A locally aggressive, osteolytic neoplasm of the long bones, probably of epithelial origin and most often involving the TIBIA.
A disease of bone marked by thinning of the cortex by fibrous tissue containing bony spicules, producing pain, disability, and gradually increasing deformity. Only one bone may be involved (FIBROUS DYSPLASIA, MONOSTOTIC) or several (FIBROUS DYSPLASIA, POLYOSTOTIC).
An immature epithelial tumor of the JAW originating from the epithelial rests of Malassez or from other epithelial remnants of the ENAMEL from the developmental period. It is a slowly growing tumor, usually benign, but displays a marked propensity for invasive growth.
The second longest bone of the skeleton. It is located on the medial side of the lower leg, articulating with the FIBULA laterally, the TALUS distally, and the FEMUR proximally.
The bone of the lower leg lateral to and smaller than the tibia. In proportion to its length, it is the most slender of the long bones.
Tumors or cancer located in bone tissue or specific BONES.
A malignant tumor of the bone which always arises in the medullary tissue, occurring more often in cylindrical bones. The tumor occurs usually before the age of 20, about twice as frequently in males as in females.
A connective tissue neoplasm formed by proliferation of mesodermal cells; it is usually highly malignant.
A ubiquitous hnRNP protein found in the CELL NUCLEUS and the CYTOPLASM. Translocations that result in the formation of fusion proteins containing parts of RNA-binding protein EWS may play a role in neoplastic processes such as EWING SARCOMA.
A member of the c-ets family of transcription factors that is preferentially expressed in cells of hematopoietic lineages and vascular endothelial cells. It was originally identified as a protein that provides a retroviral integration site for integration of FRIEND MURINE LEUKEMIA VIRUS.
Neoplasms of whatever cell type or origin, occurring in the extraskeletal connective tissue framework of the body including the organs of locomotion and their various component structures, such as nerves, blood vessels, lymphatics, etc.
A malignant neoplasm arising from tenosynovial tissue of the joints and in synovial cells of tendons and bursae. The legs are the most common site, but the tumor can occur in the abdominal wall and other trunk muscles. There are two recognized types: the monophasic (characterized by sheaths of monotonous spindle cells) and the biphasic (characterized by slit-like spaces or clefts within the tumor, lined by cuboidal or tall columnar epithelial cells). These sarcomas occur most commonly in the second and fourth decades of life. (From Dorland, 27th ed; DeVita Jr et al., Cancer: Principles & Practice of Oncology, 3d ed, p1363)
Progressive restriction of the developmental potential and increasing specialization of function that leads to the formation of specialized cells, tissues, and organs.
Deformities of the SPINE characterized by abnormal bending or flexure in the vertebral column. They may be bending forward (KYPHOSIS), backward (LORDOSIS), or sideway (SCOLIOSIS).
A condition characterized by a series of interrelated digital symptoms and joint changes of the lesser digits and METATARSOPHALANGEAL JOINTS of the FOOT. The syndrome can include some or all of the following conditions: hammer toe, claw toe, mallet toe, overlapping fifth toe, curly toe, EXOSTOSIS; HYPEROSTOSIS; interdigital heloma, or contracted toe.
A synovial hinge connection formed between the bones of the FEMUR; TIBIA; and PATELLA.
Tumors or cancer located in muscle tissue or specific muscles. They are differentiated from NEOPLASMS, MUSCLE TISSUE which are neoplasms composed of skeletal, cardiac, or smooth muscle tissue, such as MYOSARCOMA or LEIOMYOMA.
An appreciable lateral deviation in the normally straight vertical line of the spine. (Dorland, 27th ed)
Injuries incurred during participation in competitive or non-competitive sports.
Alterations or deviations from normal shape or size which result in a disfigurement of the foot.
A focal malformation resembling a neoplasm, composed of an overgrowth of mature cells and tissues that normally occur in the affected area.
The simultaneous analysis of multiple samples of TISSUES or CELLS from BIOPSY or in vitro culture that have been arranged in an array format on slides or microchips.
The longest and largest bone of the skeleton, it is situated between the hip and the knee.
A sarcoma originating in bone-forming cells, affecting the ends of long bones. It is the most common and most malignant of sarcomas of the bones, and occurs chiefly among 10- to 25-year-old youths. (From Stedman, 25th ed)
A specialized CONNECTIVE TISSUE that is the main constituent of the SKELETON. The principle cellular component of bone is comprised of OSTEOBLASTS; OSTEOCYTES; and OSTEOCLASTS, while FIBRILLAR COLLAGENS and hydroxyapatite crystals form the BONE MATRIX.
A specialty concerned with the use of x-ray and other forms of radiant energy in the diagnosis and treatment of disease.
Examination of any part of the body for diagnostic purposes by means of X-RAYS or GAMMA RAYS, recording the image on a sensitized surface (such as photographic film).
The downward displacement of the cuspal or pointed end of the trileaflet AORTIC VALVE causing misalignment of the cusps. Severe valve distortion can cause leakage and allow the backflow of blood from the ASCENDING AORTA back into the LEFT VENTRICLE, leading to aortic regurgitation.
Reversible chemical reaction between a solid, often one of the ION EXCHANGE RESINS, and a fluid whereby ions may be exchanged from one substance to another. This technique is used in water purification, in research, and in industry.
An order of the Amphibia class which includes salamanders and newts. They are characterized by usually having slim bodies and tails, four limbs of about equal size (except in Sirenidae), and a reduction in skull bones.
Two populations of Zucker rats have been cited in research--the "fatty" or obese and the lean. The "fatty" rat (Rattus norvegicus) appeared as a spontaneous mutant. The obese condition appears to be due to a single recessive gene.
A growth differentiation factor that plays a role in the genesis of left-right asymmetry during vertebrate development. Evidence for this role is seen in MICE where loss of growth differentiation factor 1 function results in right-left isomerism of visceral organs. In HUMANS heterozygous loss of growth differentiation factor 1 function has been associated with CONGENITAL HEART DEFECTS and TRANSPOSITION OF GREAT VESSELS.
Nucleotides in which the base moiety is substituted with one or more sulfur atoms.
A DNA-dependent RNA polymerase present in bacterial, plant, and animal cells. It functions in the nucleoplasmic structure where it transcribes DNA into RNA. It has specific requirements for cations and salt and has shown an intermediate sensitivity to alpha-amanitin in comparison to RNA polymerase I and II. EC 2.7.7.6.
The continuous turnover of BONE MATRIX and mineral that involves first an increase in BONE RESORPTION (osteoclastic activity) and later, reactive BONE FORMATION (osteoblastic activity). The process of bone remodeling takes place in the adult skeleton at discrete foci. The process ensures the mechanical integrity of the skeleton throughout life and plays an important role in calcium HOMEOSTASIS. An imbalance in the regulation of bone remodeling's two contrasting events, bone resorption and bone formation, results in many of the metabolic bone diseases, such as OSTEOPOROSIS.
The amount of mineral per square centimeter of BONE. This is the definition used in clinical practice. Actual bone density would be expressed in grams per milliliter. It is most frequently measured by X-RAY ABSORPTIOMETRY or TOMOGRAPHY, X RAY COMPUTED. Bone density is an important predictor for OSTEOPOROSIS.
Component of the NATIONAL INSTITUTES OF HEALTH. Through basic and clinical biomedical research and training, it conducts and supports research with the objective of cancer prevention, early stage identification and elimination. This Institute was established in 1937.
Bone loss due to osteoclastic activity.
The soft tissue filling the cavities of bones. Bone marrow exists in two types, yellow and red. Yellow marrow is found in the large cavities of large bones and consists mostly of fat cells and a few primitive blood cells. Red marrow is a hematopoietic tissue and is the site of production of erythrocytes and granular leukocytes. Bone marrow is made up of a framework of connective tissue containing branching fibers with the frame being filled with marrow cells.

Allograft reconstruction for bone sarcoma of the tibia in the growing child. (1/12)

The outcome of tibial allograft reconstruction after resection of a tumour is inconsistent and has a high rate of failure. There are few reports on the use of tibial allografts in children with open growth plates. We performed 21 allograft reconstructions (16 osteoarticular, five intercalary) in 19 consecutive patients between seven and 17 years of age. Two had Ewing's sarcoma, one an adamantinoma and 16 osteosarcoma, one with multifocal disease. Five patients have died; the other 14 were free from disease at the time of follow-up. Six surviving patients (eight allograft reconstructions) continue to have good or excellent function at a mean of 59 months (14 to 132). One patient has poor function at 31 months. The other seven patients have a good or excellent function after additional procedures including exchange of the allograft and resurfacing or revision to an endoprosthesis at a mean of 101 months (43 to 198). The additional operations were performed at a mean of 47 months (20 to 84) after the first reconstruction. With the use of allograft reconstruction in growing children, joints and growth plates may be preserved, at least partially. Although our results remain inconsistent, tibial allograft reconstruction in selected patients may restore complete and durable function of the limb.  (+info)

A classic adamantinoma arising from osteofibrous dysplasia-like adamantinoma in the lower leg: a case report and review of the literature. (2/12)

Adamantinoma is known as a low-grade malignant biphasic tumor. Classic adamantinoma is in general characterized by admixture of both epithelial and osteofibrous components that are associated with various proportions and differentiation patterns. Osteofibrous dysplasia (OFD) is a self-limited benign fibro-osseous lesion of bone during infancy and childhood. OFD-like adamantinoma is characterized by predominance of osteofibrous tissues, in which small groups of epithelial cells are only detected by careful search or immunohistochemistry. There have been controversies as to the potential correlation among OFD, OFD-like adamantinoma and classic adamantinoma. We report an unusual case of adamantinoma arising in the tibia, with an extensive review of the literature. The present findings suggest a direct correlation between OFD-like adamantinoma and classic adamantinoma. At the age of 12 years, the tibial biopsy lesion was diagnosed as OFD. At the age of 23, the lesion became larger and more destructive on x-ray films. The biopsy lesion was diagnosed as classic adamantinoma. Wide excision was performed. The primary lesion was retrospectively diagnosed as OFD-like adamantinoma because of presence of keratin-positive epithelial cells within the stroma. At five years after surgery, the patient was free from recurrence or metastasis. The retrospective histological findings of OFD-like adamantinoma in the original biopsy and of a classic adamantinoma in all sections of the later resection specimen raised the possibility of an unusual progression of OFD-like adamantinoma to a classic adamantinoma. The present case and the literature review suggest that an OFD-like adamantinoma may be a precursor lesion of classic adamantinoma. Therefore, the possibility of progression of OFD-like adamantinoma to a classic adamantinoma should be kept in mind, particularly when the destructive changes are seen radiologically.  (+info)

Osteofibrous dysplasia of the tibia. Is there a need for a radical surgical approach? (3/12)

Osteofibrous dysplasia is an unusual developmental condition of childhood, which almost exclusively affects the tibia. It is thought to follow a slowly progressive course and to stabilise after skeletal maturity. The possible link with adamantinoma is controversial and some authors believe that they are part of one histological process. We retrospectively reviewed 16 patients who were diagnosed as having osteofibrous dysplasia initially or on the final histological examination. Their management was diverse, depending on the severity of symptoms and the extent of the lesion. Definitive (extraperiosteal) surgery was localised "shark-bite" excision for small lesions in five patients. Extensive lesions were treated by segmental excision and fibular autograft in six patients, external fixation and bone transport in four and proximal tibial replacement in one. One patient who had a fibular autograft required further excision and bone transport for recurrence. Six initially underwent curettage and all had recurrence. There were no recurrences after localised extraperiosteal excision or bone transport. There were three confirmed cases of adamantinoma. The relevant literature is reviewed. We recommend extraperiosteal excision in all cases of osteofibrous dysplasia, with segmental excision and reconstruction in more extensive lesions.  (+info)

Fibular osteoadiposal flap for treatment of tibial adamantinoma: a case report. (4/12)

We treated a case with left tibial adamantinoma by use of a contralateral fibular osteoadiposal flap. The donor site of conventional fibular osteocutaneous flap must be covered with a skin graft because if we close the donor skin defect directly, compartment syndrome might occur. We were able to close the donor skin defect because this combined type flap included only a small monitoring skin paddle. We present herein the utility of the osteoadiposal flap and show the value of a skin-sparing approach with a minimal aesthetic defect.  (+info)

Preliminary report of expression of bax in oral cavity pathologies. (5/12)

Bax is considered one of major effectors of apoptosis--programmed cell death. Immunohistochemical analysis of in vitro patterns of bax expression was mostly investigated in mammalian cell lines and tissues. The present study is the first in vivo molecular analysis of bax expression in oral cavity pathologies. The study population consisted of 45 patients with hyperplasia, neoplasm in situ malignancy, and carcinoma. Biopsies were taken from incision line, tumour section, and healthy tissue. bax expression was investigated depending on the site of biopsy material sampling and final histopathology result. No statistically significant difference was demonstrated in bax expression between four hyperplasia subgroups. However, statistically significant differences in bax expression were found between the three basic study groups (P = 0.001). Statistically significant differences in bax expression were demonstrated depending on tissue collection site (P = 0.0002). We conclude that differences in bax expression may play a role in the pathogenesis of neoplastic disease.  (+info)

Adamantinoma of the tibia with late skeletal metastasis: an unusual presentation. (6/12)

Adamantinoma is a rare tumour of long bones that occurs most commonly in the tibia. Its pathogenesis is unknown. It is locally aggressive and recurrences are common after resection. Metastases have been reported in 10% to 20% of cases, most commonly in the lungs and rarely in the lymph nodes. We report a patient who developed a skeletal metastasis four years after resection of the primary tumour. There was no evidence of recurrence at the primary site or of secondary deposits in the lungs.  (+info)

Treatment of osteofibrous dysplasia and associated lesions. (7/12)

PURPOSE: To report long term treatment outcomes of osteofibrous dysplasia and association with adamantinoma. PATIENTS AND METHODS: From January 1984 to July 2001, 14 patients with osteofibrous dysplasia were followed for an average of 108 months (78 to 260 months). Our patient group consisted of 6 men and 8 women, with a mean age of 13.9 years (2 to 65 years). We reviewed the clinical and pathological features of all 14 patients. RESULTS: Thirteen patients had a lesion in the tibia, while one patient had lesions in both the tibia and the fibula. Initial treatments were observation after biopsy (6 patients), curettage with or without a bone graft (3 patients), resection followed by a free vascularized fibular bone graft (4 patients), or resection and regeneration with the Ilizarov external fixation (1 patient). Curettage was performed on 6 patients due to recurrence or progression after the initial treatment. Among these patients, one was diagnosed with AD from the biopsy of the recurrent lesion. This patient was further treated by segmental resection and pasteurization. After the initial pathology slides of the 13 patients were reviewed with immunohistochemical cytokeratin staining, one patient diagnosis was changed from osteofibrous dysplasia to osteofibrous dysplasia-like adamantinoma. CONCLUSION: Some patients with osteofibrous dysplasia require close observation because of the high association risk between osteofibrous dysplasia and adamantinoma, Immunohistochemical staining may be helpful in differentiating these two diagnoses.  (+info)

Analysis of stromal cells in osteofibrous dysplasia and adamantinoma of long bones. (8/12)

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MalaCards based summary : Adamantinoma of Long Bones, also known as long bone adamantinoma, is related to tibial adamantinoma and biphasic synovial sarcoma. An important gene associated with Adamantinoma of Long Bones is EGF (Epidermal Growth Factor), and among its related pathways/superpathways are Neural Stem Cell Differentiation Pathways and Lineage-specific Markers and Lung fibrosis. Affiliated tissues include long bones, bone and eye, and related phenotypes are neoplasm and pathologic fracture ...
TY - JOUR. T1 - Adamantinoma of the distal femur diagnosed 5 years after initial surgery. T2 - A case report. AU - Cao, Kai. AU - Susa, Michiro. AU - Watanabe, Itsuo. AU - Nishimoto, Kazumasa. AU - Horiuchi, Keisuke. AU - Sasaki, Aya. AU - Hayashi, Yuichiro. AU - Emoto, Katsura. AU - Kameyama, Kaori. AU - Nakamura, Masaya. AU - Matsumoto, Morio. AU - Morioka, Hideo. PY - 2016/6/23. Y1 - 2016/6/23. N2 - Background: Adamantinoma arising in the femur is extremely rare. We report a case of an adamantinoma occurring in the right medial femoral condyle that was diagnosed 5 years after the primary surgery. Case presentation: A 74-year-old Asian woman first complained of right knee pain without any cause. Radiographs demonstrated a 4×4.5 cm osteolytic lesion in her medial femoral condyle. Magnetic resonance imaging revealed a lesion which showed low signal on both T1 and T2-weighted image, and enhanced signal with gadolinium contrast administration. She underwent a wide resection of the lesion and was ...
TY - JOUR. T1 - Frequent immunoexpression of TGF-β1, FGF-2 and BMP-2 in fibroblast-like cells in osteofibrous dysplasia. AU - Sakamoto, Akio. AU - Oda, Yoshinao. AU - Iwamoto, Yukihide. AU - Tsuneyoshi, Masazumi. PY - 2007/3. Y1 - 2007/3. N2 - Osteofibrous dysplasia (OFD) and fibrous dysplasia (FD) are both benign bone lesions which comprise the proliferation of fibroblast-like cells with bone formation, and these fibroblast-like cells have the phenotype of osteoprogenitor cells. The roentgenograph of OFD shows a heterogeneous osteolytic lesion with surrounding osteosclerosis, whereas FD is typically characterized by a rather homogeneous osteolytic lesion, or ground-glass appearance, with a smaller amount of surrounding osteosclerosis. Growth factors of transforming growth factor-β1 (TGF-β1), fibroblast growth factor-2 (FGF-2) and bone morphogenetic protein-2 (BMP-2) modulate bone differentiation. Expression of these growth factors was examined in the fibroblast-like cells of 16 cases of ...
Adamantinoma usually presents as an intraosseous, intracortical stage I-A sarcoma.. This low-grade, slowly-growing malignancy metastasizes in about 20 percent of cases by both hematogenous and lymphatic routes to other parts of the body, usually to the lungs or nearby lymph nodes. Of these cases, about 15 percent of the patients die.. Young females seem to be at the highest risk for early demise with the average age of death being 33 years compared to 48 years for men.. ...
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Memorial Sloan Kettering surgeon Nicola Fabbri has 20 years of experience in treating musculoskeletal cancers, including osteosarcoma, Ewing Sarcoma, chondrosarcoma, soft tissue sarcomas, giant-cell tumor, chordoma, adamantinoma, osteofibrous dysplasia, angiosarcoma, and other vascular tumors.
Poster: ECR 2015 / B-0912 / Can ultrasound replace MRI in assessment of nerve entrapment in osteofibrous tunnels in the upper extremity by: A. Abdel Maguid, Y. M. Tohamey, T. Taymour, L. Adel; Cairo/EG
Ameloblastoma (from the early English word amel, meaning enamel + the Greek word blastos, meaning germ) is a rare, benign or cancerous tumor of odontogenic epithelium (ameloblasts, or outside portion, of the teeth during development) much more commonly appearing in the lower jaw than the upper jaw. It was recognized in 1827 by Cusack. This type of odontogenic neoplasm was designated as an adamantinoma in 1885 by the French physician Louis-Charles Malassez. It was finally renamed to the modern name ameloblastoma in 1930 by Ivey and Churchill. While these tumors are rarely malignant or metastatic (that is, they rarely spread to other parts of the body), and progress slowly, the resulting lesions can cause severe abnormalities of the face and jaw. Additionally, because abnormal cell growth easily infiltrates and destroys surrounding bony tissues, wide surgical excision is required to treat this disorder. If an aggressive tumor is left untreated, it can obstruct the nasal and oral airways making it ...
Looking for odontogenic epithelioma? Find out information about odontogenic epithelioma. An epithelial tumor associated with the enamel organ; cells of basal layers resemble the ameloblast. Also known as adamantinoma Explanation of odontogenic epithelioma
Abdominal Aortic Aneurysm Imaging Abdominal Aortic Aneurysm Rupture Imaging Acalculous Cholecystitis Imaging Acetabulum Fracture Imaging Achalasia Imaging Achondroplasia Imaging Acquired Temporal-Bone Cholesteatoma Imaging Acute Cholecystitis Imaging Acute Epiglottitis Imaging Acute Myocardial Infarct Imaging Acute Obstructive Uropathy Imaging Acute Pancreatitis Imaging Acute Pulmonary Embolism (Helical CT) Acute Pyogenic Osteomyelitis Imaging Adamantinoma Imaging Adenomyomatosis Imaging Adenomyosis Imaging…
Tropes relating to the cast of Tales of Vesperia. BE WARNED THAT NOT ALL SPOILERS ARE MARKED. Brave Vesperia Brave Vesperia is the Guild formed by Karol, …
Ossifying fibromas are benign bone lesions that should be differentiated from non-ossifying fibromas and fibrous dysplasia. Osteofibrous dysplasia is considered as a separate pathological entity in view of its different presentation and treatment...
This type of odontogenic neoplasm was designated as an adamantinoma in 1885 by the French physician Louis-Charles Malassez. It ...
... and adamantinoma. BCRT was initially a parents' group started in September 2004. Five families who had lost children to ...
"A classic adamantinoma arising from osteofibrous dysplasia-like adamantinoma in the lower leg: a case report and review of the ... Several authors have related this non-neoplastic lesion to adamantinoma - a tumor involving subcutaneous long bones - stating ...
... adamantinoma MeSH C05.116.231.343 - femoral neoplasms MeSH C05.116.231.754 - skull neoplasms MeSH C05.116.231.754.450 - jaw ...
... adamantinoma MeSH C04.588.149.276 - femoral neoplasms MeSH C04.588.149.721 - skull neoplasms MeSH C04.588.149.721.450 - jaw ...
... a bulky hydrocarbon Adamantinoma, a form of bone cancer Adamantium, a fictional metal alloy appearing in comic books published ...
NOS Adamantinoma, NOS (except of long bones M9261/3) M9310/3 Ameloblastoma, malignant Adamantinoma, NOS (except of long bones ... malignant M9260/3 Ewing's sarcoma/tumor M9261/3 Adamantinoma of long bones M9262/0 Ossifying fibroma Fibro-osteoma Osteofibroma ...
Hemangioendothelioma Angiosarcoma Fibrosarcoma/myofibrosarcoma Chordoma Adamantinoma Other: Liposarcoma Leiomyosarcoma ...
Adamantinoma - Adhesive capsulitis of shoulder - Advanced trauma life support - Ainhum - Akin osteotomy - Albers-Schonberg ...
"A classic adamantinoma arising from osteofibrous dysplasia-like adamantinoma in the lower leg: a case report and review of the ... Benign osteofibrous dysplasia may be a precursor of adamantinoma or a regressive phase of adamantinoma. Histologically, islands ... Adamantinoma (from the Greek word adamantinos, meaning "very hard") is a rare bone cancer, making up less than 1% of all bone ... "Adamantinoma: Overview - eMedicine". Archived from the original on 25 December 2008. Retrieved 2009-01-04. Fischer B. Uber ein ...
Adamantinoma. *Adams-Nance syndrome. *Adams-Oliver syndrome. *Adams-Stokes syndrome. *Addison's disease ...
Pain may be relieved by nonsteroidal anti-inflammatory drugs.. Treatment varies based on the health of the patient. If he/she is otherwise healthy and is not significantly bothered by the pain, the tumor is treated symptomatically with anti-inflammatories. If this therapy fails or the location of the tumor could lead to growth disturbances, scoliosis, or osteoarthritis, surgical or percutaneous ablation may be considered.[10] If surgery is preferred, the individual may be referred to a podiatrist or an orthopedic surgeon to perform the procedure. Post-surgery therapy and strengthening may be needed, depending on the tumor location and health of the individual. While shown to be effective, surgical resection has many potential complications, including difficult intraoperative identification of the tumor, local recurrence from incomplete resection, and resection of weight bearing bone that can necessitate prolonged hospital stays and complicate recovery.[11]. Recently, CT guided radiofrequency ...
... Albert N. Van Geel,1,2 Hans M. Hazelbag,3 Rob Slingerland,4 and Margit I. Vermeulen1 ... All types of adamantinoma should be treated by complete en bloc resection. For patients with metastatic spread to the lungs, ... This report describes a patient with a primary long bone adamantinoma. The lesion was initially wrongly diagnosed as fibrous ... the tumour had progressed from an osteofibrous dysplasia-like to a full-blown classic adamantinoma, with metastatic potential ...
"A classic adamantinoma arising from osteofibrous dysplasia-like adamantinoma in the lower leg: a case report and review of the ... Benign osteofibrous dysplasia may be a precursor of adamantinoma or a regressive phase of adamantinoma. Histologically, islands ... Adamantinoma (from the Greek word adamantinos, meaning "very hard") is a rare bone cancer, making up less than 1% of all bone ... "Adamantinoma: Overview - eMedicine". Archived from the original on 25 December 2008. Retrieved 2009-01-04. Fischer B. Uber ein ...
... adamantinoma explanation free. What is adamantinoma? Meaning of adamantinoma medical term. What does adamantinoma mean? ... Looking for online definition of adamantinoma in the Medical Dictionary? ... adamantinoma. /ad·a·man·ti·no·ma/ (ad″ah-man″tĭ-no´mah) ameloblastoma.. adamantinoma, adamantoblastoma. See ameloblastoma. ... Our understanding of the relationship among classic adamantinoma, differentiated adamantinoma (osteofibrous dysplasia-like ...
Adamantinoma is a rare bone cancer ( 0.1-0.5% of all primary bone tumors ). Risk factors in the development of adamantinoma may ... Adamantinoma was first discovered by Fischer in 1913.[1] Classification. Adamantinoma is classified into 2 distinct types: ... There are no ECG findings associated with adamantinoma. X-ray. An x-ray may be helpful in the diagnosis of adamantinoma. ... Adamantinoma may present with bowing deformity of the tibia. There is no medical therapy for adamantinoma. Radiation therapy ...
Adamantinoma of Long Bone (extragnathic adamantinoma): Adamantinoma is a rare primary low-grade malignant tumor of bone that is ... Adamantinoma of Long Bone (extragnathic adamantinoma): Adamantinoma is a rare primary low-grade malignant tumor of bone that is ... Adamantinoma at Orthonet Location: http://www.orthonet.on.ca/adamantinoma/ Adamantinoma - 1o bone tumor with predilection for ... Adamantinoma of the long bone is not related to adamantinoma or ameloblastoma of the mandible and maxilla, which is derived ...
... adamantoma explanation free. What is adamantoma? Meaning of adamantoma medical term. What does adamantoma mean? ... Looking for online definition of adamantoma in the Medical Dictionary? ... adamantoma. adamantoma. /ad·a·man·to·ma/ (ad″ah-man-to´mah) ameloblastoma.. adamantoblastoma, adamantoma. see ameloblastoma. ... Adamantoma , definition of adamantoma by Medical dictionary https://medical-dictionary.thefreedictionary.com/adamantoma ...
Adamantinoma is low grade malignant tumor of fibroblast origin. Also called as primary epidermoid carcinoma of bone, malignan ... Rarely,(11;22) translocations have been reported in case of adamantinoma, and is termed adamantinoma-like ewings sarcoma.11 11 ... Pain may be present due to history of repetitive trauma associated with adamantinoma.7 Adamantinoma is low grade malignant ... Adamantinoma is low grade malignant tumor of fibroblast origin. Also called as primary epidermoid carcinoma of bone, malignant ...
Adamantinoma is a rare tumour of long bones, representing less than 1% of them. Adamantinoma commonly occurs in the tibia. It ... Adamantinoma of the tibia and fibula with pulmonary metastasis: an unusual presentation ... Adamantinoma of the tibia and fibula with pulmonary metastasis: an unusual presentation ...
Adamantinoma-like Ewing sarcoma (ALES) is a rare variant of Ewing sarcoma that is defined by complex epithelial differentiation ... Adamantinoma-like Ewings sarcoma and Ewings-like adamantinoma. The t(11; 22), t(21; 22) status. J Pathol. 2001;195(2):218-21. ... Adamantinoma-Like Ewings family tumor of the sino nasal region: a case report and a brief review of literature. Case Rep ... Adamantinoma-like Ewing family tumor of soft tissue associated with the vagus nerve: a case report and review of the literature ...
Fingerprint Dive into the research topics of Sinonasal adamantinoma-like Ewing sarcoma: A case report. Together they form a ...
Todays topic is - ADAMANTINOMA ! (and no its not what would only happen to Wolverine! Haha see what I did there ?! ) ...
MalaCards based summary : Adamantinoma of Long Bones, also known as long bone adamantinoma, is related to tibial adamantinoma ... MalaCards integrated aliases for Adamantinoma of Long Bones:. Name: Adamantinoma of Long Bones 56 58 43 ... MalaCards organs/tissues related to Adamantinoma of Long Bones:. 40 Bone, Eye, Testes, Colon, Breast, Skin ... Morphologic diversity of long bone adamantinoma. The concept of differentiated (regressing) adamantinoma and its relationship ...
Adamantinoma Adamantinoma is a rare malignant bone tumor most commonly found in the tibia. Contact the Orthopaedic Oncology ...
Adamantinoma and hamartoma tissue array, 40 cases_80 cores \ MC804 for more molecular products just contact us ... Adamantinoma and hamartoma tissue microarray, containing 22 cases of bone adamantinoma, 18 hamartoma of kidney and liver, ... We have also other products like : Adamantinoma and hamartoma tissue array, 40 cases_80 cores. Related products : Adamantinoma ... Index / US Biomax / Adamantinoma and hamartoma tissue array, 40 cases_80 cores / Product Detail : MC804 Adamantinoma and ...
The name adamantinoma was given to this tumor because of its histologic resemblance to the more common adamantinoma ( ... Figure 24.2. Adamantinoma involving the tibia and fibula in a 19-year-old woman. A: Extensive involvement of the cortex of the ... Some cases of adamantinoma have also been reported in short tubular bones, but the diagnoses in these cases have to be ... Adamantinoma of long bones is a peculiar neoplasm that, on the basis of radiographic and pathologic features, arises within the ...
Tumor Library - Cancer Oncology - Welcome to the James O. Johnston Orthopaedic Oncology Tumor Library. This site is intended to offer the oppotunity to cancer research of Orthopaedic Oncology diagnosis slides and imagery from Dr. Johnson s personal library.
Background: Adamantinoma arising in the femur is extremely rare. We report a case of an adamantinoma occurring in the right ... N2 - Background: Adamantinoma arising in the femur is extremely rare. We report a case of an adamantinoma occurring in the ... AB - Background: Adamantinoma arising in the femur is extremely rare. We report a case of an adamantinoma occurring in the ... abstract = "Background: Adamantinoma arising in the femur is extremely rare. We report a case of an adamantinoma occurring in ...
Adamantinoma Adamantinoma is a rare bone cancer that almost always occurs in the bones of the lower leg. Adamantinomas account ...
Adamantinoma-like Ewings sarcoma. Genomic confirmation, phenotypic drift. Julia A. Bridge, Mary E. Fidler, James R. Neff, ... Adamantinoma-like Ewings sarcoma: Genomic confirmation, phenotypic drift. American Journal of Surgical Pathology. 1999 Feb 1; ... Adamantinoma-like Ewings sarcoma : Genomic confirmation, phenotypic drift. / Bridge, Julia A.; Fidler, Mary E.; Neff, James R ... keywords = "Adamantinoma, EWS/FLI1, Ewings sarcoma, Karyotype, RT/PCR",. author = "Bridge, {Julia A.} and Fidler, {Mary E.} ...
1 adamantinoma of jaw 2005:2010[pubdate] *count=100 25 results Searchbox Export PDF RSS Email Delete Email this search result ... Kitsoulis P, Charchanti A, Paraskevas G, Marini A, Karatzias G: Adamantinoma. Acta Orthop Belg; 2007 Aug;73(4):425-31. [ ... Ameloblastoma (adamantinoma) is a benign neoplasm deriving from the enamel organ.. * About 20% of described cases of ... Adamantinoma is one of the rarest low-grade malignant bone tumours, representing less than 1% of them. ...
So-called "Adamantinoma of Long Bone". Zand, Abbas; Chambers, George H.; Street, Dana M. ...
Adamantinoma of Long Bone (extragnathic adamantinoma): Adamantinoma is a rare primary low-grade malignant tumor of bone that is ... Adamantinoma of the long bone is not related to adamantinoma or ameloblastoma of the mandible and maxilla, which is derived ... state that there is an entity known as osteofibrous dyplasia-like adamantinoma (differentiated adamantinoma) that may be a ... Adamantinoma usually presents as an intraosseous, intracortical stage I-A sarcoma.. This low-grade, slowly-growing malignancy ...
Preoperative radiographs show a teenage patient with a tibial adamantinoma (A-B). The decision was made to treat the patient ...
24.89 Adamantinoma of tibia. Lack of cohesiveness of tumor cells in some of the islands results in a pseudovascular appearance ... 24.91 Immunoreactivity for keratin in the tumor cells of adamantinoma of tibia. ...
Adamantinoma. Rhabdoid Tumor. Paraganglioma. Carotid Body Tumor. Choroid Plexus Neoplasms. Pinealoma. Optic Nerve Glioma. ...
Adamantinoma. Endocrine System Diseases. Hypothalamic Diseases. Brain Diseases. Central Nervous System Diseases. Nervous System ...
Tumors can originate in any type of bone cells, and they can be either benign (non-cancerous) or malignant (cancer). Bone cancers can also be:. Primary: These are cancers that originate in the bone.. Metastatic: These are cancers that start in other parts of the body - such as the lung, breast, or prostate - and spread to the bone. Metastatic cancers in the bone are more common than primary bone cancers.. ...
Scintigraphic Findings of Tibial Adamantinoma on a Three-Phase Bone Scan. USUI, KOKI; YAMAMOTO, WAKAKO; SHUKE, NORIYUKI; More ...
This book reflects the experience of the Rizzoli Orthopedic Institute during more than 100 years of treatment of musculoskeletal tumor and tumorlike lesions. It presents a wide range of lesions from a
Adamantinoma Imaging * Benign Skull Tumors * A 13-Year-Old Boy With Recurrent Lower Leg Pain ...
  • Adamantinoma is a low grade, malignant bone tumor. (wikidoc.org)
  • Atlas of Genetics and Cytogenetics in Oncology and Haematology (AGCOH) Adamantinoma of long bones is a low-grade, malignant biphasic tumor, characterized by a variety of morphological patterns, most commonly epithelial cells, surrounded by a relatively bland spindle-cell osteo-fibrous component. (orthopaedicweblinks.com)
  • Adamantinoma - 1o bone tumor with predilection for tibial diaphysis presenting during early adulthood Signs & Symptoms: - painful masses with variable symptom duration ranging from few months to few years Xrays: - well-circumscribed, eccentric, lytic lesions of tibial diaphysis - may be multicystic lesion with surrounding sclerosis - expansion of bone +/- intact cortex but no. (orthopaedicweblinks.com)
  • Adamantinoma is a rare tumor, and its origin remains controversial. (orthopaedicweblinks.com)
  • Adamantinoma is low grade malignant tumor of fibroblast origin. (ukessays.com)
  • The first bone tumor with epithelial characteristic was reported by Maier in 1900, later in 1913 Fischer termed it as adamantinoma. (ukessays.com)
  • 7 Adamantinoma is low grade malignant tumor, and can metastasize to loco-regional nodal areas and to lungs at presentation. (ukessays.com)
  • Adamantinoma-like Ewing family tumor of soft tissue associated with the vagus nerve: a case report and review of the literature. (springer.com)
  • Adamantinoma-Like Ewing's family tumor of the sino nasal region: a case report and a brief review of literature. (springer.com)
  • Adamantinoma is a rare malignant bone tumor most commonly found in the tibia. (massgeneral.org)
  • The name adamantinoma was given to this tumor because of its histologic resemblance to the more common adamantinoma (ameloblastoma) of the jawbones. (musculoskeletalkey.com)
  • The histological similarity of the lung tumor and the femoral tumor led to the diagnosis of adamantinoma arising in her right medial femoral condyle with metastasis to the upper lobe of her right lung. (elsevier.com)
  • Adamantinoma is a rare primary low-grade malignant tumor of bone that is locally aggressive. (wikibooks.org)
  • Approximately 60% of patients with adamantinoma have a history of trauma, including fractures, to the affected bone, but it is unclear whether trauma is involved with formation of the tumor or the formation of the tumor leaves the bone weak and susceptible to injury. (wikibooks.org)
  • report a case of recurrent adamantinoma with metastasis to the lungs that was successfully retreated with surgical resection of the recurrent tumor and metastases. (wikibooks.org)
  • Fig. 24.91 Immunoreactivity for keratin in the tumor cells of adamantinoma of tibia. (slideshare.net)
  • Adamantinoma of the long bones, or extragnathic adamantinoma, is an extremely rare, slow growing, low-grade malignant tumor of epithelial origin, that occurs almost exclusively in the tibia and the fibula. (reininsarcoma.org)
  • Chondroblastoma Epiphyses Giant Cell tumor Epiphyses Adamantinoma Tibia Chordoma Sacrum. (scribd.com)
  • Acanthomatous (also called Oral Adamantinoma) is a locally invasive, sometimes recurrent, tumor of the gums of dogs and sometimes cats. (streetdirectory.com)
  • An Adamantinoma is a rare slow growing type of cancerous bone tumor that occurs most often in boys and young men, most frequently found in the shin bone, and jaw bone. (nicklauschildrens.org)
  • Journal of Clinical and Experimental Orthopaedics considers articles on clinical orthopaedics related issues such as Adamantinoma, Aneurysmal Bone Cysts ,Chondrosarcoma Chordomas Cryosurgery Enchondroma , Fibrous Dysplasia, Giant Cell Tumor of Bone, Malignant Osteoid ,Metastatic Bone Cancer Multilobular Tumour of Bone Orthopaedic Oncology Osteocartilaginous Exostosis Osteochondrodysplasia Osteoma Osteonecrosis Osteosarcoma Primary Bone Tumors Secondary Bone Tumours Tumours of Bone. (imedpub.com)
  • Adamantinoma, malignant biphasic tumor, management. (jbstjournal.com)
  • At second local recurrence, the tumour had progressed from an osteofibrous dysplasia-like to a full-blown classic adamantinoma, with metastatic potential to the lungs 19 years after the initial treatment. (hindawi.com)
  • citation needed] Benign osteofibrous dysplasia may be a precursor of adamantinoma or a regressive phase of adamantinoma. (wikipedia.org)
  • Adamantinoma is classified into 2 distinct types: classic and differentiated (Osteofibrous dysplasia (OFD) - like). (wikidoc.org)
  • Risk factors in the development of adamantinoma may include benign osteofibrous dysplasia . (wikidoc.org)
  • The radiographic features of adamantinoma and osteofibrous dysplasia of the tibia are generally identical. (wikibooks.org)
  • Adamantinoma, fibrous dysplasia and osteofibrous dysplasia (ossifying fibroma) share many radiographic and pathological features, but their interrelationships are unclear. (wikibooks.org)
  • Osteofibrous dysplasia and adamantinoma: correlation of proto-oncogene product and matrix protein expression. (ox.ac.uk)
  • To investigate the relationship between osteofibrous dysplasia (OFD) and adamantinoma, we analyzed the expression of several proto-oncogene products and extracellular matrix proteins by immunohistochemistry and correlated our results with histological and ultrastructural findings. (ox.ac.uk)
  • 2. Kahn LB. Adamantinoma, osteofibrous dysplasia and differentiated adamantinoma. (jbstjournal.com)
  • The concept of differentiated (regressing) adamantinoma and its relationship to osteofibrous dysplasia. (jbstjournal.com)
  • Others have considered congenital rests of epithelium as the source of the tumors, and still others have stated that the so-called adamantinoma of long bones is not epithelial at all but represents an unusual manifestation of sarcoma, either synovial sarcoma or angiosarcoma. (musculoskeletalkey.com)
  • 5 The characteristic features of adamantinoma is slow, gradual development with high chances of local recurrences and also metastases to lungs. (ukessays.com)
  • It is possible that several histogenetically different tumors can produce the features of adamantinoma. (musculoskeletalkey.com)
  • Lung infiltration also showed features of adamantinoma. (bioline.org.br)
  • In 1885, this kind of odontogenic neoplasm was designated as an adamantinoma by Malassez and was finally renamed to the modern name ameloblastoma in 1930 by Ivey and Churchill. (wikipedia.org)
  • Adamantinoma of the long bone is not related to adamantinoma or ameloblastoma of the mandible and maxilla, which is derived from Rathke's pouch. (wikibooks.org)
  • state that there is an entity known as osteofibrous dyplasia-like adamantinoma (differentiated adamantinoma) that may be a precursor to classic adamantinoma. (wikibooks.org)
  • JRC:3170 : Classic adamantinoma (Bone: tibia). (humpath.com)
  • 1990) demonstrated a translocation t(7;13)(q32;q14) in a lung metastasis from an adamantinoma of the tibia in a boy who showed the. (orthopaedicweblinks.com)
  • Sandeep Kanakaraddi, T. M. Ravinath, G. Nagaraj: Adamantinoma Of Tibia With Skeletal Metastasis: An Unusual Presentation. (orthopaedicweblinks.com)
  • The tumour has penetrated into the knee joint by way of direct perforation through the articular surface or via the collateral or cruciate ligaments or as a skip metastasis.The resection entails complete resection of the knee en bloc with the corresponding defect of both the tibia as well as femur. (scielo.org.za)
  • Adamantinoma Tibia Chordoma Sacrum. (scribd.com)
  • Epithelioid sarcoma, chordoma, and adamantinoma show strong positivity corresponding to that of simple epithelia (with antibodies against CK8, CK18 and CK19). (novusbio.com)
  • If left untreated, 15-30% of patients with adamantinoma may metastasize to other parts of the body such as lungs or nearby lymph nodes . (wikidoc.org)
  • The majority of patients with adamantinoma are adolescents and young adults. (musculoskeletalkey.com)
  • Adamantinoma-like Ewing family tumors of the head and neck: a pitfall in the differential diagnosis of basaloid and myoepithelial carcinomas. (springer.com)
  • Ongkeko M, Zeck J, deBrito P. Molecular testing uncovers an adamantinoma-like ewing family of tumors in the thyroid: case report and review of literature. (springer.com)
  • Adamantinoma represents a distinct group of bone tumors showing both mesenchymal and epithelial differentiation most commonly involving the tibial diaphysis. (elsevier.com)
  • FISH of eight additional bone tumors initially classified as spindle cell adamantinoma based on clinicoradiopathologic findings revealed one additional case with SS18 rearrangement. (elsevier.com)
  • Adamantinoma-like Ewing sarcoma (ALES) is a rare variant of Ewing sarcoma that is defined by complex epithelial differentiation, including expression of cytokeratin and p40 and frequent keratin pearl formation. (springer.com)
  • Adamantinoma-like Ewing's sarcoma: genomic confirmation, phenotypic drift. (springer.com)
  • Adamantinoma-like Ewing's sarcoma with EWS-FLI1 fusion gene: a case report. (springer.com)
  • Sinonasal adamantinoma-like Ewing sarcoma: a case report. (springer.com)
  • Adamantinoma-like Ewing sarcoma mimicking basal cell adenocarcinoma of the parotid gland: a case report and review of the literature. (springer.com)
  • Adamantinoma-like Ewing sarcoma of the parotid gland: cytopathologic findings and differential diagnosis. (springer.com)
  • Adamantinoma-Like Ewing sarcoma of the thyroid: a case report and review of the literature. (springer.com)
  • Adamantinoma-like Ewing sarcoma of the salivary glands: a newly recognized mimicker of basaloid salivary carcinomas. (springer.com)
  • Adamantinoma of Long Bones, also known as long bone adamantinoma , is related to tibial adamantinoma and biphasic synovial sarcoma . (malacards.org)
  • Adamantinoma of extragnathic bones, a low-grade malignant neoplasm with epithelial features, is not typically considered in the differential diagnosis of Ewing's sarcoma. (elsevier.com)
  • Adamantinoma usually presents as an intraosseous, intracortical stage I-A sarcoma. (wikibooks.org)
  • However, the relationship between spindle cell adamantinoma and intraosseous synovial sarcoma has not been investigated. (elsevier.com)
  • Histologically, both intraosseous synovial sarcoma and spindle cell adamantinoma demonstrated uniform fusiform nuclei with scant cytoplasm, short fascicles and low mitotic activity. (elsevier.com)
  • The above findings highlight the morphologic and immunophenotypic overlap between spindle cell adamantinoma and intraosseous synovial sarcoma of the tibia. (elsevier.com)
  • Investigation of SS18 status to exclude synovial sarcoma is suggested prior to rendering a diagnosis of spindle cell adamantinoma. (elsevier.com)
  • The lesion on the far left was thought to be an adamantinoma because of the localisation in the anterior tibial cortex. (radiologyassistant.nl)
  • These findings would be in keeping with the hypothesis that OFD represents a precursor lesion of adamantinoma. (ox.ac.uk)
  • Treatment of adamantinoma is wide surgical excision - neither radiation therapy or chemotherapy is effective. (wikibooks.org)
  • The diagnosis of adamantinoma is based on the findings of radiologic studies such as x-ray , CT, and MRI . (wikidoc.org)
  • Adamantinoma was considered, however, the diagnosis was inconclusive due to the unusual localization and her age. (elsevier.com)
  • We report a case of local recurrence of an adamantinoma localised in tibia, along with the presence of two lung metastases, 24 years after diagnosis and surgical therapy of the primary tumour. (bioline.org.br)
  • 1 The near-benign nature of adamantinoma, in terms of biological aggressiveness, is reflected on the prolonged period of vague symptoms before diagnosis and good survival rates even after the diagnosis of local recurrence or metastases. (bioline.org.br)
  • Past history revealed that the patient was operated upon 24 years ago for a pathological fracture of the right tibia and the diagnosis at that time had been adamantinoma. (bioline.org.br)
  • Fine needle aspiration (FNA) biopsy confirmed the diagnosis of adamantinoma of right tibia suggesting local recurrence. (bioline.org.br)
  • The pathological examination of the excised tumour confirmed the diagnosis of adamantinoma set by FNA biopsy ( Figure 3 ). (bioline.org.br)
  • When FD in the tibia is considered, adamantinoma should be in the differential diagnosis. (radiologyassistant.nl)
  • This report describes a patient with a primary long bone adamantinoma. (hindawi.com)
  • Morphologic diversity of long bone adamantinoma. (jbstjournal.com)
  • All types of adamantinoma should be treated by complete en bloc resection. (hindawi.com)
  • An extra-articular resection involves the 'en bloc' resection of the joint with the resection lines being beyond the bounds of the joint. (scielo.org.za)
  • Amputation does not improve survival but may be advisable in cases with local recurrence and in cases with few large, recurrent lesions where en bloc resection is not possible. (jbstjournal.com)
  • 6 In this case study, we have presented a rare histological acanthomatous variant of adamantinoma of the right tibia with metastases to the right inguinal region. (ukessays.com)
  • Differential expression of a number of bone matrix protein in adamantinoma may also be of diagnostic use in distinguishing these 2 lesions immunohistochemically. (ox.ac.uk)
  • Adamantinoma is a rare tumour of long bones, representing less than 1% of them. (bmj.com)
  • 2 The exact origin of adamantinoma is unknown, the classic variant is composed of epithelial cells and osteofibrous components. (ukessays.com)
  • Adamantinoma was first discovered by Fischer in 1913. (wikidoc.org)
  • The current study was prompted by identification of a presumed spindle cell adamantinoma of the tibia with diffuse keratin expression that harbored a SS18 gene region rearrangement. (elsevier.com)
  • The histological examination revealed a multiforming adamantinoma with basaloid, spindle cellular, and tubular characteristics. (bioline.org.br)
  • Adamantinoma of tibia: a case of late local recurrence along with lung metastases. (orthopaedicweblinks.com)
  • An important gene associated with Adamantinoma of Long Bones is EGF (Epidermal Growth Factor), and among its related pathways/superpathways are Neural Stem Cell Differentiation Pathways and Lineage-specific Markers and Lung fibrosis . (malacards.org)
  • Adamantinomas are considered malignant neoplasms requiring en bloc excision that frequently recur locally and can rarely metastasize. (elsevier.com)
  • Conclusion: In this case report, we report the clinical, radiographic, and histological features of an adamantinoma arising in the distal femur with a review of the literature. (elsevier.com)
  • Contact the Orthopaedic Oncology Service at Mass General for more information about treatment for Adamantinoma. (massgeneral.org)
  • Adamantinoma (from the Greek word adamantinos, meaning "very hard") is a rare bone cancer, making up less than 1% of all bone cancers. (wikipedia.org)
  • Adamantinoma of the long bones is a rare, low-grade malignant neoplasm of unknown histogenesis, which affects mainly the tibia of young adults (Keeney et al. (orthopaedicweblinks.com)
  • Background: Adamantinoma arising in the femur is extremely rare. (elsevier.com)
  • Adamantinoma is a rare bone cancer that almost always occurs in the bones of the lower leg. (pennmedicine.org)
  • I joined CanTeen as a patient member after being diagnosed with a rare form of bone cancer called Adamantinoma. (scoop.co.nz)
  • Adamantinoma of long bones: clinical, pathological and ultrastructural features. (orthopaedicweblinks.com)
  • 12 An adamantinoma that is located in the long bones and results in focal epithelial differentiation. (malacards.org)
  • Adamantinoma of long bones is a peculiar neoplasm that, on the basis of radiographic and pathologic features, arises within the osseous substance. (musculoskeletalkey.com)
  • There are 44 examples of adamantinoma of long bones in the Mayo Clinic files ( Fig. 24.1 ). (musculoskeletalkey.com)
  • Some cases of adamantinoma have also been reported in short tubular bones, but the diagnoses in these cases have to be considered suspect. (musculoskeletalkey.com)
  • MRI of adamantinoma of long bones in correlation with histopathology. (jbstjournal.com)
  • Adamantinoma of the long bones: Keratin subclass immunoreactivity pattern with reference to its histogenesis. (jbstjournal.com)
  • 19. Qureshi AA, Shott S, Mallin BA, Gitelis S. Current trends in the management of adamantinoma of long bones. (jbstjournal.com)
  • Expression of growth factors and their receptors in adamantinoma of long bones and the implication for its histogenesis. (jbstjournal.com)
  • MRI findings in adamantinoma are non-specific, but can help demonstrate intraosseous and extrasseous involvement. (wikibooks.org)
  • A S Pieterse, P S Smith, and J McClure Abstract The clinical, pathological and ultrastructural features of two cases of tibial adamantinoma are described. (orthopaedicweblinks.com)
  • Page : 57-8 Surana SS, Mogra NK, Dube MK, Dhruva AK Adamantinoma of tibia is a rarely encountered neoplasm of dispute histogenesis and variable clinical. (orthopaedicweblinks.com)
  • This case report refers to an atypical clinical course of an adamantinoma of the tibia. (bioline.org.br)