Cutaneous Rosai-Dorfman disease: A separate clinical entity

• Príomhchruthaitheoirí: Tiffany Hinojosa (Údar), Elmira Ramos (Údar), Daniel J. Lewis (Údar), Laurent del Angel (Údar), Ramya Vangipuram (Údar), Andrew J. Peranteau (Údar), Stephen K. Tyring (Údar)
• Formáid: LEABHAR
• Foilsithe / Cruthaithe: Wolters Kluwer Medknow Publications, 2017-07-01T00:00:00Z.
• Ábhair: article
• Rochtain ar líne: Connect to this object online.

Rosai-Dorfman disease is a benign, self-limited non-Langerhans cell histiocytosis of unknown etiology. Its most common clinical feature is extraordinary massive painless cervical lymphadenopathy. This entity may be limited to the lymph nodes; however, more than 40% of patients have extranodal involv...