Results for Bone Chip Transplantation after Curettage of Benign Bone Tumors
نویسندگان
چکیده
منابع مشابه
Extended Curettage for Benign Bone Lesions
Benign bone lesions present a unique challenge to the practicing orthopaedist. They are a not uncommon problem that often present in the pediatric or young adult population. The most common diagnoses include giant cell tumor of bone, aneurysmal bone cysts, unicameral (simple) bone cysts, metaphyseal fibrous defects, and fibrous dysplasia. Appropriate surgical intervention must balance acceptabl...
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Background & Objective: Bone marrow stromal cells (BMSCs) are multipotent stem cells that can proliferate and differentiate into osteogenic cells . T his study aimed to investigate the effects of BMSC transplantation for the repair of bone defects in the rat. Materials & Methods : Twenty-eight male adult rats were divided into 4 groups. Group 1 ( control group) received no treatment after the...
متن کاملBone Transport for Reconstruction in Benign Bone Tumors
BACKGROUND The aim of this study was to assess the results of using the Ilizarov apparatus to transport bones in the treatment of benign bone tumors. METHODS Seven patients (six males and one female) with benign bone tumors were treated by bone transport with an Ilizarov apparatus at our institution. Their mean age at surgery was 14.4 years (range, 4.8 to 36.9 years). The histological diagnos...
متن کاملSurgical consideration for benign bone tumors.
BACKGROUND The surgical management of symptomatic benign bone tumor has been described in various manners in medical literature. However, there are few published reports on the presentation and surgical management of benign bone tumors in black African patients. OBJECTIVES To determine the pattern of presentation of benign bone tumors and evaluate the common indications for surgery in a Niger...
متن کاملSlide Seminar - Part I: Benign Bone Tumors
FD is a genetic non-inherited condition caused by missense mutation in the gene GNAS1 on chromosome 20, that encodes the alpha subunit of the stimulatory G protein-coupled receptor, Gsα. The activating mutations occur post-zygotically, replacing the arginine residue amino acid with either a cystein or a histidine amino acid. The mutation selectively inhibits GTPase activity, resulting in consti...
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ژورنال
عنوان ژورنال: Orthopedics & Traumatology
سال: 1957
ISSN: 1349-4333,0037-1033
DOI: 10.5035/nishiseisai.7.75