نتایج جستجو برای: Bone neoplasm
تعداد نتایج: 473464 فیلتر نتایج به سال:
abstract patella is a relative uncommon site for chondroblastoma. most of cases of chondroblastoma in patella reported in literature are treated with patellectomy. we treated a large chondroblastic lesion in patella of an 18- year-old male with curettage, burring & bone graft and the result was satisfactory after 3 years post operation.
desmoplastic fibroma (df) is a rare and locally aggressive intraosseous tumor with unknown etiology. the mandible is the common site of involvement in the maxillofacial region. however, it is believed that df can arise in any bone of the body. a wide age distribution has been reported for df occurrence, extending from birth to the sixth decade of life, with a peak incidence at 10 to 19 years of...
normal 0 false false false en-us x-none ar-sa microsoftinternetexplorer4 there are a few case series of giant cell tumor (gct) in the spine and sacrum. gct in the thoracic vertebrae is even more exceptional in the medical literature. in this article we report a gct in a 25-year-old male who presented with progressive back pain and dyspnea. on contrast-enhanced multidetector computer tomography,...
Chloroma or granulocytic sarcoma (GS) is a malignant neoplasm of myeloid lineage that occur in a variety of anatomic sites other than the bone marrow including soft tissue, bone, lymph node, nasal fossa, skin and sometime in the orbit. In the subconjunctiva it is rarely reported. A 4-year-old girl with a history of treated acute myelogenous leukemia was referred to Farabi Eye Hospital, Tehra...
Langerhans cell histiocytosis (LCH) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. The major pathological features of LCH are expression of CD1a and S100 as well as Birbeck granules. Its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...
chloroma or granulocytic sarcoma (gs) is a malignant neoplasm of myeloid lineage that occur in a variety of anatomic sites other than the bone marrow including soft tissue, bone, lymph node, nasal fossa, skin and sometime in the orbit. in the subconjunctiva it is rarely reported. a 4-year-old girl with a history of treated acute myelogenous leukemia was referred to farabi eye hospital, tehran, ...
Osteoid osteoma (OO) is a benign osteogenic lesion that is extremely rare in jaws. It is characterized by proliferation of either cancellous or compact bone and can be central, peripheral or extraskeletal. Pain is a distinctive feature of this lesion accompanied by vasomotor disturbances, which occur long before radiographic and histopathology findings manifest. Here, we present a rare case rep...
langerhans cell histiocytosis (lch) is a rare neoplasm defined as the proliferation of bone marrow langerhans cells, which is a kind of dendritic cells. the major pathological features of lch are expression of cd1a and s100 as well as birbeck granules. its presentation can differ from a mild bone lesion to a multi-systemic evolved malignant neoplasm; however, the latter outcome is almost rare. ...
Extramedullary plasmacytoma (EMP) is a rare neoplasm of soft tissue which usually arises in the respiratory tract, nasal cavity, sinuses and nasopharynx. Multiple extramedullary plasmacytomas are extremely rare, especially those that are not associated with multiple myeloma.We describe multiple primary EMP in a 37 year old man, without involvement of bone or bone marrow. EMP usually has a ...
Cemento-ossifying fibroma is a rare benign fibro-osseous neoplasm commonly involving the jaws majority of lesions occur in mandible bone. It can be discovered as an incidental finding radiological imaging. Symptomatic patients are presented with slowly growing mass bone and attain large size passage time. cause facial deformity if left untreated. We present such case right hemi-mandible bone, i...
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