Adamantinoma: Difference between revisions
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{{Infobox Disease | |||
| Name = Adamantinoma | |||
| Image = Adamantinoma - intermed mag.jpg | |||
| Caption = [[Micrograph]] of an adamantinoma showing the biphasic histomorphology. [[H&E stain]].. | |||
| DiseasesDB = 31676 | |||
| ICD10 = | |||
| ICD9 = | |||
| ICDO = 9310/0 | |||
| OMIM = | |||
| MedlinePlus = | |||
| eMedicineSubj = radio | |||
| eMedicineTopic = 11 | |||
| MeshID = D050398 | |||
}} | |||
{{SI}} | {{SI}} | ||
{{CMG}} | |||
==Overview== | ==Overview== | ||
Revision as of 13:33, 10 September 2012
| Adamantinoma | |
| Micrograph of an adamantinoma showing the biphasic histomorphology. H&E stain.. | |
| ICD-O: | 9310/0 |
| DiseasesDB | 31676 |
| eMedicine | radio/11 |
| MeSH | D050398 |
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WikiDoc Resources for Adamantinoma |
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Articles |
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Most recent articles on Adamantinoma Most cited articles on Adamantinoma |
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Media |
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Powerpoint slides on Adamantinoma |
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Evidence Based Medicine |
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Clinical Trials |
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Ongoing Trials on Adamantinoma at Clinical Trials.gov Clinical Trials on Adamantinoma at Google
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Guidelines / Policies / Govt |
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US National Guidelines Clearinghouse on Adamantinoma
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Books |
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News |
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Commentary |
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Definitions |
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Patient Resources / Community |
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Patient resources on Adamantinoma Discussion groups on Adamantinoma Patient Handouts on Adamantinoma Directions to Hospitals Treating Adamantinoma Risk calculators and risk factors for Adamantinoma
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Healthcare Provider Resources |
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Causes & Risk Factors for Adamantinoma |
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Continuing Medical Education (CME) |
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International |
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Business |
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Experimental / Informatics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
Overview
Adamantinoma is a rare bone cancer, making up less than 1% of all bone cancers. It predominantly arises in bone in a subcutaneous location (85% are in the tibia). Most commonly, patients are in their second or third decade, but it can occur over a wide age range.
Histologically, islands of epithelial cells are found in a fibrous stroma.
Treatment consists of wide resection or amputation. Metastases are rare at presentation but may occur in up to 30% of patients during the disease course. Prognosis is excellent, with overall survival of 85% at 10 years, but is lower when wide surgical margins cannot be obtained.
References
- Campbell's Operative Orthopedics (10th edition ed.). 2003.