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May 31, 2026World Neurosurgery0 citationsOpen Access

Diagnosis and Management of Extranodal Rosai-Dorfman Disease Isolated to the Thoracic Spine: Systematic Review and Illustrative Case

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RRRithvik RameshRORobert C. OsorioMPMelike Pekmezci

Key Points

  • This research aims to enhance understanding of the diagnosis and treatment of extranodal Rosai-Dorfman Disease in the thoracic spine.
  • A systematic review of published cases of extranodal RDD isolated to the thoracic spine was conducted.
  • Patient demographics, clinical presentation, imaging, histopathologic findings, treatments, and outcomes were analyzed.
  • An illustrative case of a patient with thoracic spinal RDD was also reported.
  • The illustrative case involved a 21-year-old woman with T3 spinal cord compression, confirmed as RDD.
  • Recurrence occurred post-surgery in 21% of reviewed cases, despite treatment, indicating a challenging prognosis.
  • All patients demonstrated clinical improvement at last follow-up, underscoring the effectiveness of multimodal treatment approaches.

Abstract

ABSTRACT Background Rosai-Dorfman Disease (RDD) is a rare histiocytic disorder typically affecting lymph nodes. Extranodal RDD is uncommon, and isolated central nervous system (CNS) or spinal disease is particularly rare, limiting guidance on diagnosis and management. Methods We report a patient treated at our institution and conducted a systematic review of all published cases of extranodal RDD isolated to the thoracic spine. Patient demographics, clinical presentation, imaging and histopathologic findings, treatments, and outcomes were extracted. Results A 21-year-old woman presented with progressive back pain and bilateral lower extremity paresthesia. MRI revealed an enhancing extradural lesion at T3 causing spinal cord compression. Surgical resection confirmed RDD. Despite postoperative steroids and radiotherapy, recurrence occurred within months, necessitating repeat surgery. Subsequent imaging revealed further progression with unresectable extension. She was treated with corticosteroids and cobimetinib, resulting in gradual radiographic and symptomatic improvement. Our review identified 41 cases of thoracic spinal RDD, including this case. Most patients were male (80%) with median age of 40 years. Common symptoms included lower extremity weakness (83%) and sensory deficits (64%). Lesions were typically T1 isointense and contrast-enhancing. Histopathology consistently showed S100+ and CD68+ histiocytes with emperipolesis. Surgical resection was the primary treatment (98%). Despite recurrence in 21% of cases, all patients showed clinical improvement at last follow-up. Conclusions Thoracic spinal RDD is a rare and diagnostically challenging entity requiring multimodal treatment. Surgical decompression remains the mainstay of therapy for cord compression, while adjunctive medical treatments—including corticosteroids, radiation, and targeted agents—may be necessary for long-term disease control.

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Cite This Study

Ramesh et al. (2026) studied this question.

synapsesocial.com/papers/6a1bcfe15783ba022b6fbc25https://doi.org/10.1016/j.wneu.2026.125082
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Also Consider

Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context:

  1. 1ISOLATED CERVICAL INTRADURAL ROSAI-DORFMAN'S DISEASE – A VERY RARE ENTITY2024
  2. 2Postoperative Radiotherapy in Spinal Rosai-Dorfman Disease: A Case Report and Literature Review2025
  3. 3Spinal Rosai-Dorfman Disease with Isolated Severe Neuropathic Pain: A Case Report2024
  4. 4Localized Rosai-Dorfman disease: Case report of an uncommon tumor and a brief review of the literature2025
  5. 5Isolated spinal Rosai–Dorfman disease with secondary hypertrophic pachymeningitis: A case report with 20-year follow-up, highlighting rapid recurrence and <i>de novo</i> lesion formation2026