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4. Bladder Cancer

Author

PANTUCK, ALLAN J., primary, LIEBERMAN, RON, additional, KAWAOKA, KELLY, additional, SHVARTS, OLEG, additional, and LAMM, DONALD, additional

Published
2006
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5. Contributing Authors

Author

Aktas, Huseyin, primary, Albanes, Demetrius, additional, Augenlicht, Leonard, additional, Bandera, Elisa V., additional, Barnes, Stephen, additional, Barrett, J. Carl, additional, Bernstein, Leslie, additional, Bheemreddy, Radha M., additional, Black, Homer S., additional, Blackburn, George L., additional, Bonavida, Benjamin, additional, Boros, Laszlo G., additional, Bowerman, Susan, additional, Callahan, Eve, additional, Carpenter, Catherine L., additional, Cella, David, additional, Champaneria, Manish C., additional, Chorev, Michael, additional, Christman, Judith, additional, Cohen, Barbara E., additional, Cohen, Pinchas, additional, D'Alessandro, Tracy, additional, Davis, Paul, additional, Vos, Sven de, additional, Dong, Yan, additional, Dwyer, Johanna, additional, Elashoff, Robert M., additional, El-Bayoumy, Karam, additional, Elson, Charles E., additional, Forman, Michele R., additional, Gao, Allen C., additional, Genkinger, Jeanine, additional, Giarelli, Ellen, additional, Giovannucci, Edward, additional, Go, Vay Liang W., additional, Greenwald, Peter, additional, Guilmeau, Sandra, additional, Halperin, J.A., additional, Hansen, Jason M., additional, Harris, Diane M., additional, Heber, David, additional, Heerdt, Barbara, additional, Hoffmann, Dietrich, additional, Hoque, Ashraful, additional, Hursting, Stephen D., additional, Ip, Clement, additional, Jacobs, Elizabeth T., additional, Jacobs, Linda A., additional, Jeffery, Elizabeth H., additional, Jensen, Gordon L., additional, Jones, Dean P., additional, Kawaoka, Kelly, additional, Khaodhiar, Lalita, additional, Kim, Helen, additional, Klampfer, Lidija, additional, Klurfeld, David M., additional, Koeffler, H. Phillip, additional, Kushi, Lawrence H., additional, Lambert, Joshua D., additional, Lamm, Donald, additional, Landau, Janelle M., additional, Lee, Wai-Nang Paul, additional, Lieberman, Ron, additional, Lippman, Scott, additional, Mahabir, Somdat, additional, Maier, Sandra, additional, Mariadason, John, additional, Marshall, James, additional, Martínez, María Elena, additional, McCullough, Marjorie, additional, McTiernan, Anne, additional, Milner, John, additional, Mo, Huanbiao, additional, Muscat, Joshua E., additional, Nunez, Nomeli P., additional, Ohning, Gordon, additional, Packer, Lester, additional, Pantuck, Allan J., additional, Park, Young-Mee, additional, Parnes, Howard, additional, Perkins, Susan N., additional, Picciano, Mary Frances, additional, Prasain, Jeevan, additional, Reliene, Ramune, additional, Rogers, Connie J., additional, Schiestl, Robert H., additional, Seeram, Navindra P., additional, Shvarts, Oleg, additional, Silver, Heidi J., additional, Smartt, Helena, additional, Smith-Warner, Stephanie A., additional, Taylor, Philip, additional, Tchekmedyian, N. Simon, additional, Thomas, Paul R., additional, Treyzon, Leo, additional, Velcich, Anna, additional, Wang, Chao-Cheng, additional, Welsh, JoEllen, additional, Wu, Yue, additional, Yang, Chung S., additional, Yang, Wancai, additional, You, Nai-chieh Yuko, additional, Zhang, Haitao, additional, Zhang, Huang-Ge, additional, Zhang, Zuo-Feng, additional, and Zhou, Jin-Rong, additional

Published
2006
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24. Carcinoid Tumor of the Kidney: Case Report and Review of the Literature

Author

Shurtleff, Benjamin T, Shvarts, Oleg, and Rajfer, Jacob

Subjects
Case Review
Abstract

Carcinoid tumors are low-grade malignant tumors that arise from neuroendocrine cells. Primary renal carcinoid tumors are extremely uncommon. They seem to be more indolent than renal cell carcinomas, although metastases to regional lymph nodes, liver, and bone have been described. The presence of metastases seems to indicate a more malignant course; however, even with metastases a patient might live for 3 or 4 years. Renal carcinoid tumors should be managed by radical or partial nephrectomy, and good outcomes have been obtained for organ-confined disease after radical excision. Conventional methods of imaging are inadequate for detecting smaller carcinoids, so somatostatin receptor scintigraphy should complement computed tomography and magnetic resonance imaging when searching for occult or metastatic disease. Close follow-up after surgery is necessary.

Published
2005

25. Primary Leiomyosarcoma of the Inferior Vena Cava Presenting as a Renal Mass

Author

Shvarts, Oleg, Han, Ken-Ryu, Lam, John S, and Belldegrun, Arie S

Subjects
cardiovascular system, Case Review
Abstract

Leiomyosarcoma of the inferior vena cava (IVC) is an extremely rare entity. We present the case of a 62-year-old woman who was found to have a large right upper quadrant mass upon examination by her primary care physician in evaluation for diffuse abdominal pain accompanied by anorexia and weight loss. A computed tomographic scan and magnetic resonance imaging demonstrated a 13-cm retroperitoneal lesion that appeared to stem from the right kidney and yielded a tumor thrombus up to the level of the hepatic venous confluence. The patient underwent a right radical nephrectomy and IVC thrombectomy for treatment of a presumed renal cell carcinoma. Instead, pathology revealed the tumor to be a leiomyosarcoma of the IVC. We document this unusual presentation of an extremely rare tumor entity.

Published
2004

34. 1653: Safety and Efficacy of Partial Nephrectomy for all T1 Tumors Based on an International Multicenter Experience

Author

Patard, Jean-Jacques, primary, Shvarts, Oleg, additional, Pantuck, Allan J., additional, Ficarra, Vincenzo, additional, Kim, Hyung L., additional, Cindolo, Luca, additional, Han, Ken, additional, De La Taille, Alexandre, additional, Tostain, Jacques, additional, Artibani, Walter, additional, Abbou, ClementClaude, additional, Lobel, Bernard, additional, Chopin, Dominique, additional, Guille, Franfois, additional, Figlin, Robert A., additional, Mulders, Peter, additional, and Belldegrun, Arie S., additional

Published
2004
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36. Number of metastatic sites rather than location dictates overall survival of patients with node-negative metastatic renal cell carcinoma

Author

Han, Ken-Ryu, primary, Pantuck, Allan J, additional, Bui, Matthew H.T, additional, Shvarts, Oleg, additional, Freitas, Danielo G, additional, Zisman, Amnon, additional, Leibovich, Bradley C, additional, Dorey, Frederick J, additional, Gitlitz, Barbara J, additional, Figlin, Robert A, additional, and Belldegrun, Arie S, additional

Published
2003
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38. RENAL CELL CARCINOMA

Author

TSUI, KE-HUNG, primary, SHVARTS, OLEG, additional, SMITH, ROBERT B., additional, FIGLIN, ROBERT, additional, KERNION, JEAN B. de, additional, and BELLDEGRUN, ARIE, additional

Published
2000
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41. Expanding the Indications for Surgery and Adjuvant Interleukin-2-Based Immunotherapy in Patients with Advanced Renal Cell Carcinoma.

Author

Belldegrun, Arie, Shvarts, Oleg, and Figlin, Robert A.

Abstract

Investigates the role of surgery and adjuvant interleukin (IL)-2-based immunotherapy in the treatment of patients with advanced metastatic renal cell carcinoma. Percentage of patients' survival rates; Safety in aggressive surgery; Effectiveness of surgery with IL-2 immunotherapy regimen.

Published
2000

43. Carcinoid tumor of the kidney: case report and review of the literature.

Author

Shurtleff BT, Shvarts O, and Rajfer J

Abstract

Carcinoid tumors are low-grade malignant tumors that arise from neuroendocrine cells. Primary renal carcinoid tumors are extremely uncommon. They seem to be more indolent than renal cell carcinomas, although metastases to regional lymph nodes, liver, and bone have been described. The presence of metastases seems to indicate a more malignant course; however, even with metastases a patient might live for 3 or 4 years. Renal carcinoid tumors should be managed by radical or partial nephrectomy, and good outcomes have been obtained for organ-confined disease after radical excision. Conventional methods of imaging are inadequate for detecting smaller carcinoids, so somatostatin receptor scintigraphy should complement computed tomography and magnetic resonance imaging when searching for occult or metastatic disease. Close follow-up after surgery is necessary.

Published
2005

44. Primary leiomyosarcoma of the inferior vena cava presenting as a renal mass.

Author

Shvarts O, Han KR, Lam JS, and Belldegrun AS

Abstract

Leiomyosarcoma of the inferior vena cava (IVC) is an extremely rare entity. We present the case of a 62-year-old woman who was found to have a large right upper quadrant mass upon examination by her primary care physician in evaluation for diffuse abdominal pain accompanied by anorexia and weight loss. A computed tomographic scan and magnetic resonance imaging demonstrated a 13-cm retroperitoneal lesion that appeared to stem from the right kidney and yielded a tumor thrombus up to the level of the hepatic venous confluence. The patient underwent a right radical nephrectomy and IVC thrombectomy for treatment of a presumed renal cell carcinoma. Instead, pathology revealed the tumor to be a leiomyosarcoma of the IVC. We document this unusual presentation of an extremely rare tumor entity.

Published
2004

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