Annular psoriasis in a child: A rare entity

Sokaina Chhiti, Sara Elloudi, Fatimazahra Hashas, Zakia Douhi, Meryem Soughi, Hanane Baybay, Fatima Zahra Mernissi

Department of Dermatology, University Hospital Hassan II Fez, Morocco

Corresponding author: Sokaina Chhiti, MD, E-mail: drsokaina.chhiti@gmail.com

How to cite this article: Chhiti S, Elloudi S, Douhi Z, Soughi M, Baybay H, Mernissi FZ. Annular psoriasis in a child: A rare entity. Our Dermatol Online. 2025;16(2):184-185.
Submission: 18.04.2023; Acceptance: 16.10.2023
DOI: 10.7241/ourd.20252.16

Citation tools: 

Related Content

Copyright information

© Our Dermatology Online 2025. No commercial re-use. See rights and permissions. Published by Our Dermatology Online.


ABSTRACT

Psoriasis is a chronic inflammatory disease with varied clinical presentations among patients, ranging from small drop lesions to life-threatening erythroderma. Annular psoriasis remains a rare entity, whose annular appearance is either primary or secondary to treatment or due to the evolution of pustular psoriasis. Herein, we report the unusual case of a ten-year-old child with de novo annular psoriasis with no history of preceding pustular lesions and any other treatment. This is a rare entity that manifests as annular plaques without a pustule confounding several pathologies. We describe a primary form of psoriasis without pustules with a good and favorable course under treatment.

Key words: Psoriasis, Annular, Pustule, Children


INTRODUCTION

Psoriasis is a chronic inflammatory condition. It usually manifests as erythematous, scaly patches with a predilection for the elbows, knees, extensor extremities, scalp, and lumbosacral regions. There are several clinical features that may lead to diagnostic confusion in some situations. Annular morphology is a rare presentation of this disease and must be differentiated on a clinical/pathological basis from other diseases that usually produce annular lesions. Herein, we report the case of a child who presented with atypical, mainly annular, hypopigmented lesions of psoriasis present since the age of twelve years.

CASE REPORT

A twelve-year-old boy, with no notable pathological history, consulted for diffuse, pruritic, erythematous, scaly lesions on the body that had been evolving for eight months in flare-ups and remissions, for which he had applied several topical treatments, notably antimycotics, without any improvement. He reported that the lesions had had this clinical appearance since the beginning. There was no notion of pustular lesions, nor of pustules or scaling reminiscent of pre-existing pustules. On clinical examination, the child was in good general condition with multiple, silvery, erythematous plaques with scaly surfaces and hypopigmented centers, located preferentially on the axillary folds, trunk, and lower limbs, sparing the face (Figs. 1a and 1b). Broq’s methodical scraping was positive, Wood’s light was negative, and the rest of the clinical examination was unremarkable. A skin biopsy (Fig. 2) confirmed the diagnosis of psoriasis and the patient was initiated on methotrexate with improvement.

Figure 1: (a) Multiple annular plates with centrifugal extension at the trunk level. (b) Multiple annular scaly patches on the lower limbs.
Figure 2: Histological section showing a typical aspect of psoriasis.

DISCUSSION

Psoriasis in children may present with several clinical presentations, including typical plaques, guttate, inverted, palmoplantar, linear, and seborrheic forms [1,2], among which plaque psoriasis is the most common. The annular form has been described in the literature as a resolution of plaques following inadequate treatment or as a presentation of pustular psoriasis [3]. Primary non-pustular, annular, psoriatic plaques have been mentioned in some reports. In a review of 1262 children with psoriasis, Morris et al. [4] mentioned a type of non-pustular annular psoriasis. Abel et al. [5] explained that the central parts of some psoriatic plaques may involute after topical treatment and, as a result, transient circular lesions form. Guill et al. reported two cases with such a clinical presentation and typical psoriatic histopathology [6]. Terunuma et al. described an acute annular psoriatic rash with histology showing the presence of psoriatic changes yet no pustules, in contrast to annular pustular psoriasis [7]. Primary plaque psoriasis, which is exclusively annular, has been rarely described in the literature, and our case had a de novo presentation with lesions characteristic of plaque psoriasis, yet with a distinct central clearing and an annular pattern of the plaques. This was unusual as the plaques were consistently annular and not the result of any previous treatment. Annular plaque psoriasis has a broad differential diagnosis and may be confused with other entities, such as dermatophyte of glabrous skin, pityriasis rosea, subacute cutaneous lupus erythematosus, centrifugal erythema annulare, hypopigmented vitiligo, granuloma annulare, serpiginous perforating elastosis, sarcoidosis, nummular eczema, and urticaria [8]. These entities may be distinguished on the basis of histopathological findings. Although a rare entity, primary ring psoriasis occurs in all ages, yet affects a relatively higher proportion of the younger population. It has a more benign course than pustular psoriasis, which may be accompanied by fever and leukocytosis or even general impairment. Complete resolution with treatment usually occurs within days to weeks yet may take several months [9].

CONCLUSION

This case highlights a rare presentation of a highly common condition and shows that psoriasis may be retained in the differential diagnosis of annular plaques.

Consent

The examination of the patient was conducted according to the principles of the Declaration of Helsinki.

The authors certify that they have obtained all appropriate patient consent forms, in which the patients gave their consent for images and other clinical information to be included in the journal. The patients understand that their names and initials will not be published, and due effort will be made to conceal their identity, but that anonymity cannot be guaranteed.

REFERENCES

1. Ferrándiz C, Pujol RM, García-Patos V, Bordas X, Smandía JA. Psoriasis of early and late onset:A clinical and epidemiologic study from Spain. J Am Acad Dermatol. 2002;466:867-73.

2. Alanazi S, Arafat N. Unusual presentation of psoriasis. Our Dermatol Online. 2018;9:187-9.

3. Khurana A, Groverb C. Primary annular plaque psoriasis:A rare entity. Tropical Clinics in Dermatology. 2013.

4. Morris A, Rogers M, Fischer G, Williams K. Childhood psoriasis:A clinical review of 1262 cases. Ped Dermatol, 2001;18:188-98.

5. Demis DJ. Clinical Dermatology, Philadelphia:JB Lippincott, 1972.

6. Guill CL, Hoang MP, Carder KR. Primary annular plaque-type psoriasis. Pediatr Dermatol. 2005;22:15-8.

7. Terunuma A, Takahashi K, Sakakibara A, Aiba S, Tagami H. Annular psoriasiform eruption with lymphocytic infiltration of the epidermis:A variant of acute psoriasis. Dermatology. 1992;185:156-9.

8. Liao PB, Rubinson R, Howard R, Sanchez G, Frieden IJ. Annular pustular psoriasis:Most common form of pustular psoriasis in children:Report of three cases and review of the literature. Pediatr Dermatol. 2002;191:19-25.

9. Roncioletti F, Casciaro S, Boccaccio P, Rebora A. Annular pustular psoriasis and systemic lupus erythematosus. Int J Dermatol. 1990;294:290-2.

Notes

Source of Support: This article has no funding source.

Conflict of Interest: The authors have no conflict of interest to declare.

Copyright by authors of this article. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

Request permissions
If you wish to reuse any or all of this article please use the e-mail (contact@odermatol.com) to contact with publisher.

Related Content:

Related Articles Search Authors in

http://orcid.org/0000-0001-6330-2856
http://orcid.org/0000-0002-5942-441X
http://orcid.org/0000-0003-3455-3810

Rights and permissions

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

Comments are closed.