Please use this identifier to cite or link to this item: https://scidar.kg.ac.rs/handle/123456789/9110
Title: Rosai–Dorfman disease of vertebra: Case report and literature review
Authors: Igrutinovic, Zoran
Medovic R.
Markovic, Slavica
Kostic, Gordana
Raskovic Z.
Tanaskovic-Nestorovic J.
Radovanović M.
Vuletić B.
Issue Date: 2016
Abstract: © 2017, Turkish Journal of Pediatrics. All rights reserved. Rosai–Dorfman disease is a rare benign histiocytic disorder that arises predominantly in lymph nodes with fever and malaise, but can affect various organs, with or without lymphadenopathy. Solitary extranodal skeletal lesions are extremely rare. Herein, we describe a case of isolated disease of thoracic spine, with vertebral body fracture. A 14-year-old girl presented with cervical back pain for about one month as the only symptom. There was no lymphadenopathy. Results of laboratory tests were within reference ranges. The radiological examinations revealed collapse, osteolytic lesion and compressive fracture, which reduced vertical diameter of C4 vertebral body. The patient made a complete recovery after a limited C4 laminectomy, spondylodesis C3/C5 vertebra and biopsy of the lesion. Histologically, nonspecific cellular milieu and atypical histiocytic proliferation with emperipolesis, with CD68 and S100 positivity, confirmed a diagnosis of Rosai–Dorfman disease. Isolated extranodal skeletal Rosai–Dorfman disease should be considered among the differential diagnoses of similar changes, such as Langerhans cell histiocytosis, Erdheim–Cheister disease, eosinophilic granuloma, osteomyelitis, metastasis and lymphoma.
URI: https://scidar.kg.ac.rs/handle/123456789/9110
Type: review
DOI: 10.24953/turkjped.2016.05.020
ISSN: 0041-4301
SCOPUS: 2-s2.0-85020422542
Appears in Collections:Faculty of Medical Sciences, Kragujevac

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