Isolated cerebral Rosai–Dorfman disease presenting as a sole mass protruding into the fourth ventricle: A case report

Friconnet, Guillaume; Duchesne, Mathilde; Gueye, Marcel; Caire, François; Mounayer, Charbel; Émile, Jean-François; Labrousse, François; Rouchaud, Aymeric

doi:10.1016/j.radcr.2021.04.021

Cited by 4 publications

(5 citation statements)

References 15 publications

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“…13,14 Friconnet et al reported a case of RDD in a 30-year-old man presenting as an isolated mass arising from the right cerebellar peduncle and protruding into the fourth ventricle. 15 Morandi et al, in 2000, reported the first case of isolated fourth ventricular RDD in a 22-year-old woman. 2 Patwardhan et al described the second case of isolated RDD in a 40-year-old man who presented as an enhancing lobulated mass expanding the atrium and the occipital horn of the lateral ventricle.…”

Section: Discussionmentioning

confidence: 99%

“…13 14 Friconnet et al reported a case of RDD in a 30-year-old man presenting as an isolated mass arising from the right cerebellar peduncle and protruding into the fourth ventricle. 15 Morandi et al, in 2000, reported the first case of isolated fourth ventricular RDD in a 22-year-old woman. 2…”

Section: Discussionmentioning

confidence: 99%

“…Radiological examination remains unable to establish the diagnosis by itself. 15 The lesion was excised by telovelar approach exposing well-circumscribed, gray-white nodular lesion (►Fig. 2).…”

Section: Discussionmentioning

confidence: 99%

“…Emperipolesis is the hallmark of RDD. 15 Immunoprofile reveals immunoreactivity of histiocytes for S100 and CD68, and negativity for CD1a (►Fig. 5).…”

Section: Discussionmentioning

confidence: 99%

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Fourth Ventricular Rosai–Dorfman Disease Mimicking Intraventricular Tumor in Young Adult: A Rare Case Report

Chougule,

Prabhakar,

Tadwalkar

et al. 2024

Asian J Neurosurg

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Rosai–Dorfman disease (RDD) or sinus histiocytosis with massive lymphadenopathy can present with or without systemic disease. It is a benign histioproliferative disorder characterized by generalized lymphadenopathy, weakness, anemia, and rarely extranodal involvement. While RDD most commonly affects lymph nodes, extranodal involvement of multiple organs has been reported, including the central nervous system (CNS). However, CNS involvement in RDD is rare and is not well characterized. Isolated involvement of the fourth ventricle is even rarer. Such lesions may be mistaken for intraventricular tumors such as ependymoma or medulloblastoma. This report highlights the necessity to consider RDD as a differential diagnosis in case of intraventricular space-occupying lesion.

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Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

Section: Discussionmentioning

confidence: 99%

“…Emperipolesis is the hallmark of RDD. 15 Immunoprofile reveals immunoreactivity of histiocytes for S100 and CD68, and negativity for CD1a (►Fig. 5).…”

Section: Discussionmentioning

confidence: 99%

See 2 more Smart Citations

Fourth Ventricular Rosai–Dorfman Disease Mimicking Intraventricular Tumor in Young Adult: A Rare Case Report

Chougule,

Prabhakar,

Tadwalkar

et al. 2024

Asian J Neurosurg

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“…Moreover, the occipital intraventricular lesion had been partially removed ( 16 ). Finally, a recent study has reported a 30-year-old man, a case of RDD presented as an isolated right cerebellar peduncle lesion bulging into the fourth ventricle ( 17 ).…”

Section: Discussionmentioning

confidence: 99%

Intracranial Rosai Dorfman Disease Presented With Multiple Huge Intraventricular Masses: A Case Report

et al. 2022

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IntroductionRosai-Dorfman disease (RDD) usually presents with painless cervical lymphadenopathy during the two first decades of life, with or without extranodal involvement. Exclusive extranodal manifestation, and especially central nervous system (CNS) involvement, is uncommon. The etiology remains unknown and definitive diagnosis is based on characteristic histopathological and immunohistochemical features showing S100(+) CD1a(−) RDD type histiocytes with emperipolesis. Most CNS cases are dural-based masses.Case PresentationHerein, we present a case of RDD in an 8-year-old boy, who presented with multiple huge intraventricular masses.ConclusionRegarding rare CNS involvement and lack of established evidence-based therapeutic approaches, reports of any individual case can supply further beneficial data concerning treatment approaches and long-term effectiveness of therapeutic strategies.

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A lesion of the patella: An unexpected location of Rosai-Dorfman disease: A case report

Sassi

M'rad²,

Kacem

et al. 2022

International Journal of Surgery Case Reports

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Isolated cerebral Rosai–Dorfman disease presenting as a sole mass protruding into the fourth ventricle: A case report

Cited by 4 publications

References 15 publications

Fourth Ventricular Rosai–Dorfman Disease Mimicking Intraventricular Tumor in Young Adult: A Rare Case Report

Fourth Ventricular Rosai–Dorfman Disease Mimicking Intraventricular Tumor in Young Adult: A Rare Case Report

Intracranial Rosai Dorfman Disease Presented With Multiple Huge Intraventricular Masses: A Case Report

A lesion of the patella: An unexpected location of Rosai-Dorfman disease: A case report

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