Sinus Histiocytosis (Rosai-Dorfman Disease) of the Suprasellar Region: MR Imaging Findings—A Case Report

Woodcock, Richard; Mandell, James W.; Lipper, Maurice H.

doi:10.1148/radiology.213.3.r99dc30808

Cited by 77 publications

(33 citation statements)

References 18 publications

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“…Although extranodal involvement is known to occur, isolated intracranial RDD is very rare. Out of 80 reported intracranial RDD cases, only 5 were in children [3][4][5][6][7][8].…”

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confidence: 99%

Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child: a case report and review of the literature

Gupta

Bagdi²,

Sunitha³

et al. 2011

BJR

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ABSTRACT. We report the first case of extensive involvement of isolated intracranial Rosai-Dorfman's disease (RDD) in a child. Our case is unique because it presents with involvement of the middle cranial fossa, cavernous sinus, pituitary gland, orbit, ethmoid and sphenoid sinuses. Previous cases of intracranial RDD in children have reported separate involvement of cavernous sinus, suprasellar region, and frontal and petroclival regions. Involvement of the pituitary gland has so far not been reported. A 14-year-old male presented with a medical history of loss of vision, raised erythrocyte sedimentation rate (ESR), and abnormal prolactin and cortisol levels. Radiologically the diagnosis was meningioma. The histopathological diagnosis was RDD with emperipolesis and S-100 positivity. RDD is a histiocytic proliferation of unknown aetiology, which commonly affects lymph nodes. Uncommonly it involves the extranodal sites and rarely the central nervous system (CNS). 80 cases of RDD involving CNS have been reported in the literature, and only 5 were in children. Although the definitive diagnosis of RDD disease is based on the histopathology report, it should be included in the differentials of a lesion mimicking meningioma especially in children.

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“…Although extranodal involvement is known to occur, isolated intracranial RDD is very rare. Out of 80 reported intracranial RDD cases, only 5 were in children [3][4][5][6][7][8].…”

mentioning

confidence: 99%

Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child: a case report and review of the literature

Gupta

Bagdi²,

Sunitha³

et al. 2011

BJR

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“…Rare cases with sellar lesions present with symptoms related to pituitary dysfunction and visual loss. 19,27) Previous intracranial RosaiDorfman disease cases most commonly revealed involvement of cervical lymph nodes (about half of cases), followed by the skeletal system, or salivary glands. 4,23) Most patients with Rosai-Dorfman disease follow a good clinical course; when the mass was surgically resected, the patients improved postoperatively.…”

Section: Discussionmentioning

confidence: 99%

Isolated Intracranial Rosai-Dorfman Disease Without Dural Attachment -Case Report-

Fukushima

Yachi

Ogino

et al. 2011

Neurol. Med. Chir.(Tokyo)

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A 33-year-old female presented with an isolated well-enhanced intracerebral lesion with peritumoral edema in the frontal lobe, which was tentatively diagnosed preoperatively as either a primary intraparenchymal neoplasm or metastatic brain tumor. However, histological examinations yielded a diagnosis of Rosai-Dorfman disease. Isolated intracranial Rosai-Dorfman disease is very rare, and without dural attachment, as in our case, is exceptional. The present case mimicked intraparenchymal neoplasm. Rosai-Dorfman disease should be considered in the differential diagnosis of isolated intraparenchymal tumors. Magnetic resonance imaging including diffusion-weighted imaging may be helpful in the diagnosis of isolated intracranial Rosai-Dorfman disease.

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“…Yachnis 10 presented case of 35 yr old man with bilateral contrast enhancing masses, consistent with meningiomas which on histopathology turned out as RDD and was confirmed by IHC. Wood rock and colleagues 11 reported RDD of suprasellar region in 15yr old girl, presenting as enlargement of pituitary infundibulum with extension into adjacent areas (suprasellar cistern, optic chiasma). Differential diagnosis included suprasellar germinoma, LCH and metastasis.…”

Section: Methodsmentioning

confidence: 99%

Rosai Dorfman Disease in CNS 19 Cases from one Institute

Bezwada¹

2016

jmscr

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Sinus Histiocytosis (Rosai-Dorfman Disease) of the Suprasellar Region: MR Imaging Findings—A Case Report

Cited by 77 publications

References 18 publications

Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child: a case report and review of the literature

Isolated intracranial Rosai-Dorfman disease mimicking meningioma in a child: a case report and review of the literature

Isolated Intracranial Rosai-Dorfman Disease Without Dural Attachment -Case Report-

Rosai Dorfman Disease in CNS 19 Cases from one Institute

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