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Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria
BACKGROUND: This case report describes a cystic fibrosis case after 7 years of a presumed diagnosis of celiac disease without confirming laboratory tests and biopsies. Both cystic fibrosis and celiac disease cause malnutrition, malabsorption, and failure to thrive. Also, the occurrence of cystic fib...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088139/ https://www.ncbi.nlm.nih.gov/pubmed/37038158 http://dx.doi.org/10.1186/s12887-023-03982-7 |
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author | Ranjous, Yahia Al Balkhi, Abdulrahman Alahmad, Nazir Asaad, Ali Ali, Ayman |
author_facet | Ranjous, Yahia Al Balkhi, Abdulrahman Alahmad, Nazir Asaad, Ali Ali, Ayman |
author_sort | Ranjous, Yahia |
collection | PubMed |
description | BACKGROUND: This case report describes a cystic fibrosis case after 7 years of a presumed diagnosis of celiac disease without confirming laboratory tests and biopsies. Both cystic fibrosis and celiac disease cause malnutrition, malabsorption, and failure to thrive. Also, the occurrence of cystic fibrosis in celiac disease patients is higher than in the normal population. Therefore, the differentiation between the two diseases might be challenging. This article highlights the reason for the confusion between cystic fibrosis and celiac disease and emphasizes the importance of not skipping the necessary investigations no matter how difficult it is to perform them. CASE PRESENTATION: This report details the case history of a patient presumed to have celiac disease for 7 years without confirming investigations. He developed multiple respiratory infections and weight loss throughout the 7 years but was only diagnosed with cystic fibrosis after hospitalization for gradual abdominal distension and productive cough. Chest CT showed atelectasis in the right upper lobe, tree-in-bud sign on both sides, and right periumbilical mass with several enlargements in the mediastinal nodes. Ascites paracentesis revealed a high SAAG gradient and low-protein fluid. The sweat chloride test resulted in a chloride level of 90 mEq/L, which confirmed the cystic fibrosis diagnosis. Subsequent genetic testing revealed the rare G85E mutation. CONCLUSION: This report highlights the potential for diagnostic confusion between cystic fibrosis and celiac disease. Also, it reminds physicians about the importance of taking a detailed medical history and performing the essential investigations no matter how difficult it is to do them. Finally, it emphasizes the need to verify the patient’s previous medical history in case there is no official documentation of his case. This should be considered particularly in rural areas in low-income countries where the possibility of medical malpractice should not be forgotten. |
format | Online Article Text |
id | pubmed-10088139 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-100881392023-04-12 Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria Ranjous, Yahia Al Balkhi, Abdulrahman Alahmad, Nazir Asaad, Ali Ali, Ayman BMC Pediatr Case Report BACKGROUND: This case report describes a cystic fibrosis case after 7 years of a presumed diagnosis of celiac disease without confirming laboratory tests and biopsies. Both cystic fibrosis and celiac disease cause malnutrition, malabsorption, and failure to thrive. Also, the occurrence of cystic fibrosis in celiac disease patients is higher than in the normal population. Therefore, the differentiation between the two diseases might be challenging. This article highlights the reason for the confusion between cystic fibrosis and celiac disease and emphasizes the importance of not skipping the necessary investigations no matter how difficult it is to perform them. CASE PRESENTATION: This report details the case history of a patient presumed to have celiac disease for 7 years without confirming investigations. He developed multiple respiratory infections and weight loss throughout the 7 years but was only diagnosed with cystic fibrosis after hospitalization for gradual abdominal distension and productive cough. Chest CT showed atelectasis in the right upper lobe, tree-in-bud sign on both sides, and right periumbilical mass with several enlargements in the mediastinal nodes. Ascites paracentesis revealed a high SAAG gradient and low-protein fluid. The sweat chloride test resulted in a chloride level of 90 mEq/L, which confirmed the cystic fibrosis diagnosis. Subsequent genetic testing revealed the rare G85E mutation. CONCLUSION: This report highlights the potential for diagnostic confusion between cystic fibrosis and celiac disease. Also, it reminds physicians about the importance of taking a detailed medical history and performing the essential investigations no matter how difficult it is to do them. Finally, it emphasizes the need to verify the patient’s previous medical history in case there is no official documentation of his case. This should be considered particularly in rural areas in low-income countries where the possibility of medical malpractice should not be forgotten. BioMed Central 2023-04-11 /pmc/articles/PMC10088139/ /pubmed/37038158 http://dx.doi.org/10.1186/s12887-023-03982-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Case Report Ranjous, Yahia Al Balkhi, Abdulrahman Alahmad, Nazir Asaad, Ali Ali, Ayman Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title | Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title_full | Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title_fullStr | Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title_full_unstemmed | Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title_short | Delayed cystic fibrosis diagnosis due to presumed celiac disease-A case report from Syria |
title_sort | delayed cystic fibrosis diagnosis due to presumed celiac disease-a case report from syria |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10088139/ https://www.ncbi.nlm.nih.gov/pubmed/37038158 http://dx.doi.org/10.1186/s12887-023-03982-7 |
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