Rosai-Dorfman Disease (RDD) With Isolated Compromise of the Central Nervous System. Case Report and Literature Review

Authors

  • Daniel Ruiz Pardo Escuela Colombiana de Medicina, Universidad El Bosque. Bogotá
  • Octavio de Jesús Arévalo Espejo Universidad de Texas, Houston, UT Health Science Health Center McGovern Medical School.
  • Leomar Y. Ballester Universidad de Texas, Houston, UT Health Science Health Center McGovern Medical School.
  • Roy Francisco Riascos-Castaneda Universidad de Texas, Houston, UT Health Science Health Center McGovern Medical School.

Keywords:

Histiocytosis, sinus, Central nervous system, Tomography X-ray computed

Abstract

Rosai-Dorfman Disease (RDD) or Sinus Histiocytosis with Massive Lymphadenopathy (SHML) is a rare benign histiocytic disorder, usually affecting the lymph nodes. Intracranial involvement is an uncommon variant of the disease; however, intracranial lesions without concomitant nodular involvement is exceptional. The lack of brain imaging patterns can lead to surgery due to misdiagnosis, with causes attributed to a probable malignant origin. Histopathological diagnosis is usually made after the surgical procedure. There is no consensus related to diagnosis, clinical course and treatment of this disease. A case report is presented on isolated intracranial RDD, with a retrospective reading of the imaging studies. typical

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References

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Published

2019-03-30

How to Cite

(1)
Ruiz Pardo, D. .; Arévalo Espejo, O. de J. .; Y. Ballester, L. .; Riascos-Castaneda, R. F. . Rosai-Dorfman Disease (RDD) With Isolated Compromise of the Central Nervous System. Case Report and Literature Review. Rev. colomb. radiol. 2019, 30, 5094-5097.

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Section

Case reports
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