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"Do Young Kim"

Case Report

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Rosai-Dorfman Disease in Thoracic Spine: A Rare Case of Compression Fracture
Korean J Spine. 2014;11(3):198-201.   Published online September 30, 2014
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Rosai-Dorfman Disease in Thoracic Spine: A Rare Case of Compression Fracture
Korean J Spine. 2014;11(3):198-201.   Published online September 30, 2014
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Sinus histiocytosis with massive lymphadenopathy known as Rosai-Dorfman disease is characterized by painless bilateral cervical lymphadenopathy. Extranodal manifestations are uncommon and spinal involvement is rare. A 15-year-old man presented with intermittent midthoracic back pain only. He had no specific findings on neurologic examinations, hematologic and biochemical laboratory tests. Radiological examination of thoracic spine revealed collapse of T6 vertebrae with thoracic kyphosis and osteolytic lesion of T12 vertebra body. He underwent a removal of bone tumor, anterior reconstruction with mesh and pedicle screw fixation via posterior approach for pathologic confirmation and stabilization. Histopathologic study of the lesion revealed focal infiltration of large histiocytes showing emperipolesis. Immunochemistry stain of histiocytes was positive for CD68 and S-100 but negative for CD1a. This report presents a rare case and literature review of extranodal Rosai-dorfman disease in thoracic spine.

Citations

Citations to this article as recorded by  Crossref logo
  • Diagnosis and Management of Extranodal Rosai-Dorfman Disease Isolated to the Thoracic Spine: Systematic Review and Illustrative Case
    Rithvik Ramesh, Robert C. Osorio, Melike Pekmezci, Lauren Boreta, Debajyoti Datta, Nima Alan
    World Neurosurgery.2026; 212: 125082.     CrossRef
  • Isolated Rosai-Dorfman disease of the spine: A systematic literature review
    Maroua Slouma, Sirine Bouzid, Karima Tlili, Dahmani Yedaes, Khaled Radhwen, Imen Gharsallah
    Clinical Neurology and Neurosurgery.2024; 239: 108206.     CrossRef
  • Diagnosis and treatment of Rosai-Dorfman disease of the spine: a systematic literature review
    Pan-pan Hu, Feng Wei, Xiao-guang Liu, Zhong-jun Liu
    Systematic Reviews.2021;[Epub]     CrossRef
  • Primary Rosai‑Dorfman disease of bone arising in the infantile ilium: A case report
    Yuya Izubuchi, Koji Suzuki, Yoshiaki Imamura, Hajime Katayama, Yusei Ohshima, Akihiko Matsumine
    Experimental and Therapeutic Medicine.2020;[Epub]     CrossRef
  • Long-Term Outcome of Spinal Extranodal Rosai-Dorfman Disease: A Report of Two Cases and Systematic Review
    Saleh S. Baeesa, Hani Mahboob, Yazid Maghrabi, Mohammad Binmahfoodh, Jaudah Almaghrabi
    World Neurosurgery.2020; 144: 1.     CrossRef
  • Nonresectable Thoracic Rosai-Dorfman Disease: A Case Report and Review of the Literature
    Cheng-Kai Lin, Yu-Duan Tsai
    World Neurosurgery.2019; 132: 309.     CrossRef
  • An Institutional Review of Tuberculosis Spine Mimics on MR Imaging: Cases of Mistaken Identity
    SunithaPalasamudram Kumaran, PushpaBhari Thippeswamy, BhavanaNagabhushan Reddy, Sankar Neelakantan, Sanjaya Viswamitra
    Neurology India.2019; 67(6): 1408.     CrossRef
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Radiologic Adjacent Segment Degeneration and Clinical Outcome after Two Level Fusion (L3-4-5 and L4-5-S1) in Degenerative Lumbar Spinal Disease.
Korean J Spine. 2010;7(3):143-149.
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Radiologic Adjacent Segment Degeneration and Clinical Outcome after Two Level Fusion (L3-4-5 and L4-5-S1) in Degenerative Lumbar Spinal Disease.
Korean J Spine. 2010;7(3):143-149.
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OBJECTIVE
We retrospectively analyzed correlation of the development of radiologic adjacent segment degeneration (ASD), clinical outcome, and the vertebral level of fusion in two-level posterior lumbar fusion cases. Furthermore, risk factors of ASD were investigated.
METHODS
From 2000 to 2007, a total of 50 patients were evaluated. Their mean age was 55.0 years and mean follow-up period was 52.7 months. The patients were divided into two groups according to the vertebral level of the fused segment. Group I included 35 patients with L3-4-5 fusion, while 15 patients with L4-5-S1 fusion were categorized into group II. The patients were also divided into two groups, according to the development of ASD. Odom's criteria was used to study clinical outcome, and Cobb's angle was used to evaluate radiologic outcome RESULTS: Of 50 patients, radiologic ASD was found in 24 (48.0%) patients. Group I showed 16 (45.7%) patients with ASD, while Group II showed 8 (53.3%) patients with ASD, and they did not show a significant difference in development of ASD and clinical outcome. Clinical outcome of patients with ASD and the ones without ASD did not show significant difference. Meanwhile, patients with ASD were older and showed decrease of the lordotic angle, as well as significant hypermobility in the cranial adjacent segment, during follow-up.
CONCLUSION
Different vertebral regions of fusion in two-level posterior lumbar fusion did not show significant difference in development of radiologic ASD and clinical outcome. In the development of ASD, decrease of the lordotic angle, hypermobility in the cranial adjacent segment and age were significant factors.
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  • 37 Download