1) Malignant cervical spine tumors can be primary tumors of the spine or metastatic tumors that spread from other locations like the lung, breast, or prostate.
2) Primary malignant tumors of the cervical spine are rare but include osteosarcoma, chordoma, and lymphoma. Metastatic tumors to the cervical spine are more common.
3) Clinical symptoms of metastatic spinal tumors include pain, neurologic deficits, and pathologic spinal fractures caused by tumor infiltration or compression of the spinal cord or nerves.
The document discusses the historical perspectives and principles of limb salvage surgery for malignant bone sarcomas. It notes that before the 1970s, amputation was standard treatment but survival rates were low. Developments in chemotherapy in the 1970s-80s improved outcomes. Neoadjuvant chemotherapy provided pre-op tumor downstaging while the patient awaited surgery. Modern imaging allows better staging and understanding of tumor extent. With multimodal treatment including chemotherapy and improved surgical techniques, 80-85% of patients can now be treated with limb-preserving wide resection. Limb salvage provides similar survival benefits to amputation.
This document describes several cases of classic osteosarcoma. It begins with an overview of classic osteosarcoma, including that it most commonly affects children and young adults, occurs in long bones like the femur and tibia, and patients typically present with pain followed by a tumor mass. It then describes the staging process and treatments, including chemotherapy and surgical resection. Multiple patient cases are then described in detail, with imaging findings, surgical procedures, outcomes, and in some cases, recurrence of disease.
This document provides information on Ewing sarcoma, a rare type of cancer that develops in bone or soft tissue. It discusses the epidemiology, pathology, clinical features, workup including imaging and staging, prognostic factors, management with chemotherapy, surgery and/or radiation therapy, and clinical trials. Ewing sarcoma is most common in children and young adults between ages 10-20. It is characterized by small, blue round cells and specific gene translocations. Treatment involves induction chemotherapy followed by local control with surgery or radiation and maintenance chemotherapy for at least 28-49 weeks. Prognostic factors and long term follow up care are also outlined.
The document describes several variants of osteosarcoma, including hemorrhagic, parosteal, and periosteal osteosarcoma. Hemorrhagic osteosarcoma is a very lytic and hemorrhagic variant that can resemble an aneurysmal bone cyst. Parosteal osteosarcoma arises on the surface of bone and has a good prognosis. Periosteal osteosarcoma contains cartilage and arises from long bones, typically in the second decade of life. Each variant is illustrated through case examples showing imaging, specimens, and histology.
This document provides a summary of 50 cases of osteoid osteoma and osteoblastoma. Case 1-50 cover osteoid osteoma, with the classic presentation of a painful nidus most commonly in long bones that is diagnosed using imaging such as CT scan and bone scan. Case 51-94 cover osteoblastoma, a larger variant of osteoid osteoma that is treated surgically via curettage. The remainder of cases provide further examples and variations of these two conditions.
Metastatic Tumors of the Spinal Column: Diagnosis and TreatmentGeorge Sapkas
1. The document discusses metastatic tumors of the spinal column, including their diagnosis and treatment. It provides information on the epidemiology, clinical symptoms, diagnosis, and various treatment options.
2. Treatment options discussed include medical treatments like chemotherapy, radiotherapy, and biophosphonates. Surgical treatments include decompression, spondylodesis, debulking, and total en bloc vertebrectomy. Factors in determining the appropriate treatment include the type and location of cancer, pain level, neurological status, and life expectancy.
3. Outcomes of surgical treatments like spondylectomy and decompression with stabilization in 45 patients over 12 years were analyzed. Most patients experienced pain relief and neurological improvement
This document describes several fibrous soft tissue tumors including desmoid tumors, aponeuratic fibroma, infantile fibromatosis, elastofibroma, and nodular fascitis. It provides details on the typical presentation, location, patient demographics, histological features, treatment and prognosis for each tumor type. Several case examples are also described with accompanying imaging findings and histopathology.
The document discusses the historical perspectives and principles of limb salvage surgery for malignant bone sarcomas. It notes that before the 1970s, amputation was standard treatment but survival rates were low. Developments in chemotherapy in the 1970s-80s improved outcomes. Neoadjuvant chemotherapy provided pre-op tumor downstaging while the patient awaited surgery. Modern imaging allows better staging and understanding of tumor extent. With multimodal treatment including chemotherapy and improved surgical techniques, 80-85% of patients can now be treated with limb-preserving wide resection. Limb salvage provides similar survival benefits to amputation.
This document describes several cases of classic osteosarcoma. It begins with an overview of classic osteosarcoma, including that it most commonly affects children and young adults, occurs in long bones like the femur and tibia, and patients typically present with pain followed by a tumor mass. It then describes the staging process and treatments, including chemotherapy and surgical resection. Multiple patient cases are then described in detail, with imaging findings, surgical procedures, outcomes, and in some cases, recurrence of disease.
This document provides information on Ewing sarcoma, a rare type of cancer that develops in bone or soft tissue. It discusses the epidemiology, pathology, clinical features, workup including imaging and staging, prognostic factors, management with chemotherapy, surgery and/or radiation therapy, and clinical trials. Ewing sarcoma is most common in children and young adults between ages 10-20. It is characterized by small, blue round cells and specific gene translocations. Treatment involves induction chemotherapy followed by local control with surgery or radiation and maintenance chemotherapy for at least 28-49 weeks. Prognostic factors and long term follow up care are also outlined.
The document describes several variants of osteosarcoma, including hemorrhagic, parosteal, and periosteal osteosarcoma. Hemorrhagic osteosarcoma is a very lytic and hemorrhagic variant that can resemble an aneurysmal bone cyst. Parosteal osteosarcoma arises on the surface of bone and has a good prognosis. Periosteal osteosarcoma contains cartilage and arises from long bones, typically in the second decade of life. Each variant is illustrated through case examples showing imaging, specimens, and histology.
This document provides a summary of 50 cases of osteoid osteoma and osteoblastoma. Case 1-50 cover osteoid osteoma, with the classic presentation of a painful nidus most commonly in long bones that is diagnosed using imaging such as CT scan and bone scan. Case 51-94 cover osteoblastoma, a larger variant of osteoid osteoma that is treated surgically via curettage. The remainder of cases provide further examples and variations of these two conditions.
Metastatic Tumors of the Spinal Column: Diagnosis and TreatmentGeorge Sapkas
1. The document discusses metastatic tumors of the spinal column, including their diagnosis and treatment. It provides information on the epidemiology, clinical symptoms, diagnosis, and various treatment options.
2. Treatment options discussed include medical treatments like chemotherapy, radiotherapy, and biophosphonates. Surgical treatments include decompression, spondylodesis, debulking, and total en bloc vertebrectomy. Factors in determining the appropriate treatment include the type and location of cancer, pain level, neurological status, and life expectancy.
3. Outcomes of surgical treatments like spondylectomy and decompression with stabilization in 45 patients over 12 years were analyzed. Most patients experienced pain relief and neurological improvement
This document describes several fibrous soft tissue tumors including desmoid tumors, aponeuratic fibroma, infantile fibromatosis, elastofibroma, and nodular fascitis. It provides details on the typical presentation, location, patient demographics, histological features, treatment and prognosis for each tumor type. Several case examples are also described with accompanying imaging findings and histopathology.
A comprehensive presentation on the epidemiology, pathophysiology, clinical presentation, decision making and treatment options of spinal metastases. Supported with the best available evidence as of October 6, 2008
This document discusses numerous cases of patients presenting with bone lesions that were initially suspected to be metastatic disease but were later determined to be other diagnoses. Case 1169 describes a 47-year-old female whose stress fracture of the femoral neck was mistaken for a metastatic lesion. Imaging and biopsy revealed the lesion was actually a pseudotumor caused by osteoporosis. Similarly, Case 1169.1 involves a 43-year-old female on steroids whose bilateral hip pain was from stress fractures, not metastases as indicated on her bone scan. The document emphasizes that various benign bone conditions can resemble metastatic bone cancer on imaging and biopsy is often needed for accurate diagnosis.
This document discusses giant cell tumor of bone (GCT), a benign bone tumor typically seen in young adults. It most commonly occurs in the ends of long bones near joints like the knee. The tumor is lytic and geographic on x-ray. Treatment typically involves aggressive curettage followed by packing the defect with bone graft or cement, with a 5-10% recurrence rate. Even though considered benign, 1-2% of GCTs can metastasize to the lungs. Radiation can increase risk of malignant transformation. Several case examples are presented demonstrating features, treatment approaches, and outcomes of GCT in various bone locations.
An Atlas of Musculoskeletal Oncology: Volume 2Amber Caldwell
This document discusses several cases of classic osteosarcoma. It begins with case 108, describing a 16-year-old male with classic osteosarcoma in the femur. It then moves to case 451, describing a 17-year-old male. Several other cases are then summarized, describing patients of varying ages with classic osteosarcoma located in different bones including the femur, tibia, fibula, and humerus. For each case, relevant imaging, specimens, and treatments are briefly discussed.
The document discusses eosinophilic granuloma, a benign histiocytic disorder most commonly seen in children ages 5-15. It often presents as inflammatory bone pain and can resemble conditions like Ewing's sarcoma on x-ray with its permeative, onion-skin appearance. Microscopically, biopsies show large pale histiocytes speckled with eosinophils. Treatment involves surgical curettage or resection for symptomatic relief with a good prognosis.
This document provides an overview of intramedullary spinal cord tumors including their anatomy, classification, clinical presentation, diagnostic workup, treatment and prognosis. Key tumor types discussed include ependymomas, astrocytomas and intramedullary spinal cord metastases. Surgical resection is the primary treatment when possible, along with radiation and chemotherapy in some cases. Prognosis depends on tumor histology, grade, extent of resection and patient's pre-operative neurological status.
This document discusses metastatic carcinoma to bone. It notes that the spine is the most common site of metastatic disease. Breast cancer is the most common cause of bone metastases in women, while prostate cancer is most common in men. Metastases typically appear lytic on x-ray but may have a sclerotic component. Treatment involves radiation, chemotherapy, surgery such as fixation of fractures, or vertebroplasty for spinal metastases. Case studies demonstrate various presentations of bone metastases from primary cancers such as breast, prostate, lung, kidney and thyroid.
A 35yrs young patient, presented to the hospital with lower extremities neurological deficit, radiological investigation showed bony lesion in the posterior elements of T10 causing severe compression on the cord, emergency surgery was performed to decompress the spinal cord, the microscopic examination revealed that lesion was “ aneurysmal bone cyst”.
This document discusses malignant spinal cord compression, its causes, symptoms, diagnosis and treatment. It begins by differentiating between extramedullary vs intradural vs intramedullary compression. Common symptoms include pain, motor deficits, sensory changes and autonomic dysfunction. Metastatic tumors are the most frequent cause. Diagnosis involves imaging like MRI, CT and bone scans. Treatment aims to relieve pain and prevent further cord compression, and may involve surgery, radiation or supportive care depending on the extent of disease and patient prognosis. Early detection and treatment can help preserve neurological function.
Ewing's sarcoma is a rare cancer that affects bones or soft tissue. It is characterized by small, round cancer cells and commonly affects children and young adults. Treatment involves induction chemotherapy, followed by local therapy with surgery or radiation if possible, along with additional maintenance chemotherapy. The multimodal approach has improved survival rates in recent decades, though long-term outcomes remain challenging due to the risk of recurrence or secondary cancers.
This document discusses various types of spinal tumors, including their location, characteristics, and MRI appearances. It covers primary spinal tumors such as schwannomas, neurofibromas, meningiomas, ependymomas, astrocytomas, and hemangioblastomas. It describes these tumors' demographics, symptoms, classification as interdural exteramedullary or interdural intramedullary, and features on T1-, T2-, and contrast-enhanced MRI sequences. Rare tumors like lipomas, paragangliomas, and subependymomas are also outlined briefly.
Vertebral Column Tumors
Primary tumors: These tumors occur in the vertebral column, and grow either from the bone or disc elements of the spine. They typically occur in younger adults. Osteogenic sarcoma (osteosarcoma) is the most common malignant bone tumor. Most primary spinal tumors are quite rare and usually grow slowly.
Metastatic tumors: Most often, spinal tumors metastasize (spread) from cancer in another area of the body , These tumors usually produce pain that does not get better with rest, may be worse at night, and is often accompanied by other signs of serious illness (such as weight loss, fever/chills/shakes, nausea or vomiting).
Identified in 1921 by James Ewing
2nd most common bone tumor in children
Ewing’s Sarcoma Family of tumors:
Ewing’s sarcoma (Bone –87%)
Extraosseous Ewing’s sarcoma (8%)
Peripheral PNET(5%)
Askin’s tumor
This document describes various neurogenic soft tissue tumors including neurilemoma, solitary neurofibroma, and neurofibromatosis. Neurilemoma is a benign schwannoma arising from peripheral nerve sheath. Solitary neurofibroma is a fusiform nerve sheath tumor located centrally within a peripheral nerve. Neurofibromatosis is a genetic condition characterized by numerous cutaneous neurofibromas and large plexiform neurofibromas involving peripheral nerves. Representative cases of each tumor are described with associated imaging findings and histology.
Tumors of the vertebral column are rare, comprising less than 10% of all primary bony tumors. The most common benign tumor is osteoid osteoma, while multiple myeloma is the most common malignant tumor. Imaging modalities such as CT and MRI scans are used to evaluate the lesions and determine the extent of involvement. An accurate diagnosis is essential to determine the appropriate treatment, which may include surgery, radiation therapy, or chemotherapy.
Spinal cord lesions and its radiological imaging finding.Navneet Ranjan
1. The document discusses imaging approaches for evaluating intramedullary spinal cord lesions. It outlines a systematic approach including assessing the lesion length, extent of cord involvement, location within the cord, cord swelling, and enhancement characteristics.
2. Differential diagnoses discussed include demyelinating diseases, tumors, vascular causes, and infections. Specific conditions like multiple sclerosis, neuromyelitis optica, transverse myelitis, and various tumor types are described.
3. Imaging features of different pathologies are provided to help differentiate between conditions like ependymoma, astrocytoma, ganglioglioma, and hemangioblastoma.
1) A 50-year-old male presented with left leg pain and swelling for 3 months prior to a falling accident. Imaging showed a pathologic fracture of the left tibia.
2) Biopsy revealed high-grade conventional osteosarcoma. The patient received neoadjuvant chemotherapy with cisplatin and adriamycin.
3) After mid-cycle evaluation, the patient underwent surgery for resection of the tumor followed by adjuvant chemotherapy.
This document describes various types of benign soft tissue tumors, including several variants of lipomas. Superficial lipomas are the most common soft tissue tumor seen in orthopedic oncology, typically occurring in older patients on the back, shoulders, and neck. Intramuscular lipomas occur deeper in larger muscle groups between ages 30-60. Spindle cell lipomas are seen more in men ages 45-65 in the neck or shoulder. Angiolipomas occur in younger adults and are often painful due to increased vascularity. Ossifying lipomas are rare, with bone and cartilage present within the lipoma tissue. Imaging and histologic features of each variant are provided.
Bone sarcomas are rare cancers that can be curable if treated properly. The main types are osteosarcoma, Ewing sarcoma, and chondrosarcoma. Staging involves imaging and biopsy to determine tumor size, location, and spread. Multidisciplinary teams are needed for optimal care. Chemotherapy is important for osteosarcoma and Ewing sarcoma but not usually effective for chondrosarcoma. Neoadjuvant chemotherapy followed by surgery improves outcomes for osteosarcoma over surgery alone. Short and long chemotherapy regimens appear equally effective for operable osteosarcoma. Ifosfamide added to standard regimens improves outcomes for non-metastatic and
Intradural extramedullary mass - a case on MRIREKHAKHARE
An 18-year-old boy presented with 6 months of lower back pain and lower extremity weakness on the left side. MRI revealed two masses - an intradural extramedullary mass between D10-D12 deviating the spinal cord to the right, and a long paravertebral mass extending from T7-L1. The intradural mass enhanced with contrast and was considered to be an intradural extramedullary lesion such as a neurofibroma. The patient was referred for surgical management and biopsy to determine the exact diagnosis.
This document discusses spinal tumors, including:
1. Spinal tumors can be primary or secondary, extradural or intradural. The most common symptoms are pain and neurological deficits.
2. Common primary tumors include hemangiomas, aneurysmal bone cysts, and chordomas. Metastatic tumors are most frequently from breast, prostate and lung cancers.
3. Imaging like CT, MRI and bone scans are used to identify the location and extent of tumors. Tissue biopsy is needed to confirm diagnosis.
4. Treatment involves a multidisciplinary approach with surgery, radiation, chemotherapy and steroid/medical management. The goal of surgery is wide or en bloc resection with spinal reconstruction and stabilization
The skeleton is a common site for metastatic spread of cancer. Secondary bone cancer most often presents with bone pain. Diagnosis involves imaging tests like x-rays, CT scans, MRIs, and bone scans. Treatment includes pain medications, chemotherapy/hormonal therapy for the primary cancer, radiation therapy, and bisphosphonates. Surgery may be needed for complications like fractures.
A comprehensive presentation on the epidemiology, pathophysiology, clinical presentation, decision making and treatment options of spinal metastases. Supported with the best available evidence as of October 6, 2008
This document discusses numerous cases of patients presenting with bone lesions that were initially suspected to be metastatic disease but were later determined to be other diagnoses. Case 1169 describes a 47-year-old female whose stress fracture of the femoral neck was mistaken for a metastatic lesion. Imaging and biopsy revealed the lesion was actually a pseudotumor caused by osteoporosis. Similarly, Case 1169.1 involves a 43-year-old female on steroids whose bilateral hip pain was from stress fractures, not metastases as indicated on her bone scan. The document emphasizes that various benign bone conditions can resemble metastatic bone cancer on imaging and biopsy is often needed for accurate diagnosis.
This document discusses giant cell tumor of bone (GCT), a benign bone tumor typically seen in young adults. It most commonly occurs in the ends of long bones near joints like the knee. The tumor is lytic and geographic on x-ray. Treatment typically involves aggressive curettage followed by packing the defect with bone graft or cement, with a 5-10% recurrence rate. Even though considered benign, 1-2% of GCTs can metastasize to the lungs. Radiation can increase risk of malignant transformation. Several case examples are presented demonstrating features, treatment approaches, and outcomes of GCT in various bone locations.
An Atlas of Musculoskeletal Oncology: Volume 2Amber Caldwell
This document discusses several cases of classic osteosarcoma. It begins with case 108, describing a 16-year-old male with classic osteosarcoma in the femur. It then moves to case 451, describing a 17-year-old male. Several other cases are then summarized, describing patients of varying ages with classic osteosarcoma located in different bones including the femur, tibia, fibula, and humerus. For each case, relevant imaging, specimens, and treatments are briefly discussed.
The document discusses eosinophilic granuloma, a benign histiocytic disorder most commonly seen in children ages 5-15. It often presents as inflammatory bone pain and can resemble conditions like Ewing's sarcoma on x-ray with its permeative, onion-skin appearance. Microscopically, biopsies show large pale histiocytes speckled with eosinophils. Treatment involves surgical curettage or resection for symptomatic relief with a good prognosis.
This document provides an overview of intramedullary spinal cord tumors including their anatomy, classification, clinical presentation, diagnostic workup, treatment and prognosis. Key tumor types discussed include ependymomas, astrocytomas and intramedullary spinal cord metastases. Surgical resection is the primary treatment when possible, along with radiation and chemotherapy in some cases. Prognosis depends on tumor histology, grade, extent of resection and patient's pre-operative neurological status.
This document discusses metastatic carcinoma to bone. It notes that the spine is the most common site of metastatic disease. Breast cancer is the most common cause of bone metastases in women, while prostate cancer is most common in men. Metastases typically appear lytic on x-ray but may have a sclerotic component. Treatment involves radiation, chemotherapy, surgery such as fixation of fractures, or vertebroplasty for spinal metastases. Case studies demonstrate various presentations of bone metastases from primary cancers such as breast, prostate, lung, kidney and thyroid.
A 35yrs young patient, presented to the hospital with lower extremities neurological deficit, radiological investigation showed bony lesion in the posterior elements of T10 causing severe compression on the cord, emergency surgery was performed to decompress the spinal cord, the microscopic examination revealed that lesion was “ aneurysmal bone cyst”.
This document discusses malignant spinal cord compression, its causes, symptoms, diagnosis and treatment. It begins by differentiating between extramedullary vs intradural vs intramedullary compression. Common symptoms include pain, motor deficits, sensory changes and autonomic dysfunction. Metastatic tumors are the most frequent cause. Diagnosis involves imaging like MRI, CT and bone scans. Treatment aims to relieve pain and prevent further cord compression, and may involve surgery, radiation or supportive care depending on the extent of disease and patient prognosis. Early detection and treatment can help preserve neurological function.
Ewing's sarcoma is a rare cancer that affects bones or soft tissue. It is characterized by small, round cancer cells and commonly affects children and young adults. Treatment involves induction chemotherapy, followed by local therapy with surgery or radiation if possible, along with additional maintenance chemotherapy. The multimodal approach has improved survival rates in recent decades, though long-term outcomes remain challenging due to the risk of recurrence or secondary cancers.
This document discusses various types of spinal tumors, including their location, characteristics, and MRI appearances. It covers primary spinal tumors such as schwannomas, neurofibromas, meningiomas, ependymomas, astrocytomas, and hemangioblastomas. It describes these tumors' demographics, symptoms, classification as interdural exteramedullary or interdural intramedullary, and features on T1-, T2-, and contrast-enhanced MRI sequences. Rare tumors like lipomas, paragangliomas, and subependymomas are also outlined briefly.
Vertebral Column Tumors
Primary tumors: These tumors occur in the vertebral column, and grow either from the bone or disc elements of the spine. They typically occur in younger adults. Osteogenic sarcoma (osteosarcoma) is the most common malignant bone tumor. Most primary spinal tumors are quite rare and usually grow slowly.
Metastatic tumors: Most often, spinal tumors metastasize (spread) from cancer in another area of the body , These tumors usually produce pain that does not get better with rest, may be worse at night, and is often accompanied by other signs of serious illness (such as weight loss, fever/chills/shakes, nausea or vomiting).
Identified in 1921 by James Ewing
2nd most common bone tumor in children
Ewing’s Sarcoma Family of tumors:
Ewing’s sarcoma (Bone –87%)
Extraosseous Ewing’s sarcoma (8%)
Peripheral PNET(5%)
Askin’s tumor
This document describes various neurogenic soft tissue tumors including neurilemoma, solitary neurofibroma, and neurofibromatosis. Neurilemoma is a benign schwannoma arising from peripheral nerve sheath. Solitary neurofibroma is a fusiform nerve sheath tumor located centrally within a peripheral nerve. Neurofibromatosis is a genetic condition characterized by numerous cutaneous neurofibromas and large plexiform neurofibromas involving peripheral nerves. Representative cases of each tumor are described with associated imaging findings and histology.
Tumors of the vertebral column are rare, comprising less than 10% of all primary bony tumors. The most common benign tumor is osteoid osteoma, while multiple myeloma is the most common malignant tumor. Imaging modalities such as CT and MRI scans are used to evaluate the lesions and determine the extent of involvement. An accurate diagnosis is essential to determine the appropriate treatment, which may include surgery, radiation therapy, or chemotherapy.
Spinal cord lesions and its radiological imaging finding.Navneet Ranjan
1. The document discusses imaging approaches for evaluating intramedullary spinal cord lesions. It outlines a systematic approach including assessing the lesion length, extent of cord involvement, location within the cord, cord swelling, and enhancement characteristics.
2. Differential diagnoses discussed include demyelinating diseases, tumors, vascular causes, and infections. Specific conditions like multiple sclerosis, neuromyelitis optica, transverse myelitis, and various tumor types are described.
3. Imaging features of different pathologies are provided to help differentiate between conditions like ependymoma, astrocytoma, ganglioglioma, and hemangioblastoma.
1) A 50-year-old male presented with left leg pain and swelling for 3 months prior to a falling accident. Imaging showed a pathologic fracture of the left tibia.
2) Biopsy revealed high-grade conventional osteosarcoma. The patient received neoadjuvant chemotherapy with cisplatin and adriamycin.
3) After mid-cycle evaluation, the patient underwent surgery for resection of the tumor followed by adjuvant chemotherapy.
This document describes various types of benign soft tissue tumors, including several variants of lipomas. Superficial lipomas are the most common soft tissue tumor seen in orthopedic oncology, typically occurring in older patients on the back, shoulders, and neck. Intramuscular lipomas occur deeper in larger muscle groups between ages 30-60. Spindle cell lipomas are seen more in men ages 45-65 in the neck or shoulder. Angiolipomas occur in younger adults and are often painful due to increased vascularity. Ossifying lipomas are rare, with bone and cartilage present within the lipoma tissue. Imaging and histologic features of each variant are provided.
Bone sarcomas are rare cancers that can be curable if treated properly. The main types are osteosarcoma, Ewing sarcoma, and chondrosarcoma. Staging involves imaging and biopsy to determine tumor size, location, and spread. Multidisciplinary teams are needed for optimal care. Chemotherapy is important for osteosarcoma and Ewing sarcoma but not usually effective for chondrosarcoma. Neoadjuvant chemotherapy followed by surgery improves outcomes for osteosarcoma over surgery alone. Short and long chemotherapy regimens appear equally effective for operable osteosarcoma. Ifosfamide added to standard regimens improves outcomes for non-metastatic and
Intradural extramedullary mass - a case on MRIREKHAKHARE
An 18-year-old boy presented with 6 months of lower back pain and lower extremity weakness on the left side. MRI revealed two masses - an intradural extramedullary mass between D10-D12 deviating the spinal cord to the right, and a long paravertebral mass extending from T7-L1. The intradural mass enhanced with contrast and was considered to be an intradural extramedullary lesion such as a neurofibroma. The patient was referred for surgical management and biopsy to determine the exact diagnosis.
This document discusses spinal tumors, including:
1. Spinal tumors can be primary or secondary, extradural or intradural. The most common symptoms are pain and neurological deficits.
2. Common primary tumors include hemangiomas, aneurysmal bone cysts, and chordomas. Metastatic tumors are most frequently from breast, prostate and lung cancers.
3. Imaging like CT, MRI and bone scans are used to identify the location and extent of tumors. Tissue biopsy is needed to confirm diagnosis.
4. Treatment involves a multidisciplinary approach with surgery, radiation, chemotherapy and steroid/medical management. The goal of surgery is wide or en bloc resection with spinal reconstruction and stabilization
The skeleton is a common site for metastatic spread of cancer. Secondary bone cancer most often presents with bone pain. Diagnosis involves imaging tests like x-rays, CT scans, MRIs, and bone scans. Treatment includes pain medications, chemotherapy/hormonal therapy for the primary cancer, radiation therapy, and bisphosphonates. Surgery may be needed for complications like fractures.
Dr. Ledian Fezollari's document discusses bone tumors. It begins by stating that primary malignant bone tumors make up 1% of all cancers and the most common bone tumor is metastases from other sites. The WHO classification of bone tumors is mentioned. Clinical presentation depends on age, with most benign tumors in children and myeloma most common over age 70. Investigations include imaging like radiography, CT, MRI, and biopsy. Treatment depends on tumor type and stage, and may involve chemotherapy, surgery such as limb salvage or amputation, and radiotherapy.
Dr. Ledian Fezollari discusses bone tumors in a document covering their classification, clinical presentation, investigations and treatment. Some key points:
- Primary malignant bone tumors make up 1% of all cancers but secondary bone tumors from other sites are more common.
- Presentation depends on age, with childhood cancers like osteosarcoma and Ewing's sarcoma more common. Myeloma is the most common bone tumor in those over 70.
- Investigations include imaging like x-rays, CT and MRI to determine location and extent of the tumor. Biopsies are also important.
- Treatment depends on tumor type and stage but may include chemotherapy, surgery like limb salvage procedures
Primary tumors of the spine require special treatment considerations due to the biomechanical and neurological structures of the spine. Common benign primary spine tumors include osteoid osteoma, osteoblastoma, aneurysmal bone cyst, and Langerhans cell histiocytosis. Osteoid osteoma typically presents as a painful lytic lesion best seen on CT. Osteoblastoma and aneurysmal bone cyst are expansile lesions that can be locally aggressive. Treatment involves complete surgical excision or embolization with the goal of preventing recurrence. Langerhans cell histiocytosis commonly affects children and adolescents, presenting as vertebral flattening with self-limited symptoms in many cases.
Metastatic bone tumors are most commonly caused by cancer spreading from another primary site to the bones. Approximately 50% of cancers can metastasize to the skeleton, with the most common sites being the vertebrae, pelvis, femur, ribs, humerus and skull. The presentation may include bone pain, pathologic fractures, masses, or neurological impairment. Diagnosis involves history, physical exam, imaging like x-rays, CT, MRI and bone scans. Treatment depends on cancer type but often includes radiation, chemotherapy, hormone therapy, surgery and bisphosphonates. Local therapies aim to destroy cancer cells at the specific bone site while systemic therapies target cells throughout the body.
Ewing sarcoma is the second most common malignant bone tumor in children. It occurs most commonly in patients between 5-25 years old. Diagnosis involves imaging like MRI and CT to identify bone destruction and soft tissue involvement. Pathology shows small, blue, round cells. Treatment involves induction chemotherapy followed by surgery or radiation if possible to achieve wide resection margins, with additional maintenance chemotherapy to reduce risk of metastasis, most commonly to lungs and bones. Prognosis depends on ability to achieve wide surgical resection and response to chemotherapy. Five-year survival has improved to over 70% with current multimodal treatment approaches.
The document discusses several types of primary bone cancers. It focuses on chondrosarcoma, which arises from cartilage and most commonly affects the pelvis and femur in older adults. The document outlines diagnostic evaluation, staging, histologic grading, and treatment approaches including wide local excision and adjuvant therapies for chondrosarcoma. Prognosis depends on tumor grade and location. Ewing's sarcoma and osteosarcoma are also discussed as well as giant cell tumor of bone.
This document discusses the management of rhabdomyosarcoma, a type of soft tissue sarcoma that is most common in children. It begins by covering the epidemiology, risk factors, clinical presentation and symptoms. Diagnostic workup involves tumor biopsy along with imaging like CT, MRI and PET scans to determine tumor location and spread. Staging uses the Children's Oncology Group system which considers tumor site, size, margins after surgery, and metastasis. There are various histologic subtypes with differing prognoses - embryonal has intermediate prognosis while alveolar and undifferentiated subtypes have poorer outcomes. Treatment involves chemotherapy, surgery and radiation therapy tailored to stage and risk group.
This document provides an overview of rhabdomyosarcoma (RMS), a rare soft tissue cancer that occurs mostly in children. It discusses the epidemiology, risk factors, clinical presentation, diagnostic workup, staging, histologic subtypes and prognosis of RMS. RMS most commonly occurs in the head, neck, genitourinary tract and extremities. Diagnostic testing includes biopsy, imaging like CT/MRI and bone marrow aspiration. Staging involves tumor size, location, margins and metastasis. The prognosis depends on the histologic subtype, with botryoid and spindle cell having the best outcomes and alveolar/undifferentiated having poorer outcomes.
Metastatic Tumors of the Spinal Column George Sapkas
This document discusses metastatic tumors of the spinal column, including their diagnosis and management. Some key points:
- The thoracolumbar region is the most common location for skeletal metastases, affecting around 70% of patients. The lumbar and sacral spine make up around 20% while the cervical spine is around 10%.
- Treatment options include medical therapies like chemotherapy, hormone therapy, biophosphonates and radiotherapy. Surgical options include decompression, debulking, or excision with or without stabilization. Factors like life expectancy, tumor type and location help determine the best treatment approach.
- Systems like Tokuhashi and Tomita aim to evaluate prognosis and help decide between palliative
Spinal tumors can be classified as extradural, intradural/extramedullary, or intramedullary based on their location. Extradural tumors are most common and often metastatic, while intradural tumors are rare and usually involve nerve sheath tumors or meningiomas. Primary spinal tumors can be benign or malignant, with benign tumors not invading other tissues and malignant tumors potentially spreading. Symptoms depend on tumor location and can include weakness, pain, numbness, and loss of bowel/bladder control. Treatment involves surgery to remove the tumor when possible along with radiation and chemotherapy for malignant tumors. Many benign and malignant tumor types are described in the document.
Primary bone tumors of the spine are rare, accounting for only 4.2% of spinal tumors. This study summarizes the experience of treating 18 cases of primary bone tumors of the spine over 10 years at two hospitals in Bangladesh. The most common tumors were malignant (61%), with the dorsal and lumbar spine being most commonly involved. Pain was the primary presenting symptom in most cases. Surgical treatment with the aim of complete resection when possible combined with preservation of neurological function and spinal stabilization was performed. Adjuvant chemotherapy and radiation were also used. Outcomes were improved pain and function, though malignant tumors often had poorer outcomes and higher mortality. Early diagnosis and multidisciplinary treatment were concluded to be important for managing these rare tumors
Primary bone tumors are rare, accounting for only 0.2-0.5% of all tumors. The majority of bone tumors are secondary metastases rather than primary tumors. Primary bone tumors are classified based on the cell of origin and can be benign or malignant. Benign bone tumors are more common in children and adolescents while malignant tumors typically present in older age groups. Diagnosis involves clinical presentation, imaging studies such as x-ray and biopsy. Treatment depends on whether the tumor is benign or malignant and the specific type and stage of tumor.
This document discusses oropharyngeal cancers. It begins with the anatomy of the oropharynx and its boundaries. It then discusses the epidemiology, risk factors, clinical features, staging, workup, and management of oropharyngeal cancers. Early stage cancers are often treated with either radiotherapy or surgery alone, while locoregionally advanced cancers may be treated with surgery followed by radiation and chemotherapy or with primary chemoradiation. HPV-associated oropharyngeal cancers often have a better prognosis than HPV-negative cancers.
Dr. Yashveer Singh presented on primary vertebral body tumors. He discussed the different types of benign primary tumors that can occur including osteochondroma, hemangioma, eosinophilic granuloma, aneurysmal bone cyst, osteoid osteoma, and osteoblastoma. The presentation covered the pathology, clinical features, radiologic evaluation, and management of each tumor type. Pain is usually the primary symptom, and treatment involves surgery, embolization, or other procedures depending on the specific tumor and symptoms.
Highly malignant tumor of mesenchymal origin.Spindle shaped cells that produce osteoid.2nd most common primary malignant bone tumor after MM.Incidence – 1 to 3 per million per year
Treated by chemo,amputation or rotationplasty
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Cervical spine tumors ioannina 5 5-2014
1. Malignant Cervical
Spine Tumors
Operative treatment
G. SAPKAS
Professor in Orthopedics
Orthopaedic Department
for
Spinal and Musculoskeletal Disorders
“Metropolitan” Hospital
3. Primary tumorsPrimary tumors
of the spine are rareof the spine are rare
especially of theespecially of the
cervical spine.cervical spine.
However it is quiteHowever it is quite
consideralbeconsideralbe
the incidencethe incidence
of metastasisof metastasis
A.B.CA.B.C
4. Benign tumors of the spineBenign tumors of the spine
The most common benign tumorsThe most common benign tumors
are:are:
– HemangiomaHemangioma
– OsteoblastomaOsteoblastoma
– Giant cell tumorGiant cell tumor
– ChondroblastomaChondroblastoma
– Osteoid osteomaOsteoid osteoma
Their incidence is estimated to beTheir incidence is estimated to be
11% – 14%11% – 14%
A lot of them remain asymptomaticA lot of them remain asymptomatic
and are diagnosed accidentallyand are diagnosed accidentally
Osteochondroma
5. Malignant tumors of the spineMalignant tumors of the spine
(primary and metastatic)(primary and metastatic)
The primary malignant tumors areThe primary malignant tumors are
rare in the spinerare in the spine
The most common are:The most common are:
– OsteosarcomaOsteosarcoma
– ChondroblastomaChondroblastoma
– Ewing’s sarcomaEwing’s sarcoma
– ChordomaChordoma
– LymphomaLymphoma
Ewing’s sarcoma
6. Are the most commonAre the most common
in the spinein the spine
The life expectancyThe life expectancy
contributescontributes
to the increasedto the increased
incidenceincidence
of spinal metastasesof spinal metastases
Breast metatstasis
Metastatic spinal tumorsMetastatic spinal tumors
8. The most common locationThe most common location
for skeletal metastasis:for skeletal metastasis:
• ThoracolumbarThoracolumbar
regionregion ~~ 70%70%
• Lumbar and sacralLumbar and sacral
spinespine ~~ 20%20%
• Cervical spineCervical spine ~~ 10%10%
Gilbert R.W. et al.
Ann. Neural. 1998 Stomach metastasisStomach metastasis
10. PAIN
Is the most
common
symptom related
to the existence
of a primary or
metastatic spinal
tumor
Breast metastasisBreast metastasis
11. The spinal pain may be due:The spinal pain may be due:
In destruction of the anatomicIn destruction of the anatomic
vertebral elements as a resultvertebral elements as a result
of metastasesof metastases
Resulting spinal instabilityResulting spinal instability
The pain is possible to occurThe pain is possible to occur
as a result of compression oras a result of compression or
infiltration of the spinalinfiltration of the spinal
cord – nerves fromcord – nerves from
neoplasmatic masses.neoplasmatic masses.
Stomach metastasisStomach metastasis
26. Factors for evaluationFactors for evaluation::
– The biology of the tumorThe biology of the tumor
– The locationThe location
– The painThe pain
– The neurologic deficitThe neurologic deficit
– The spinal instabilityThe spinal instability
– Life expectancyLife expectancy
– Overall condition of the patientOverall condition of the patient
Aboulafia A. Levine A., OKU Spine 2, 2004
27. 1. Spinal instability
2. Pain resistible to
conservative treatment
(radiotherapy –
chemotherapy)
3. Incomplete neurologic
deficit resistible to any
type of conservative
treatment
4. Rapid deterioration of the
neurologic deficit
Indications for operative treatmentIndications for operative treatment
30. Tomita’s staging classification systemTomita’s staging classification system
for the primary tumors of the spinefor the primary tumors of the spine
Intra-compartmental Extra-compartmental Multiple skip
lesion
Type 1
Type 2
Type 3
Type 4
Type 5
Type 6
Type 7
Site
(1 or 2 or 3)
Anterior or posterior
Lesion in situ
Site
(1 +2 or 3 + 2)
Extension to pedicle
Site
(1 +2 +r 3)
Anterio-posterior
development
(any site + 4)
Epidural extension
(any site + 5)
Paravertebral
development
Involvement to
adjacent vertbra
Tomita T, et al, Spine 2001
31. ChondrosarcomaChondrosarcoma
The most commonThe most common
malignant tumor ofmalignant tumor of
the bone in thethe bone in the
spinespine
7% - 12% of all7% - 12% of all
spine tumorsspine tumors
M. Riz.
F 41
15-6-1997
34. Tokuhashi
scoring system
Tomita
surgical staging
Karnofsky
performance status
scale definitions
rating (%) criteria
Methods of evaluation
E. Kar.
F 52
4-6-1991
35. Tokuhashi’sTokuhashi’s Evaluation System forEvaluation System for
prognosis of metastatic spinal tumorsprognosis of metastatic spinal tumors
SymptomsSymptoms 00 11 22
General conditionGeneral condition
performance statusperformance status
PoorPoor
(PS 10% to 40%)(PS 10% to 40%)
ModerateModerate
(50% to 70%)(50% to 70%)
GoodGood
(80% to 100%)(80% to 100%)
No of extraspinalNo of extraspinal
skeletal metastasesskeletal metastases
>3>3 1 to 21 to 2 00
Metastases toMetastases to
internal organsinternal organs
UnremovableUnremovable RemovableRemovable No metastasesNo metastases
Primary site of tumorPrimary site of tumor Lung stomachLung stomach Kidney liver uterusKidney liver uterus
unknownunknown
Thyroid prostateThyroid prostate
breast rectumbreast rectum
Number ofNumber of
metastasesmetastases
>3>3 22 11
Spinal cord palsySpinal cord palsy CompleteComplete IncompleteIncomplete NoneNone
Tokuhashi, Y. et al, Spine 1990
Total score versus survival period:
9 to 12 points > 12 months survival
0 to 5 points < 3 months survival
36. These criteria allow the definition of a
pre-operative strategy and therefore
considerable variability in the choice of
treatment ranging:
• excisional operation should be performed
on those who scored above 9 points
• a palliative operation should be performed
on those who scored under 5 points
Tokuhashi Y. et al.
Spine 1990
37. Simpler system of preoperative
evaluation based on only three
parameters:
• the degree of malignacy
• the presence of visceral metastases
• the presence of bony metastases.
Tomita K. et al.
Spine 2001
Bauer H. et al.
Spine 2002
38. Tomita’s classification systemTomita’s classification system
Intra-compartmental Extra-compartmental Multiple skip
lesion
Type 1
Type 2
Type 3
Type 4
Type 5
Type 6
Type 7
Site
(1 or 2 or 3)
Anterior or posterior
Lesion in situ
Site
(1 +2 or 3 + 2)
Extension to pedicle
Site
(1 +2 +r 3)
Anterio-posterior
development
(any site + 4)
Epidural extension
(any site + 5)
Paravertebral
development
Involvement to
adjacent vertbra
Tomita T, et al, Spine 2001
39.
40. Palliative treatment, generally
produces modest results, but
contributes greatly to the quality
of life.
Moreover, it is reasonable to use
palliative means when life
expectancy is only:
4 to 15 months.
Wise J.F. et al Spine 1999.
Bouer H. et al. Spine 2002.
Palliative treatmentPalliative treatment
Pneumon’ s metastasis
Posterior
decompression & stabilization
42. Vast majority can be managedVast majority can be managed
with dorsal fixationwith dorsal fixation
Rarely is ventral decompressionRarely is ventral decompression
indicated or necessaryindicated or necessary
Preoperative spinal fracturePreoperative spinal fracture
reduction may be attemptedreduction may be attempted
with awake tractionwith awake traction
Ventral decompression may beVentral decompression may be
indicated to decompressindicated to decompress
significant ventral tumor causingsignificant ventral tumor causing
persistent spinal cordpersistent spinal cord
compressioncompression
Moulopoulos et al, Clin Imaging 1997
Poynton Asley et al, Cancer in the spine, 2006
Atlanto-axial metastaticAtlanto-axial metastatic
spinal tumorsspinal tumors
44. a. Posterior decompression and
Occipitocervical stabilization
b. Post-operative adjuvant
chemotherapy - radiotherapy
N(-)
N(-)
3 yrs pop
A. St
F-84 yrs
14-7-2011
45. Metastastic disease of theMetastastic disease of the
subaxial cervical spine issubaxial cervical spine is
more common than themore common than the
atlanto-axial spineatlanto-axial spine
As with atlanto-axial tumorsAs with atlanto-axial tumors
the majority of the patientsthe majority of the patients
can be managed withcan be managed with
radiation therapyradiation therapy
Sub-axial cervical spineSub-axial cervical spine
metastatic tumorsmetastatic tumors
57. is treated successfully
only by operative
procedure
Spinal instability due to
bone destruction
Breast’s metastasisBreast’s metastasis
C3
58. Prosthetic replacementProsthetic replacement
is indicated in case ofis indicated in case of
vertebral destructionvertebral destruction
at one or twoat one or two
consecutive vertebraeconsecutive vertebrae
Benign spinal tumorsBenign spinal tumors
Malignant primary spinalMalignant primary spinal
tumorstumors
Selected cases ofSelected cases of
metastatic spinal tumorsmetastatic spinal tumors
60. Anterior vertebral replacement andAnterior vertebral replacement and
anterior – posterior stabilizationanterior – posterior stabilization
1. Is indicated
in excessively
unstable spine
and
2. It gives the best
overall results