Adamantinoma

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Adamantinoma
Micrograph of an adamantinoma showing the biphasic histomorphology. H&E stain..
ICD-O: 9310/0
DiseasesDB 31676
MeSH D050398

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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.

Historical Perspective

The condition was first described by Fischer in 1913.[1][2]

Pathophysiology

Histologically, islands of epithelial cells are found in a fibrous stroma.

Treatment

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.

Template:Epithelial neoplasms


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Template:WikiDoc Sources

  1. Fischer B. Uber ein primares Adamantinom der Tibia. 12. Frankfurt: Zeitschr. f. Path.; 1913:422-441.