Your browser doesn't support javascript.
loading
Spinal Malignant Peripheral Nerve Sheath Tumours in Nigerians.
Oyemolade, T A; Adeolu, A A; Malomo, A O; Salami, A A; Idowu, O K.
Afiliación
  • Oyemolade TA; Department of Neurological Surgery,University College Hospital, Ibadan, Nigeria.
  • Adeolu AA; Department of Neurological Surgery,University College Hospital, Ibadan, Nigeria and College of Medicine, University of Ibadan,Nigeria.
  • Malomo AO; Department of Neurological Surgery,University College Hospital, Ibadan, Nigeria and College of Medicine, University of Ibadan,Nigeria.
  • Salami AA; Department of Pathology,College of Medicine, University of Ibadan,Nigeria.
  • Idowu OK; Department of Anaesthesia,College of Medicine, University of Ibadan,Nigeria.
West Afr J Med ; 38(1): 93-97, 2021 01.
Article en En | MEDLINE | ID: mdl-33463714
BACKGROUND: Spinal Malignant peripheral nerve sheath tumours (MPNSTs) are very rare aggressive tumours with poor prognosis. Little is known about these tumours in sub-saharan Africa. OBJECTIVES: This study aims to evaluate the clinical profile and outcome of management of these tumours in a resource limited country. METHODS: We retrospectively analysed data from the records of patients who had surgery for spinal MPNSTs at our center between January 2004 and December 2018. RESULTS: There were four patients in this study (M:F= 1:1). The ages ranged from 27-53 years with a mean of 43.25 ± 11.84 years. The tumour was located in the thoracic region in 2 of the patients (50%), the lumbar region in one (25%) and thoracolumbar in the 4th patient. Three patients (75%) presented with back pain while limb weakness, sensory deficit and sphincteric dysfunction were present in all patients at presentation. The duration of symptoms were 2 months in 2 patients (50%) and 3 months in the other 2. None of the patients had neurofibromatosis. Gross total tumour excision was achieved in 2 patients (50%) and subtotal resection in the other 2. The tumours were high grade in three patients (75%) and low grade in one. Two patients had adjuvant radiotherapy. Two of the patients were dead within 6 months of the diagnosis, another one within 18 months while one patient is still alive 3 years after. CONCLUSIONS: MPNSTs are very rare in our practice. Most of the tumours were high grade tumours and ran an aggressive course.
Asunto(s)
Buscar en Google
Base de datos: MEDLINE Asunto principal: Neurofibrosarcoma / Neoplasias de la Vaina del Nervio Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Africa Idioma: En Revista: West Afr J Med Año: 2021 Tipo del documento: Article
Buscar en Google
Base de datos: MEDLINE Asunto principal: Neurofibrosarcoma / Neoplasias de la Vaina del Nervio Tipo de estudio: Diagnostic_studies / Observational_studies / Prognostic_studies / Risk_factors_studies País/Región como asunto: Africa Idioma: En Revista: West Afr J Med Año: 2021 Tipo del documento: Article