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Congenital Renal Disorders and Kidney Tumors

Autosomal Dominant Polycystic Kidney Disease and Renal Cell Carcinoma

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Contemporary Nephrology

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Abstract

This chapter reviews the literature until May 1986. The first part covers the anatomic and functional correlates of autosomal dominant polycystic kidney disease (ADPKD) and aspects of renal cell carcinoma that will be of interest to nephrologists. Several other tumors that produce symptomatology that is likely to result in nephrologic consultation, such as those seen with acquired cystic disease of dialysis and hemangiopericytoma, are also discussed.

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Authors and Affiliations

  1. Medical Service, Veterans Administration Center, and Departments of Medicine and Physiology, University of Puerto Rico School of Medicine, San Juan, Puerto Rico, 00936

    Manuel Martínez-Maldonado

  2. Renal Section, Veterans Administration Center, and Department of Medicine, University of Puerto Rico School of Medicine, San Juan, Puerto Rico, 00936

    Julio E. Benabe

  3. Hematology Section, Veterans Administration Center, and Department of Medicine, University of Puerto Rico School of Medicine, San Juan, Puerto Rico, 00936

    Luis Báez-Díaz

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  1. Manuel Martínez-Maldonado
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  2. Julio E. Benabe
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  3. Luis Báez-Díaz
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Editors and Affiliations

  1. Washington University School of Medicine, St. Louis, Missouri, USA

    Saulo Klahr M.D.

  2. University of Southern California School of Medicine, Los Angeles, California, USA

    Shaul G. Massry M.D.

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© 1987 Plenum Publishing Corporation

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Martínez-Maldonado, M., Benabe, J.E., Báez-Díaz, L. (1987). Congenital Renal Disorders and Kidney Tumors. In: Klahr, S., Massry, S.G. (eds) Contemporary Nephrology. Springer, Boston, MA. https://doi.org/10.1007/978-1-4613-1859-0_11

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