The Rosai-Dorfman Syndrome: A Case Report
Nadia Mebrouk *
Pediatric Unit P4, Children’s Hospital of Rabat, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
Najlae Attari
Pediatric Unit P4, Children’s Hospital of Rabat, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
Boutaina Halimi
Pediatric Unit P4, Children’s Hospital of Rabat, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
Loubna Chtouki
Pediatric Unit P4, Children’s Hospital of Rabat, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
Najat Lamalmi
Laboratory of Anatomy and Pathologic Cytology, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
Abdelali Bentahila
Pediatric Unit P4, Children’s Hospital of Rabat, CHU Ibn Sina, Mohamed V University, Rabat, Morocco.
*Author to whom correspondence should be addressed.
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.
Keywords: Rosai dorfman syndrome, child, immunosuppressants