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Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer

Osteogenesis imperfecta (OI) is a rare, inherited skeletal disorder characterized by abnormalities of type 1 collagen. Malignancy is rarely reported in patients with OI and it was suggested that this disease can protect against cancer. Here, we report a 41-year-old woman with symptoms of achalasia w...

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Autores principales: Mizrak, Dilsa, Alkan, Ali, Erdogdu, Batuhan, Utkan, Gungor
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385628/
https://www.ncbi.nlm.nih.gov/pubmed/25874139
http://dx.doi.org/10.1155/2015/685459
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author Mizrak, Dilsa
Alkan, Ali
Erdogdu, Batuhan
Utkan, Gungor
author_facet Mizrak, Dilsa
Alkan, Ali
Erdogdu, Batuhan
Utkan, Gungor
author_sort Mizrak, Dilsa
collection PubMed
description Osteogenesis imperfecta (OI) is a rare, inherited skeletal disorder characterized by abnormalities of type 1 collagen. Malignancy is rarely reported in patients with OI and it was suggested that this disease can protect against cancer. Here, we report a 41-year-old woman with symptoms of achalasia where repeated treatment of pneumatic dilation and stent replacement was unsuccessful; therefore, surgery was performed. Pathology showed gastric adenocarcinoma unexpectedly. Chemotherapy was given after assessing dihydropyrimidine dehydrogenase (DPD) enzyme activity, which can be deficient in OI patients. This is the first report of gastric cancer mimicking achalasia in a patient with OI.
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spelling pubmed-43856282015-04-13 Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer Mizrak, Dilsa Alkan, Ali Erdogdu, Batuhan Utkan, Gungor Case Rep Gastrointest Med Case Report Osteogenesis imperfecta (OI) is a rare, inherited skeletal disorder characterized by abnormalities of type 1 collagen. Malignancy is rarely reported in patients with OI and it was suggested that this disease can protect against cancer. Here, we report a 41-year-old woman with symptoms of achalasia where repeated treatment of pneumatic dilation and stent replacement was unsuccessful; therefore, surgery was performed. Pathology showed gastric adenocarcinoma unexpectedly. Chemotherapy was given after assessing dihydropyrimidine dehydrogenase (DPD) enzyme activity, which can be deficient in OI patients. This is the first report of gastric cancer mimicking achalasia in a patient with OI. Hindawi Publishing Corporation 2015 2015-03-22 /pmc/articles/PMC4385628/ /pubmed/25874139 http://dx.doi.org/10.1155/2015/685459 Text en Copyright © 2015 Dilsa Mizrak et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Case Report
Mizrak, Dilsa
Alkan, Ali
Erdogdu, Batuhan
Utkan, Gungor
Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title_full Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title_fullStr Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title_full_unstemmed Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title_short Osteogenesis Imperfecta, Pseudoachalasia, and Gastric Cancer
title_sort osteogenesis imperfecta, pseudoachalasia, and gastric cancer
topic Case Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4385628/
https://www.ncbi.nlm.nih.gov/pubmed/25874139
http://dx.doi.org/10.1155/2015/685459
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