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Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin

Spontaneous tumor lysis syndrome (STLS) is a rare oncologic emergency caused by massive cancer cell lysis or necrosis without a precipitating factor. Although tumor lysis syndrome (TLS) is most commonly associated with hematologic malignancies, a small number of cases in solid tumor malignancies hav...

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Detalles Bibliográficos
Autores principales: Kalter, Joshua A, Allen, Jamie, Yang, Yuchen, Willing, Tyler, Evans, Elizabeth
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cureus 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813933/
https://www.ncbi.nlm.nih.gov/pubmed/33489580
http://dx.doi.org/10.7759/cureus.12169
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author Kalter, Joshua A
Allen, Jamie
Yang, Yuchen
Willing, Tyler
Evans, Elizabeth
author_facet Kalter, Joshua A
Allen, Jamie
Yang, Yuchen
Willing, Tyler
Evans, Elizabeth
author_sort Kalter, Joshua A
collection PubMed
description Spontaneous tumor lysis syndrome (STLS) is a rare oncologic emergency caused by massive cancer cell lysis or necrosis without a precipitating factor. Although tumor lysis syndrome (TLS) is most commonly associated with hematologic malignancies, a small number of cases in solid tumor malignancies have been reported. We present a case of spontaneous tumor lysis syndrome in a 77-year-old female with a widely metastatic, poorly differentiated adenocarcinoma of unknown origin. She presented in distributive shock, and laboratory testing at admission revealed acute renal failure, high anion gap metabolic acidosis, hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. Rasburicase and continuous renal replacement therapy were initiated, however, her condition deteriorated. Treatment was withdrawn and she died four days after admission. 
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spelling pubmed-78139332021-01-22 Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin Kalter, Joshua A Allen, Jamie Yang, Yuchen Willing, Tyler Evans, Elizabeth Cureus Emergency Medicine Spontaneous tumor lysis syndrome (STLS) is a rare oncologic emergency caused by massive cancer cell lysis or necrosis without a precipitating factor. Although tumor lysis syndrome (TLS) is most commonly associated with hematologic malignancies, a small number of cases in solid tumor malignancies have been reported. We present a case of spontaneous tumor lysis syndrome in a 77-year-old female with a widely metastatic, poorly differentiated adenocarcinoma of unknown origin. She presented in distributive shock, and laboratory testing at admission revealed acute renal failure, high anion gap metabolic acidosis, hyperuricemia, hyperkalemia, hyperphosphatemia, and hypocalcemia. Rasburicase and continuous renal replacement therapy were initiated, however, her condition deteriorated. Treatment was withdrawn and she died four days after admission.  Cureus 2020-12-19 /pmc/articles/PMC7813933/ /pubmed/33489580 http://dx.doi.org/10.7759/cureus.12169 Text en Copyright © 2020, Kalter 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 Emergency Medicine
Kalter, Joshua A
Allen, Jamie
Yang, Yuchen
Willing, Tyler
Evans, Elizabeth
Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title_full Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title_fullStr Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title_full_unstemmed Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title_short Spontaneous Tumor Lysis Syndrome in an Adenocarcinoma of Unknown Origin
title_sort spontaneous tumor lysis syndrome in an adenocarcinoma of unknown origin
topic Emergency Medicine
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7813933/
https://www.ncbi.nlm.nih.gov/pubmed/33489580
http://dx.doi.org/10.7759/cureus.12169
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