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Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone

A 74-year-old female was diagnosed with the autoimmune inflammatory disease temporal arteritis and treated with high and low doses of prednisone over a period of 6 years. During that time, she developed cancers of the lung and colon as well as a soft tumor mass on lumbar vertebrate L3. She also expe...

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Autor principal: Piraino, Frank F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: S. Karger AG 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836169/
https://www.ncbi.nlm.nih.gov/pubmed/29515399
http://dx.doi.org/10.1159/000484714
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author Piraino, Frank F.
author_facet Piraino, Frank F.
author_sort Piraino, Frank F.
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description A 74-year-old female was diagnosed with the autoimmune inflammatory disease temporal arteritis and treated with high and low doses of prednisone over a period of 6 years. During that time, she developed cancers of the lung and colon as well as a soft tumor mass on lumbar vertebrate L3. She also experienced a series of debilitating and disabling symptoms while on prednisone treatment. A temporal analysis of the association of prednisone therapy and immune markers to the successive appearance of the malignant tumors strongly suggests that in the absence of a functioning natural immune and surveillance system by treatment with the immune knockout drug prednisone, spontaneous, multiple independent mutations occurred in several sites in the organ systems of this patient. Over a period of time, these developed into malignant cancers, including a lung nodule which became cancerous 256 days later, as well as the cancers of the colon and a soft tumor mass on lumbar vertebrate L3.
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spelling pubmed-58361692018-03-07 Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone Piraino, Frank F. Case Rep Oncol Case Report A 74-year-old female was diagnosed with the autoimmune inflammatory disease temporal arteritis and treated with high and low doses of prednisone over a period of 6 years. During that time, she developed cancers of the lung and colon as well as a soft tumor mass on lumbar vertebrate L3. She also experienced a series of debilitating and disabling symptoms while on prednisone treatment. A temporal analysis of the association of prednisone therapy and immune markers to the successive appearance of the malignant tumors strongly suggests that in the absence of a functioning natural immune and surveillance system by treatment with the immune knockout drug prednisone, spontaneous, multiple independent mutations occurred in several sites in the organ systems of this patient. Over a period of time, these developed into malignant cancers, including a lung nodule which became cancerous 256 days later, as well as the cancers of the colon and a soft tumor mass on lumbar vertebrate L3. S. Karger AG 2017-11-28 /pmc/articles/PMC5836169/ /pubmed/29515399 http://dx.doi.org/10.1159/000484714 Text en Copyright © 2017 by S. Karger AG, Basel http://creativecommons.org/licenses/by-nc/4.0/ This article is licensed under the Creative Commons Attribution-NonCommercial-4.0 International License (CC BY-NC) (http://www.karger.com/Services/OpenAccessLicense). Usage and distribution for commercial purposes requires written permission.
spellingShingle Case Report
Piraino, Frank F.
Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title_full Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title_fullStr Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title_full_unstemmed Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title_short Multiple Tumor Induction after Treatment of Temporal Arteritis with Prednisone
title_sort multiple tumor induction after treatment of temporal arteritis with prednisone
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5836169/
https://www.ncbi.nlm.nih.gov/pubmed/29515399
http://dx.doi.org/10.1159/000484714
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