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"Jong Eon Lee"

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"Jong Eon Lee"

Case Reports
Syringomyelia Coexisting With Guillain-Barre Syndrome
Hee-Sang Kim, Dong Hwan Yun, Jinmann Chon, Jong Eon Lee, Min Ho Park, Yoo Jin Han
Ann Rehabil Med 2013;37(5):745-749.   Published online October 29, 2013
DOI: https://doi.org/10.5535/arm.2013.37.5.745

Guillain-Barre syndrome (GBS) and syringomyelia are diseases of different entities. GBS is an acute post-infectious autoimmune disease which is mediated by autoantibodies against the myelin of peripheral nerves. Syringomyelia is a chronic disease characterized by a cavity extending longitudinally inside the spinal cord. A 67-year-old man is being hospitalized due to severe numbness and ascending weakness in all limbs. On neurological examination, the motor power of all limbs are decreased and show absence of deep tendon reflexes (DTRs). The patient is being diagnosed with GBS on the basis of the acute clinical course, nerve conduction studies of segmental demyelinating polyneuropathy, and a finding of albuminocytologic dissociation in the cerebrospinal fluid. The patient is presented with a new set of symptoms thereafter, which composes of sensory changes in the upper extremities, the urinary dysfunction including frequency and residual urine, spastic bilateral lower extremities, and increased reflexes of the knee and the biceps at follow-up examinations. The spinal magnetic resonance imaging in the sagittal section revealed a syrinx cavity between the fifth cervical and the first thoracic vertebral segment in the cord. The somatosensory evoked potential show sensory pathway defects between both the brachial plexus and the brain stem. Thus, this patient is being diagnosed with both GBS and syringomyelia. We report a case of symptomatic syringomyelia coexisting with GBS. Since the GBS is presented with a progressive muscle weakness and reduced DTRs, the muscle weakness and stiffness in the extremities suggests a concurrent syringomyelia might be easily overlooked.

Citations

Citations to this article as recorded by  
  • HIDROSSIRINGOMIELIA ASSOCIADA A NEUROSSÍFILIS EM PACIENTE COM HIV: RELATO DE CASO E REVISÃO SISTEMÁTICA
    Beatriz Ballarin Costa, Victor Mourão Vilela Barbosa, Waleriano Ferreira de Freitas, Antonio Pedro de Melo Moreira Suarte, Marcos Affonso Ballarin Costa, Jaime Garcia Pereira Neto
    Revista Contemporânea.2026; 6(1): e10129.     CrossRef
  • Uncommon concurrence of Guillain-Barré syndrome and cervical myelopathy in a paediatric patient: diagnostic challenge and clinical implications
    Nikita Diwan, Devina Singh, Chandra Kanta Kumar, Yashwant Kumar Rao
    BMJ Case Reports.2025; 18(8): e266822.     CrossRef
  • Comorbid presentation of syringomyelia and Guillain-Barre syndrome, attributed to mycoplasma, in a 6-year-old female patient
    Olga Vampertzi, Efterpi Dalpa, Theofanis Vavilis, Despoina Tramma
    BMJ Case Reports.2018; 2018: bcr-2018-225750.     CrossRef
  • 10,511 View
  • 26 Download
  • 3 Crossref
Spinal Cord Injury due to the Giant Cell Tumor of the Second Thoracic Vertebra: A Case Report
Hee-Sang Kim, Jong Eon Lee, Sang Soo Jung, Jinmann Chon, Dong Hwan Yoon, Yong-Koo Park, Eun Hye Cho
Ann Rehabil Med 2013;37(2):269-273.   Published online April 30, 2013
DOI: https://doi.org/10.5535/arm.2013.37.2.269

Giant cell tumor (GCT) is a relatively rare neoplasm. In GCT, the bone affection of the axial skeleton is extremely rare. Most GCT arises in the meta-epiphyseal ends of the long bones. Its peak incidence is between 30 to 40 years of age. GCT is usually classified as benign, but shows locally aggressive behavior and may occasionally undergo a malignant transformation. The patients with GCT in the spine often complain of the lower back pains, as the tumors primarily involve the sacrum. We report a case of an adolescent female complaining of the upper back pain with a sudden weakness of the lower extremities, later diagnosed with the GCT of the T2 vertebra. The present patient showed American Spinal Injury Association Impairment Scale (AIS) D before the surgery, which changed to AIS E after the treatments including the surgery, radiation therapy and rehabilitation.

Citations

Citations to this article as recorded by  
  • A rare pediatric case of thoracic spine giant cell tumor: Clinical implications and surgical strategies
    Ibrahim Fathallah, Ayham Qatza, Ahmed Al-Talep, Abd Alrhman Alajrd, Mohammad Alfattal, Ahmad Alhamoud
    International Journal of Surgery Case Reports.2025; 127: 110890.     CrossRef
  • Recurrent giant cell tumour of the thoracic spine managed by total en bloc spondylectomy and denosumab therapy: a case report
    Ping-Guo Duan, Yong-Hong Sheng, Chang-Hao Deng, Ben-Yu Tang, Hao-Qun Yao
    BMC Musculoskeletal Disorders.2020;[Epub]     CrossRef
  • Obstructive hydrocephalus as a result of giant cell tumor of the thoracic spine: A case report
    CHENG-YU WEI, SHUO-TSUNG CHEN, HSU-CHIH TAI, WEN-BING WANG, CHI-CHU CHANG, YAO-CHIN WANG, LI WEI, WOON-MAN KUNG
    Oncology Letters.2016; 11(1): 39.     CrossRef
  • Denosumab for Treatment of a Recurrent Cervical Giant-Cell Tumor
    Daisuke Kajiwara, Hiroto Kamoda, Tsukasa Yonemoto, Shintaro Iwata, Takeshi Ishii, Toshinori Tsukanishi, Seiji Ohtori, Masashi Yamazaki, Akihiko Okawa
    Asian Spine Journal.2016; 10(3): 553.     CrossRef
  • Giant Cell Tumor of the Thoracic Vertebra
    Negar Azarpira, Farshid Javadi, Arash Safarian
    Neurosurgery Quarterly.2015; 25(2): 264.     CrossRef
  • 5,374 View
  • 43 Download
  • 5 Crossref
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