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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...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cureus
2020
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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. |
format | Online Article Text |
id | pubmed-7317123 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Cureus |
record_format | MEDLINE/PubMed |
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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