نتایج جستجو برای: parosteal osteosarcoma

تعداد نتایج: 11824  

Journal: :Journal of Orthopedics, Traumatology and Rehabilitation 2018

Journal: :Proceedings 2012
L Michael Kershen William G Schucany Nathan F Gilbert

Bizarre parosteal osteochondromatous proliferation is a rare benign condition of locally aggressive and often recurrent osteochondromatous exostosis arising from the bony cortex. We present a case of a patient who presented with this lesion in her tibia, focusing on imaging findings. Because of the lack of information on the disease's natural history, etiology, and clinical course, a multidisci...

Journal: :The Journal of bone and joint surgery. American volume 2015
M P A Bus J A M Bramer G R Schaap H W B Schreuder P C Jutte I C M van der Geest M A J van de Sande P D S Dijkstra

BACKGROUND Selected primary tumors of the long bones can be adequately treated with hemicortical resection, allowing for optimal function without compromising the oncological outcome. Allografts can be used to reconstruct the defect. As there is a lack of studies of larger populations with sufficient follow-up, little is known about the outcomes of these procedures. METHODS In this nationwide...

2010
Dawood Jafari Hooman Shariatzadeh Khodamorad Jamshidi

Bizarre parosteal osteochondromatous proliferation (BPOP), also known as Nora's lesion is a rare osteocartilaginous lesion composed of a disorganized mixture of cartilage, bone, and fibrous tissue. In this article we report a case of BPOP arising on the proximal and middle phalanx of ring finger in a 31 year-old woman. The clinical, radiographic, MR imaging and histopathologic findings of it ar...

Journal: :iranian biomedical journal 0
اسماعیل بابایی esmaeil babaei سیدجواد مولی seyed javad mowla شمس شریعت تربقان shams shariat torbaghan مجتبی عمادی بایگی mojtaba emadi bayegi

osteosarcoma is a relatively uncommon malignancy however, it is the most common form of primary malignant bone tumors in human. diagnosis and prognosis of patients with osteosarcoma is limited to clinico-radiopathological parameters, whereas molecular markers of tumor aggression have been poorly identified. survivin, an inhibitor of apoptosis (iap), is unique for its expression in human tumors ...

Journal: :iranian journal of radiology 0
wang liuhong department of radiology, the second affiliated hospital, zhejiang university, school of medicine, hangzhou, china zhang minming department of radiology, the second affiliated hospital, zhejiang university, school of medicine, hangzhou, china; department of radiology, the second affiliated hospital, zhejiang university, school of medicine, hangzhou, china , +86-57187315255

hereby we report a case of well-differentiated intraosseous osteosarcoma in the sacrum. a 32-year-old woman was admitted to our hospital with a low echo-level mass in the pelvis searched by ultrasound in a routine physical examination. radiographically, the mass was misdiagnosed as a benign bony tumor originating from the sacrum. the tumor was completely resected and pathological diagnosis was ...

Journal: :acta medica iranica 0
m. eslami f. baghaee m. alaeddini

it is sometimes difficult to recognize a jaw lesion as osteosarcoma, ossifying fibroma or ‎fibrous dysplasia in routine hematoxylin and ‎eosin staining and a more accurate technique is needed to differentiate these ‎lesions. ‎many studies have shown the potential usefulness of silver-stained nucleolar organizer region (agnor) parameters for the diagnosis of various neoplasms. this study was car...

Esmaeil Babaei, Mojtaba Emadi Bayegi, seyed javad Mowla, Shams Shariat Torbaghan,

Osteosarcoma is a relatively uncommon malignancy however, it is the most common form of primary malignant bone tumors in human. Diagnosis and prognosis of patients with osteosarcoma is limited to clinico-radiopathological parameters, whereas molecular markers of tumor aggression have been poorly identified. Survivin, an inhibitor of apoptosis (IAP), is unique for its expression in human tumors ...

Journal: :International Journal of Orthopaedics Sciences 2023

Giant cell-rich osteosarcoma is an extremely rare variant of conventional osteosarcoma. It accounts for only 1%-3%. undifferentiated high-grade sarcoma with numerous osteoclast-like giant cells. also contains variable amount tumor osteoid. This article aims to present a case involving the right knee joint in young man.

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