Intracranial Rosai–Dorfman disease: Case report and literature review

Deng, Xin; Xie, Xuebin; Ye, Yu-qing; Liao, Ting Kai

doi:10.1016/j.ejrex.2010.09.005

European Journal of Radiology Extra

2010

DOI: 10.1016/j.ejrex.2010.09.005

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Intracranial Rosai–Dorfman disease: Case report and literature review

Xin Deng

Xuebin Xie

Yu-qing Ye

et al.

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Cited by 4 publications

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“…210,[212][213][214][215][217][218][219][220][221] Central nervous system involvement in 287 cases of Rosai-Dorfman disease. [1-5,7,9,10,12-24,26-39,41,44-48,50-54,56-68,70,72-96,98,99,102-111,113-115,117-123,126- 129,130,132-135,137-142,144,146-148,150-154,157-161,163-175,177,178,181-185,187-191,193-196,198,200,202-210,212-215,217-221] …”

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

Tatit

Raffa²,

Motta

et al. 2021

Surgical Neurology International

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Background: Rosai-Dorfman disease (RDD) is a rare non-Langerhans cell histiocytic proliferative disorder classically as a massive cervical lymphadenopathy. However, over the years, extranodal locations were confirmed with the central nervous system involvement in less than 5% of cases, which is marked as a significant differential diagnosis of meningiomas, with which they are widely confused due to the similarity of their radiological images. Case Description: We report a 37-year-old man and 45-year-old man who were diagnosed with intracranial RDD but whose radiological images mimic meningiomas, requiring anatomopathological and tumor’s immunohistochemistry for definitive diagnosis. Moreover, a review of 184 publications with 285 cases of intracranial involvement of this disease was also performed, comparing these findings with those brought in the previous studies. Conclusion: Intracranial Rosai-Dorfman tumors should always be remembered as differential diagnosis of meningiomas since they are similar radiologically and macroscopically. Once remembered and diagnosed, the lesion must be treated following the same pattern of resection done in meningiomas and, treatment’s differences will not occur in the surgical excision technique, but in complementary chemotherapy implementation, radiotherapy, and even with radiosurgery aid, depending on the case. Thus, it is possible to obtain better results than with just the isolated surgical procedure.

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mentioning

confidence: 99%

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

Tatit

Raffa²,

Motta

et al. 2021

Surgical Neurology International

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Rosai-Dorfman disease with spinal and multiple intracranial involvement: a case report and literature review

Qin

Lan

et al. 2019

British Journal of Neurosurgery

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Rosai-Dorfman Disease of the Central Nervous System

et al. 2014

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Rosai-Dorfman disease (RDD), also known as sinus histiocytosis with massive lymphadenopathy (SHML), is an uncommon benign idiopathic lymphoproliferative disorder. The histologic hallmark of RDD is the finding of emperipolesis displayed by lesional histiocytes. 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. As a result, therapeutic approaches to CNS involvement in RDD are not well established. Herein we report 6 cases of RDD with isolated CNS involvement and review the literature on RDD with CNS involvement. One of the presented cases exhibited intramedullary involvement of the spinal cord—a very rare form of RDD with CNS involvement.

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Intracranial Rosai–Dorfman disease: Case report and literature review

Cited by 4 publications

References 18 publications

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

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

Rosai-Dorfman disease with spinal and multiple intracranial involvement: a case report and literature review

Rosai-Dorfman Disease of the Central Nervous System

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