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Saul Suster

Researcher at Medical College of Wisconsin

Publications -  484
Citations -  19658

Saul Suster is an academic researcher from Medical College of Wisconsin. The author has contributed to research in topics: Carcinoma & Thymic carcinoma. The author has an hindex of 66, co-authored 470 publications receiving 18256 citations. Previous affiliations of Saul Suster include University of Alabama at Birmingham & University of Alabama.

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Primary synovial sarcomas of the mediastinum: a clinicopathologic, immunohistochemical, and ultrastructural study of 15 cases.

TL;DR: Clinical follow-up was available in 5 patients and showed local recurrence with metastases to lung, lymph nodes, and epidural space from 1 to 3 years in 4 cases and liver metastases and death due to tumor after 6 month in 1 case.
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The oncocytic variant of papillary carcinoma of the thyroid: A clinicopathologic study of 15 cases

TL;DR: Oncocytic papillary carcinoma seems to represent a distinctive morphological variant of carcinoma of the thyroid that in the authors' experience does not appear to behave more aggressively than conventional papilla carcinoma.
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CDX2 is a useful marker of intestinal-type differentiation: a tissue microarray-based study of 629 tumors from various sites.

TL;DR: CDX2 is a useful marker for intestinal-type differentiation, is rarely seen in tumors from the other sites evaluated, and may be useful in determining the site of origin for some metastatic tumors, but is not a sensitive marker for poorly differentiated colorectal carcinoma.
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Epithelioid hemangioendothelioma of the anterior mediastinum. Clinicopathologic, immunohistochemical, and ultrastructural analysis of 12 cases.

TL;DR: Despite their often ominous clinical, radiological, and pathological features, epithelioid hemangioendotheliomas arising in the anterior mediastinum appear to behave as low-grade malignant neoplasms that may be adequately controlled in most instances by surgery alone.
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Benign and malignant salivary gland-type mixed tumors of the lung. Clinicopathologic and immunohistochemical study of eight cases.

TL;DR: This data indicates that primary lung tumors showing features of salivary gland‐type neoplasms are extremely rare and the use of chemotherapy to treat these tumors is a viable option.