Enfermedad poliquística hepatorrenal complicada con suboclusión intestinal: Reporte de un caso.

Hepatorenal polychistic disease complicated with intestinal suboclusion: A case report.

Authors

DOI:

https://doi.org/10.17268/rmt.2022.v17i3.4218

Keywords:

polycystic liver-renal disease, intestinal subocclusion, cysts, liver, kidney

Abstract

Autosomal Dominant Polycystic Kidney Disease, known by its acronym ADPKD (Autosomal Dominant Polycystic kidney disease), is a condition of genetic origin characterized by two types of mutations in the PKD1 and PKD2 genes that code for polycystins (PC) 1 and 2, respectively. It is associated with extrarenal manifestations, both cystic and non-cystic; the liver is the most affected organ within the cystic manifestations; as well as cerebral vascular alterations, in non-cystic ones. We report a 44-year-old woman with polycystic hepato-renal disease (PLKD) complicated by intestinal subocclusion.

Author Biography

  • Renzzo Amaro Mozo Marquina, , Universidad Nacional de Trujillo, La Libertad, Perú. Estudiante de Medicina.,

    Estudiante de pre-grado de medicina de la Universidad Nacional de Trujillo.

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Published

2022-10-31

Issue

Vol. 17 No. 3 (2022): REVISTA MÉDICA DE TRUJILLO

Section

REPORTE DE CASO

License

Copyright (c) 2022 Revista Médica de Trujillo

Creative Commons License

This work is licensed under a Creative Commons Attribution-NonCommercial 4.0 International License.

How to Cite

1.
Enfermedad poliquística hepatorrenal complicada con suboclusión intestinal: Reporte de un caso.: Hepatorenal polychistic disease complicated with intestinal suboclusion: A case report. Rev Med Trujillo [Internet]. 2022 Oct. 31 [cited 2026 Jul. 18];17(3):121-4. Available from: https://revistas.unitru.edu.pe/index.php/RMT/article/view/4218