Rosai-dorfman disease: Cutaneous and parotid involvement
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Lippincott Williams and Wilkins
Abstract
Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy, is a rare and benign proliferative disease that affects histiocytes. Its etiology remains unclear. Rosai-Dorfman disease primarily affects lymph nodes with many extranodal manifestations present, including cutaneous, pulmonary, ophthalmic, and gastrointestinal. Diagnosis is mainly histologic with the presence of Rosai-Dorfman cells, which demonstrate emperipolesis. We report a case of a 30-year-old man who presented with a facial cutaneous mass and was diagnosed with RDD; he underwent surgical excision. The patient experienced recurrent lesions on the surgical scar and parotid gland as well as the lower back. Treatment consisted of systemic steroids and surgical excision. © Copyright 2019 Wolters Kluwer Health, Inc. All rights reserved.
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Keywords
Cutaneous rosai-dorfman, Parotid gland, Rosai-dorfman disease, Sinus histiocytosis with massive lymphadenopathy, Adrenal cortex hormones, Adult, Follow-up studies, Histiocytosis, sinus, Humans, Lymph node excision, Lymphadenopathy, Male, Positron-emission tomography, Rare diseases, Recurrence, Risk assessment, Severity of illness index, Skin, Treatment outcome, Corticosteroid, Case report, Diagnostic imaging, Follow up, Human, Lymph node dissection, Pathology, Positron emission tomography, Procedures, Rare disease, Recurrent disease, Sinus histiocytosis