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  Vol. 122 No. 1, January 2004 TABLE OF CONTENTS
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Orbital Metastasis and Intraocular Invasion of Malignant Mixed Tumor (Carcinosarcoma) of the Parotid Gland in a Child

Arch Ophthalmol. 2004;122:114-118.

Since this article does not have an abstract, we have provided the first 150 words of the full text and any section headings.

Malignant mixed tumor of the salivary glands is a rare neoplasm, and the majority of these tumors arise from the parotid gland.1 Histopathologically, 3 distinct variants of malignant mixed tumors are recognized, the most common being carcinoma arising from a preexisting pleomorphic adenoma.1-2 The second type is the metastasizing mixed tumor, which has benign-appearing epithelial and stromal components.1-2 The true malignant mixed tumor or carcinosarcoma, an exceptionally rare tumor, is the third subtype and is composed of malignant epithelial and malignant mesenchymal elements.2-3

Less than 5% of all salivary gland neoplasms are seen in patients younger than 16 years and 13% of these tumors are solid, of which only 23% are malignant.4 The most common malignant salivary gland tumor in children is mucoepidermoid carcinoma, followed by rhabdomyosarcoma and acinic cell carcinoma.4 We herein describe a highly unusual patient with a carcinosarcoma of the parotid gland that metastasized to ipsilateral orbit . . . [Full Text of this Article]

Report of a Case


Comment
Hayyam Kiratli, MD; Hülya Gökmen Soysal, MD; Süleyman Demir, MD
Ankara, Turkey

Corresponding author: Hayyam Kiratli, MD, Ophthalmology, Hacettepe Hastanesi Goz ABD, Syhhiye 06100, Ankara, Turkey (e-mail: hkiratli@hacettepe.edu.tr).







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