» Articles » PMID: 26915894

MRI and CT Findings of Isolated Intracranial Rosai-Dorfman Disease in a Child

Overview
Journal Neuroradiol J
Publisher Sage Publications
Specialties Neurology
Radiology
Date 2016 Feb 27
PMID 26915894
Citations 7
Authors
Affiliations
Soon will be listed here.
Abstract

Isolated intracranial Rosai-Dorfman disease (RDD) is extremely rare in pediatric patients. We present the case of a 22-month-old boy whom had isolated intracranial RDD involvement. To our knowledge, a parieto-occipital regional involvement without a dural tail sign has not been previously documented. Also, the mass contained hyperintense central T1 foci, and hypointense T2 and gradient echo foci; which are helpful in the differential diagnosis from meningioma. The magnetic resonance and computed tomography imaging findings are discussed and the follow-up course is presented in this paper.

Citing Articles

Case report: A rare case of isolated sigmoid Rosai-Dorfman disease on contrast-enhanced CT and F-FDG PET/CT.

Qi W, Luo Z, Shao M, Chen M, Liao F, Hu L Front Med (Lausanne). 2024; 11:1425112.

PMID: 38938381 PMC: 11210213. DOI: 10.3389/fmed.2024.1425112.


Bifocal Intracanial Rosai-Dorfman Disease Mimicking Lymphoplasmacyte-Rich Meningioma: Diagnostic Pitfalls About a Case Report.

El Ouazzani H, Touarsa F, Houssaini Z, Hakkou M, Elouadghiri M, Ouhabi A Clin Med Insights Case Rep. 2023; 16:11795476231172354.

PMID: 37197032 PMC: 10184201. DOI: 10.1177/11795476231172354.


Staging surgery for intraventricular bilateral giant Rosai-Dorfman disease in children.

Zhang J, Li D, Cheng R, Zhang N, Ni X, Ge M Pediatr Investig. 2022; 6(1):50-54.

PMID: 35382423 PMC: 8960918. DOI: 10.1002/ped4.12306.


Steroid responsive cavernous sinus syndrome due to Rosai-Dorfman disease: beyond Tolosa-Hunt syndrome - a case report.

Nobrega P, Rodrigues P, Pereira I, de Figueiredo Santos C, Gerson G, de Arruda J BMC Neurol. 2021; 21(1):264.

PMID: 34225703 PMC: 8256567. DOI: 10.1186/s12883-021-02255-z.


Rosai-Dorfman disease mimicking images of meningiomas: Two case reports and literature review.

Tatit R, Raffa P, de Almeida Motta G, Bocchi A, Guimaraes J, Franceschini P Surg Neurol Int. 2021; 12:292.

PMID: 34221623 PMC: 8247728. DOI: 10.25259/SNI_918_2020.


References
1.
Lungren M, Petrella J, Cummings T, Grant G . Isolated intracranial Rosai-Dorfman disease in a child. AJNR Am J Neuroradiol. 2009; 30(10):E148-9. PMC: 7051273. DOI: 10.3174/ajnr.A1812. View

2.
Ludemann W, Banan R, Samii A, Koutzoglou M, Di Rocco C . Cerebral Rosai-Dorfman disease. Childs Nerv Syst. 2015; 31(4):529-32. DOI: 10.1007/s00381-015-2629-2. View

3.
Gupta K, Bagdi N, Sunitha P, Ghosal N . Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child: a case report and review of the literature. Br J Radiol. 2011; 84(1003):e138-41. PMC: 3473498. DOI: 10.1259/bjr/15772106. View

4.
Varan A, Sen H, Akalan N, Oguz K, Saglam A, Akyuz C . Pontine Rosai-Dorfman disease in a child. Childs Nerv Syst. 2015; 31(6):971-5. DOI: 10.1007/s00381-015-2632-7. View

5.
Rosai J, DORFMAN R . Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity. Arch Pathol. 1969; 87(1):63-70. View