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Challenging the giant: A case report on a huge sacrococcygeal chordoma and its radiological insights.
Radiol Case Rep
February 2025
Department of Psychiatry, Datta Meghe Institute of Medical Sciences, Sawangi, Wardha, Maharashtra 442001, India.
Sacral chordoma is a rare osseous tumor of malignant origin. Remnants of the notochord in the region of sacrum and coccyx is said to be the origin of these tumors. Patients generally have delayed presentation, which is responsible for larger tumor size.
View Article and Find Full Text PDFPartial Sacrectomy With Lumbopelvic Fixation for Sacral Giant Cell Tumor: Emphasizing Optimal Neuro-Oncological Outcomes.
Cureus
October 2024
Neurosurgery, Dr. D. Y. Patil Medical College, Hospital & Research Centre, Dr. D. Y. Patil Vidyapeeth (Deemed to be University), Pune, IND.
Giant cell tumors (GCTs) of bone are classified as intermediate malignant tumors with a significant potential for local infiltration. Despite their benign histopathological appearance, these tumors exhibit extreme local aggression. The sacrum is the most commonly affected spinal region, followed by the lumbar, cervical, and thoracic regions.
View Article and Find Full Text PDFA Giant Panda's Skin and Hairs Infection of Nannizzia Gypsum on Lumbosacral Region Successfully Treated by Oral Terbinafine and Topic Naftifine-ketoconazole Cream.
Mycopathologia
June 2024
Department of Dermatovenereology, West China Hospital of Sichuan University, Chengdu, China.
Lumbar functional evaluation of pelvic bone sarcomas after surgical resection and spinal pelvic fixation: A clinical study of 304 cases.
Cancer Med
June 2024
Department of Musculoskeletal Tumor, People's Hospital, Peking University, Beijing, China.
Aims: We endeavored to introduce a novel scoring system (Lumbar Functional Index, LFI) capable of evaluating lumbar function in pelvic bone sarcoma patients who underwent surgical resection and spinal pelvic fixation, while simultaneously identifying the incidence, outcomes, and risk factors of lumbar function impairment among these populations.
Patients And Methods: A cohort of 304 primary bone sarcoma patients were recruited. The LFI was created based on the Oswestry Dysfunction Index (ODI) and Japanese Orthopaedic Association (JOA) scores.
Concurrent spinal meningioma and giant invasive schwannoma without neurofibromatosis in children: A case report and literature review.
Childs Nerv Syst
May 2024
Department of Neurosurgery, The First Hospital of Hebei Medical University, 89# Dong-Gang Road, Hebei Province, Shijiazhuang, 050000, China.
Article Synopsis
- Spinal meningiomas and schwannomas occurring together in patients without neurofibromatosis are very rare, with only 15 cases recorded so far.
- A case study highlights a 15-year-old child with both a dorsal meningioma and a large invasive ventral schwannoma located at different spinal levels, which led to significant bone erosion.
- The successful surgical removal of the tumors, using a non-fusion approach, aims to maintain lumbar spine function, but the underlying causes and clinical symptoms of these tumors remain unclear.
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