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eISSN: 2581-9615 || CODEN: WJARAI || Impact Factor 8.2 ||  CrossRef DOI

Research and review articles are invited for publication in March 2026 (Volume 29, Issue 3) Submit manuscript

Lichenoid Sarcoidosis: A rare form of cutaneous sarcoidosis

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  • Lichenoid Sarcoidosis: A rare form of cutaneous sarcoidosis

Sophia abdel-ilah *, Maryem Aboudourib, Layla Bendaoud, Ouafa Hocar and Said Amal

Department of Dermatology, University hospital Mohammed VI of Marrakech, Morocco Bioscience and health laboratory, faculty of medicine and pharmacy, Cadi Ayyad University, Marrakech, Morocco.

Case Report

World Journal of Advanced Research and Reviews, 2025, 26(02), 3835-3837

Article DOI: 10.30574/wjarr.2025.26.2.2112

DOI url: https://doi.org/10.30574/wjarr.2025.26.2.2112

Received on 20 April 2025; revised on 25 May 2025; accepted on 27 May 2025

Background: Sarcoidosis, also known as Besnier-Boeck-Schaumann disease, is a systemic granulomatous disease of unknown origin that can affect various organs. Cutaneous manifestations are diverse, presenting initially in 80% of cases and being the sole sign of the disease in 25% of patients. Among these manifestations, lichenoid sarcoidosis is a rare form, accounting for only 1 to 2% of cutaneous cases. First described in 1899, it manifests as slightly scaly papules, primarily located on the trunk and face. Although often benign, this form can be associated with ocular and joint complications, especially in children. This article presents a case of lichenoid sarcoidosis in a 44-year-old woman.

Methods: we present the case of A 44-year-old woman presented with asymptomatic skin lesions on the trunk and face, evolving over three months. Clinical examination revealed flesh-colored papules grouped on the face, neck, and back. 

Results: Histological analysis showed non-caseating epithelioid granulomas. Laboratory tests were normal except for elevated ACE levels. Based on clinical and histological findings, a diagnosis of lichenoid sarcoidosis was made, and treatment with hydroxychloroquine and topical corticosteroids was initiated.

Discussion: Sarcoidosis is a multisystemic disease of unknown etiology, primarily affecting young adults, with a female predominance. Cutaneous manifestations, present in 20–25% of cases, may be nonspecific (such as erythema nodosum) or specific, featuring non-caseating granulomas. The lichenoid form, first described in 1899, presents as slightly scaly papules, mainly on the trunk and face. Though often benign, it may be associated with ocular and joint complications, particularly in children. In this case, the patient had no pulmonary or ocular involvement, and histological analysis confirmed the characteristics of lichenoid sarcoidosis. The main differential diagnoses include lichen scrofulosorum and other lichenoid dermatoses.

Conclusion: This article reports a case of lichenoid sarcoidosis in a woman, illustrating this rare form of cutaneous sarcoidosis, diagnosed based on clinical observation and histopathological analysis. 

Sarcoidosis; Lichenoid Sarcoidosis; Granulomas; Besnier-Boeck-Schaumann disease

https://wjarr.com/sites/default/files/fulltext_pdf/WJARR-2025-2112.pdf

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Sophia abdel-ilah, Maryem Aboudourib, Layla Bendaoud, Ouafa Hocar and Said Amal. Lichenoid Sarcoidosis: A rare form of cutaneous sarcoidosis. World Journal of Advanced Research and Reviews, 2025, 26(2), 3835-3837. Article DOI: https://doi.org/10.30574/wjarr.2025.26.2.2112

Copyright © Author(s). All rights reserved. This article is published under the terms of the Creative Commons Attribution 4.0 International License (CC BY 4.0), which permits use, sharing, adaptation, distribution, and reproduction in any medium or format, as long as appropriate credit is given to the original author(s) and source, a link to the license is provided, and any changes made are indicated.


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