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Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency

Urea cycle disorders (UCDs) are an unusual genetic condition that may lead to hyperammonemia in catabolic situations such as surgery, infections or chemotherapy administration. Without specific treatment, it causes life-threatening encephalopathy. We present the case of a young woman, heterozygous c...

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Autores principales: Palka-Kotlowska, Magda, Cabezón-Gutiérrez, Luis, Custodio-Cabello, Sara, Quijada-Fraile, PIlar, Chumillas-Calzada, Silvia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317123/
https://www.ncbi.nlm.nih.gov/pubmed/32601573
http://dx.doi.org/10.7759/cureus.8301
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author Palka-Kotlowska, Magda
Cabezón-Gutiérrez, Luis
Custodio-Cabello, Sara
Quijada-Fraile, PIlar
Chumillas-Calzada, Silvia
author_facet Palka-Kotlowska, Magda
Cabezón-Gutiérrez, Luis
Custodio-Cabello, Sara
Quijada-Fraile, PIlar
Chumillas-Calzada, Silvia
author_sort Palka-Kotlowska, Magda
collection PubMed
description Urea cycle disorders (UCDs) are an unusual genetic condition that may lead to hyperammonemia in catabolic situations such as surgery, infections or chemotherapy administration. Without specific treatment, it causes life-threatening encephalopathy. We present the case of a young woman, heterozygous carrier of ornithine transcarbamylase deficiency (OTCD) with breast cancer, who was treated with surgery, chemotherapy, radiotherapy and hormone therapy while following a protocol to minimize the risk of metabolic decompensation due to her condition.
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spelling pubmed-73171232020-06-28 Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency Palka-Kotlowska, Magda Cabezón-Gutiérrez, Luis Custodio-Cabello, Sara Quijada-Fraile, PIlar Chumillas-Calzada, Silvia Cureus Internal Medicine Urea cycle disorders (UCDs) are an unusual genetic condition that may lead to hyperammonemia in catabolic situations such as surgery, infections or chemotherapy administration. Without specific treatment, it causes life-threatening encephalopathy. We present the case of a young woman, heterozygous carrier of ornithine transcarbamylase deficiency (OTCD) with breast cancer, who was treated with surgery, chemotherapy, radiotherapy and hormone therapy while following a protocol to minimize the risk of metabolic decompensation due to her condition. Cureus 2020-05-26 /pmc/articles/PMC7317123/ /pubmed/32601573 http://dx.doi.org/10.7759/cureus.8301 Text en Copyright © 2020, Palka-Kotlowska et al. http://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Internal Medicine
Palka-Kotlowska, Magda
Cabezón-Gutiérrez, Luis
Custodio-Cabello, Sara
Quijada-Fraile, PIlar
Chumillas-Calzada, Silvia
Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title_full Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title_fullStr Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title_full_unstemmed Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title_short Chemotherapy in a Breast Cancer Patient Heterozygous Carrier of Ornithine Transcarbamylase Deficiency
title_sort chemotherapy in a breast cancer patient heterozygous carrier of ornithine transcarbamylase deficiency
topic Internal Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7317123/
https://www.ncbi.nlm.nih.gov/pubmed/32601573
http://dx.doi.org/10.7759/cureus.8301
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