Extranodal Rosai-Dorfman: a rare disease with a common clinical manifestation.

Authors

  • María Carolina Fragozo-Ramos Servicio de Medicina Interna. ESE Hospital Universitario del Caribe. Universidad de Cartagena. Cartagena. Colombia https://orcid.org/0000-0002-6657-9989
  • Paola Andrea Ortiz-Marin Servicio de Medicina Interna. ESE Hospital Universitario del Caribe. Universidad de Cartagena. Cartagena. Colombia
  • Marbel Karina Corzo-Pacheco Servicio de Patología. ESE Hospital Universitario del Caribe. Universidad de Cartagena. Cartagena. Colombia
  • Cesar Redondo-Bermudez Servicio de Patología. ESE Hospital Universitario del Caribe. Universidad de Cartagena. Cartagena. Colombia

DOI:

https://doi.org/10.32818/reccmi.a5n2a6

Keywords:

Rosai-Dorfman disease, bone, central nervous system, sinus histiocytosis, non-Langerhans cell histiocytosis.

Abstract

Sinusoidal histiocytosis with massive lymphadenopathy or Rosai-Dorfman disease (RDD) is a benign proliferative disorder of histiocytes. It is most frequently seen in children and young adults but can occur at any age. The disease is more common in men and individuals of African descent. It is an uncommon entity with a variety of clinical manifestations. We present a case of extranodal RDD of complex diagnosis with bone involvement and the central nervous system. In this case, the biopsy was conclusive highlighting the distinctive aspects of this pathology

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References

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Published

2020-08-31

How to Cite

1.
Fragozo-Ramos MC, Ortiz-Marin PA, Corzo-Pacheco MK, Redondo-Bermudez C. Extranodal Rosai-Dorfman: a rare disease with a common clinical manifestation. Rev Esp Casos Clin Med Intern [Internet]. 2020 Aug. 31 [cited 2024 Nov. 23];5(2):71-3. Available from: https://www.reccmi.com/RECCMI/article/view/503