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Recurrent malignant chondroid syringoma of the foot: a case report and review of the literature.

Authors :
Barnett MD
Wallack MK
Zuretti A
Mesia L
Emery RS
Berson AM
Source :
American journal of clinical oncology [Am J Clin Oncol] 2000 Jun; Vol. 23 (3), pp. 227-32.
Publication Year :
2000

Abstract

Malignant chondroid syringoma, or mixed tumor of the skin, salivary gland type, is an uncommon neoplasm believed to originate in sweat glands. This neoplasm occurs mostly in women and is typically seen in the extremities and torso. A case of recurrent malignant chondroid syringoma of the right foot in a man aged 34 years is described with a review of pertinent literature. The surgically excised neoplasm was evaluated by routine histology, immunohistochemistry, and transmission electron microscopy. The malignant chondroid syringoma showed microscopic dermal satellite tumor nodules. Immunohistochemical staining was positive for keratin and S100 and negative for actin and p53. Ki-67 showed <10% positive staining. Ultrastructurally, the neoplasm was composed of epithelial cells with tonofilaments, cell junctions, and electron-dense amorphous keratin-like substance in the intercellular spaces. No evidence of myoepithelial differentiation was noted. Given the tumoral size, acral location, and histologic findings, the neoplasm was classified as a malignant chondroid syringoma. After reviewing the literature, it became apparent that wide surgical excision, adjuvant radiation therapy as well as patient education are critical in facilitating long-term survival.

Details

Language :
English
ISSN :
0277-3732
Volume :
23
Issue :
3
Database :
MEDLINE
Journal :
American journal of clinical oncology
Publication Type :
Academic Journal
Accession number :
10857882
Full Text :
https://doi.org/10.1097/00000421-200006000-00003