Surgical management and outcome of primary intracranial Rosai-Dorfman disease: a single-institute experience and pooled analysis of individual patient data

Zhang, Guijun; Ma, Xuanlong; Zhang, Yaping; Liang, Hao; Wang, Liang; Zhang, Junting; Wu, Zhen; Li, Da

doi:10.1007/s10143-023-01983-9

Cited by 2 publications

(1 citation statement)

References 44 publications

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“…In general, observation is appropriate for patients with uncomplicated lymphadenopathy and asymptomatic cutaneous lesions. Surgical excision is often curative for patients with solitary extranodal disease ( 30 ). Systemic therapies are typically employed for multifocal or treatment-resistant cases ( 11 , 31 ).…”

Section: Discussionmentioning

confidence: 99%

Case report: A rare case of isolated sigmoid Rosai-Dorfman disease on contrast-enhanced CT and 18F-FDG PET/CT

Qi,

Luo,

Shao

et al. 2024

Front. Med.

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Rosai-Dorfman disease (RDD) is an uncommon histiocytic disorder that occurs in nodal and/or extranodal sites. Extranodal RDD exhibits a wide range of clinical and radiological presentations, frequently leading to misdiagnoses. Involvement of the gastrointestinal (GI) system is uncommon, accounting for less than 1% of the reported cases. Here we present a case of a 54-year-old male who complained of abdominal distention and was diagnosed with RDD affecting the sigmoid colon, manifesting as a sigmoid mass. The patient had a past medical history of liver transplantation due to hepatocellular carcinoma (HC). This report details the multiphase contrast-enhanced computed tomography (CT) and fluorodeoxyglucose (18F-FDG) positron emission tomography (PET-CT) imaging findings of RDD involving the sigmoid colon without lymphadenopathy, and a review of the relevant literature is provided.

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Section: Discussionmentioning

confidence: 99%

Case report: A rare case of isolated sigmoid Rosai-Dorfman disease on contrast-enhanced CT and 18F-FDG PET/CT

Qi,

Luo,

Shao

et al. 2024

Front. Med.

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Radiotherapy and stereotactic radiotherapy for multifocal intracranial and intramedullary Rosai–Dorfman disease

D'Oria,

Rossitto,

Giraldi

et al. 2024

Clinical & Exp Neuroim

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BackgroundWe present a case of a 51‐year‐old man affected by Rosai–Dorfman disease with multiple disseminated intraparenchymal and a single spinal cord localization, presenting with dysphasia and paraparesis.Case PresentationThe patient elected to receive medical steroidal therapy and two radiotherapy cycles. Steroids allowed initial regression of some lesions, while radiotherapy constituted an optimal maintenance treatment. At 6‐year follow up, the patient did not develop any new neurological damage in respect to baseline.ConclusionsAdjuvant therapy with radiotherapy and steroidal therapy is a valid option in multicentric Rosai–Dorfman disease patients not eligible for surgery.

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Surgical management and outcome of primary intracranial Rosai-Dorfman disease: a single-institute experience and pooled analysis of individual patient data

Cited by 2 publications

References 44 publications

Case report: A rare case of isolated sigmoid Rosai-Dorfman disease on contrast-enhanced CT and 18F-FDG PET/CT

Case report: A rare case of isolated sigmoid Rosai-Dorfman disease on contrast-enhanced CT and 18F-FDG PET/CT

Radiotherapy and stereotactic radiotherapy for multifocal intracranial and intramedullary Rosai–Dorfman disease

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