Cutaneous Rosai-Dorfman disease
DOI:
https://doi.org/10.29176/2590843X.1969Keywords:
Cutaneous Rosai-Dorfman disease, Emperipolesis, Sinus histiocytosis with massive lymphadenopathyAbstract
It is a rare and generally benign histiocytic proliferative disorder that mainly affects the cervical lymph nodes, however, it can have skin involvement in 10% of cases, it is associated with nonspecific systemic symptoms and symptoms in some paraclinical symptoms. A cutaneous form without symptoms or systemic commitment has been described, which is shown in this case. Its etiology is unknown, although several theories have been proposed. It typically involves the face and trunk, manifests as asymptomatic reddish-brown to yellow papules, plaques, or nodules. This entity has a chronic course, there is no specific treatment, it must be individualized according to the severity and extension of the lesions and in many cases clinical surveillance is proposed.
Author Biographies
Erika Patricia Muñoz-Herrera, Universidad de Antioquia, Medellín, Colombia.
Residente de Dermatología, Universidad de Antioquia, Medellín, Colombia.
Emil Jiménez-Berástegui, Universidad de Antioquia, Medellín, Colombia.
Residente de Patología, Universidad de Antioquia, Medellín, Colombia.
Juan David Ruiz-Restrepo, Universidad de Antioquia, Medellín, Colombia.
Patólogo, Fundación Colombiana de Cancerología Clínica Vida. Docente, Dermatopatología, Universidad de Antioquia, Medellín, Colombia.
References
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Copyright (c) 2024 Erika Patricia Muñoz-Herrera, Emil Jiménez-Berástegui, Juan David Ruiz-Restrepo
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