Late spinal cord metastasis of fourth ventricle ependymoma appeared nineteen years after the initial treatment
Autor: | Hirokazu Kawano, Tohru Hayashi, Hidenobu Ochiai, Yoshiya Shimao, Yuzo Yamakawa |
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Rok vydání: | 2009 |
Předmět: |
Ependymoma
Cancer Research medicine.medical_specialty Cerebral Ventricle Neoplasms Spinal Cord Neoplasm Fourth ventricle Metastasis medicine Humans Longitudinal Studies Spinal Cord Neoplasms Fourth Ventricle medicine.diagnostic_test business.industry Magnetic resonance imaging Middle Aged medicine.disease Spinal cord Combined Modality Therapy Magnetic Resonance Imaging Surgery Ki-67 Antigen medicine.anatomical_structure Spinal cord tumor Neurology Oncology Female Neurology (clinical) Radiology Tomography X-Ray Computed business |
Zdroj: | Journal of Neuro-Oncology. 96:295-299 |
ISSN: | 1573-7373 0167-594X |
DOI: | 10.1007/s11060-009-9964-7 |
Popis: | Spinal cord dissemination (metastasis) of a fourth ventricle ependymoma more than ten years after surgical resection is extremely rare. In this report, we present an unusual case of a fourth ventricle ependymoma with metastasis to the thoracic spinal cord 19 years after the initial therapy, but without local recurrence. A 37 year-old patient underwent gross total resection of a fourth ventricle ependymoma and postoperative radiation therapy to the posterior fossa. Computed tomography (CT) scanning and/or magnetic resonance (MR) imaging performed during follow up examinations, conducted annually for ten years after the therapy, revealed no evidence of local tumor recurrence. However, 19 years after the initial treatment, the patient complained of back pain and gait disturbances. MR imaging revealed an intradural extramedullary tumor at the Th2-5 levels. MR imaging of the brain revealed no local tumor recurrence or intracranial tumor dissemination. Cerebrospinal fluid cytology revealed no presence of tumor cells. Total resection of the spinal cord tumor was performed, and the tumor was diagnosed as an ependymoma. We describe the clinical features of this rare lesion and particularly emphasize the need for long-term follow up, for more than ten years after the initial treatment, in patients with fourth ventricle ependymoma. |
Databáze: | OpenAIRE |
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