Document Type : Case Report
Department of Neurosurgery, Ibn Sina Diagnostic and Consultation Center, Lalbag, Dhaka, Bangladesh
Consultant, Department of Orthopaedic surgery, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Department of Neurosurgery, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh
Division of Anesthesia,Sardar Womens Hospital, Bapunagar, Ahmedabad, India
Department of Neurological Surgery,Christian Doppler Medical Centre, Laboratory for Microsurgical Neuroanatomy,Paracelsus Medical University,Salzburg, Austria
Neurosurgery Unit,Highly specialised Hospital and National importence,Garibaldi,Catania,Italy
Department of Neurosurgery,Trauma and Gamma Knief Centre,Cannizzaro Hospital,Catania,Italy
Department of Neurosurgery, Bhawani Hospital, Birgunj, Nepal
Background: Spinal hamartoma is an extremely rare lesion for symptomatic spinal cord compression in adult population. Without any association of spinal dysraphism and neurofibromatosis, only 3 cases have been reported in the literature.
Case description: A 40-year-old man presented with lumbago femorica for 6 months. Gradually the symptoms worsened and he developed features of Cauda equina syndrome. Magnetic Resonence Imagimg demonstrated a heterogeneously hyperintense intradural extramedullary mass in both T1 and T2WI, involving conus medullaris and cauda equina, opposite to L1. Patient underwent near total resection of lesion through posterior midline approach. Histopathological features were consistent with hamartoma. Patient neurologically improved and follow up MRI at 6 months showed static small nodular tumor residue.
Conclusion: To the best of our knowledge, current report is the fourth case of spinal hamartoma in adult male, without any association of spinal dysraphism and neurofibromatosis .This may be the first reported case from Bangladesh.