The Rosai-Dorfman Syndrome: A Case Report

Mebrouk, Nadia and Attari, Najlae and Halimi, Boutaina and Chtouki, Loubna and Lamalmi, Najat and Bentahila, Abdelali (2023) The Rosai-Dorfman Syndrome: A Case Report. Asian Journal of Pediatric Research, 12 (2). pp. 9-12. ISSN 2582-2950

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Abstract

Sinus histiocytosis, also known as Rosaï Dorfman Syndrome (SRD), is a noncancerous condition that causes the growth of large masses of histiocytes in lymph nodes, primarily in the cervical area. Visceral damage is common, and diagnosis is made through histological examination. The cause of SRD is unknown and can occur at any age, even in children. The condition can sometimes improve spontaneously, but large tumor masses can cause compression and damage, particularly if they involve the retro-orbital or epidural areas. In most cases, it is best to avoid treatment, but therapeutic interventions may be necessary for forms of the disease that pose a direct threat or are progressing. Treatment is not standardized and may involve surgery, corticosteroids, immunosuppressants, and/or alpha interferon, depending on the individual case.

We present a case study of a 4-year-old child who had multiple bilateral adenopathies. The diagnosis was verified through a biopsy of the lymph nodes.

Item Type: Article
Subjects: AP Academic Press > Medical Science
Depositing User: Unnamed user with email support@apacademicpress.com
Date Deposited: 21 Apr 2023 09:55
Last Modified: 24 Sep 2024 11:05
URI: http://info.openarchivespress.com/id/eprint/1043

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