low back pain/sarcoma

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Myeloid Sarcoma Presenting as Low Back Pain in the Pediatric Emergency Department.

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BACKGROUND Low back pain is a common symptom in the pediatric population; approximately half of all children present with at least one episode of low back pain. The majority of cases are due to nonspecific causes such as musculoskeletal trauma with spontaneous regression. On some occasions, however,

A rare synovial sarcoma of the spine in the thoracic vertebral body.

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BACKGROUND Synovial sarcomas of the spine are very rare, most rare of which was occurring in the thoracic vertebral body. The diagnosis of synovial sarcomas was very difficult. It depends on the radiological examination, immunohistochemical examination and gene examination. The best treatment to

A case of oesophageal cancer with low back pain: the accidental finding of skeletal muscle metastasis.

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Skeletal muscle metastasis is a very rare event in patients with oesophageal cancer. We herein report and discuss a case of a 65 years old man with history of gastro-esophageal reflux disease referred to our department for pyrosis associated to persistent low back pain. Oesophageal endoscopy and

Total en bloc spondylectomy of L3 vertebra for histiocytic sarcoma.

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This article describes a rare malignant spinal tumor successfully treated with total en bloc spondylectomy via a posterior approach. The purpose of this study was to emphasize the occurrence of primary histiocytic sarcoma in the lumbar spine. Histiocytic sarcomas are rare, malignant neoplasms of the

Synchronic renal cell carcinoma associated with fibromixoid sarcoma: A rare finding.

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Renal cell carcinoma comprises over 90% of renal cancers, thus, it is the most common form of renal neoplasia. This carcinoma can often present itself in a variable fashion, ranging from incidentalomas to metastatic diseases. Furthermore, the most common metastasis associated with this

Primary intramedullary spinal sarcoma : a case report and review of the current literatures.

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Primary central nervous system (CNS) sarcomas are exceedingly rare, and, to the best of our knowledge, there has not yet been a report of intramedullary sarcoma. Here, we report a primary intradural intramedullary sarcoma of the spinal cord in a four-year-old boy who presented with low back pain and

A case of spindle cell dominant histiocytic sarcoma showing a complete remission after first-line chemotherapy with doxorubicin and ifosfamide

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Histiocytic sarcoma (HS), an extremely rare malignancy, usually follows a progressive time course, and patients die within two years of diagnosis. At present, there is no consensus for effective chemotherapy.We report the case of a 54-year-old man who presented with low back pain and left hip joint

Metastatic synovial sarcoma to the left atrium. A management dilemma.

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We present a rare case of synovial sarcoma with minimal symptoms that metastasized and threatened to embolize the heart in a 26-year-old male admitted to our hospital for evaluation of low back pain. The tumor made a direct extension to the left atrium and moved freely in the left ventricle outflow

Epithelioid sarcoma of the spine: case report and literature review.

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Epithelioid sarcomas are rare mesenchymal neoplasms mainly arising in the limbs of young adults. We report the case of a 24-year-old male presenting low back pain radiating to both lower limbs, constipation and urinary retention. The MRI scan showed an intraspinal lesion extending from L4 to S2.

Erythroblastic sarcoma, an extremely rare variant of myeloid sarcoma.

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A 79-year-old man was admitted to the hospital because of a 20-lb weight loss, low back pain, and leg weakness. He had a 1-year history of fibrotic myelodysplasia, possibly therapy related, with a highly complex chromosome karyotype. Radiologic evaluation showed extensive destructive bone lesions,

Comparative study on low back pain misdiagnosed as spondyloarthropathy.

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This study aims to investigate features of different diseases with low back pain misdiagnosed as spondyloarthropathy so as to improve the accuracy of diagnosis for spondyloarthropathy. The clinical and laboratory data of 24 cases misdiagnosed as spondyloarthropathy in recent 3 years were

Primary Ewing sarcoma of the spine mimicking a psoas abscess secondary to spinal infection.

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METHODS A case of primary Ewing sarcoma of the lumbar spine is presented. OBJECTIVE To present and review a rare case of primary Ewing sarcoma of the lumbar spine that required differentiation from spinal infection. BACKGROUND Primary Ewing sarcoma originating from the spinal column is very rare.

Primary intradural extraosseous Ewing's sarcoma of the lumbar spine presenting with acute bleeding.

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We report the case of a 28-year-old female with primary extraosseous Ewing's sarcoma who presented initially with a low back pain and a right S1 radicular pain. Before scheduled surgical removal, she suddenly developed an unusual complication of an acute hemorrhage and an acute cauda equina

Primary spinal epidural Ewing sarcoma: a case report and review of the literature.

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Primary extraosseous Ewing sarcoma is a rare entity, especially in the spinal epidural site. Less than 20 cases have been reported in the literature. Here, we present a previously healthy 12-year-old boy who complained of low back pain, progressive gait disturbance and weakness of right lower

Radiation-recall myositis presenting as low-back pain (2010: 4b).

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We report on a patient with a history of Ewing sarcoma who underwent surgery and subsequent adjuvant chemotherapy and radiotherapy. He developed low-back pain 6 months after the end of the radiotherapy and during consolidation chemotherapy. Magnetic resonance imaging showed evidence of myositis

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