showed a dusky violaceous background, multiple follicular plugs, white rosettes, yellow-white streaks and globules, and shiny white lines [Figure 4]. The dermoscopic features of the alopecic area were quite specific of alopecia areata,[2],[3] and the dermoscopic diagnosis of DLE[4],[5] for the pigmented plaque was confirmed by histopathology which revealed epidermal atrophy, follicular plugs with perifollicular fibrosis, an interface reaction composed of band-like and aggregated infiltrate of mononuclear cells in the upper dermis, and upper dermal melanin incontinence [Figure 5].{Figure 1}{Figure 2}{Figure 3}{Figure 4}{Figure 5}

Coexistent of two or more autoimmune disorders is attributable to a common underlying immunopathology. Anatomic co-localization of such disorders is only sporadically documented. Co-localization of alopecia areata and lichen planus has been reported and has been attributed to a common underlying T-cell mediated autoimmune pathology.[6] Alopecia areata co-localized with vitiligo has also been described with a hypothesis that the CD4+ T-cell immune response mediating the former also targets the epidermal melanocytes, leading to the development of latter.[7],[8],[9] We could not find any documentation of co-localized DLE and alopecia areata in literature, which makes this report a novel one. This association can be explained as above by the similarity in the immunopathogenesis of DLE and alopecia areata. Both the disorders are mediated by T-cell immune response evidenced by the predominance of CD4+ T-cell population in the lesional infiltrate of both the disorders observed on immunohistochemistry.[10],[11]

Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.

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