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Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease

Patient: Male, 76 Final Diagnosis: Celiac crisis Symptoms: Abdominal pain • bleeding • diarrhea • weakness • weight loss Medication: — Clinical Procedure: Esophagogastroduodenoscopy • Colonoscopy Specialty: Gastroenterology and Hepatology OBJECTIVE: Rare disease BACKGROUND: Celiac crisis is an uncom...

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Autores principales: Gonzalez, Juan J., Elgamal, Mohamed, Mishra, Shikha, Adekolujo, Orimisan S.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410609/
https://www.ncbi.nlm.nih.gov/pubmed/30833539
http://dx.doi.org/10.12659/AJCR.913731
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author Gonzalez, Juan J.
Elgamal, Mohamed
Mishra, Shikha
Adekolujo, Orimisan S.
author_facet Gonzalez, Juan J.
Elgamal, Mohamed
Mishra, Shikha
Adekolujo, Orimisan S.
author_sort Gonzalez, Juan J.
collection PubMed
description Patient: Male, 76 Final Diagnosis: Celiac crisis Symptoms: Abdominal pain • bleeding • diarrhea • weakness • weight loss Medication: — Clinical Procedure: Esophagogastroduodenoscopy • Colonoscopy Specialty: Gastroenterology and Hepatology OBJECTIVE: Rare disease BACKGROUND: Celiac crisis is an uncommon but critical complication of celiac disease (CD) manifesting with copious diarrhea, dehydration, and severe metabolic imbalances. Celiac crisis occurring in individuals who have been formerly diagnosed with CD and displaying severe coagulopathy is tremendously rare. CASE REPORT: We report a case of a 76-year-old male, previously diagnosed with CD and non-compliant with gluten free diet, who presented with severe coagulopathy manifesting as gastrointestinal bleeding in addition to other features of celiac crisis, including severe diarrhea, dehydration, metabolic acidosis, electrolyte disturbances, and renal dysfunction. Esophagogastroduodenoscopy revealed flattened mucosa and mucosal nodularity in the duodenum. Duodenal biopsies exhibited active chronic inflammation with intraepithelial lymphocytosis and subtotal villous blunting. The patient was diagnosed with celiac crisis and treatment with vitamin K, parenteral nutrition, and steroids was commenced. After initial clinical improvement, a gluten-free diet was implemented with complete resolution of symptoms. CONCLUSIONS: Though celiac crisis typically presents in patients with undiagnosed CD, it should be considered in patients who have been previously diagnosed CD but who are non-compliant with gluten free diet. Severe coagulopathy, though extremely rare, can be a feature of celiac crisis and should be consider when encountered in a patient with history of steatorrhea and gastrointestinal bleeding.
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spelling pubmed-64106092019-04-08 Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease Gonzalez, Juan J. Elgamal, Mohamed Mishra, Shikha Adekolujo, Orimisan S. Am J Case Rep Articles Patient: Male, 76 Final Diagnosis: Celiac crisis Symptoms: Abdominal pain • bleeding • diarrhea • weakness • weight loss Medication: — Clinical Procedure: Esophagogastroduodenoscopy • Colonoscopy Specialty: Gastroenterology and Hepatology OBJECTIVE: Rare disease BACKGROUND: Celiac crisis is an uncommon but critical complication of celiac disease (CD) manifesting with copious diarrhea, dehydration, and severe metabolic imbalances. Celiac crisis occurring in individuals who have been formerly diagnosed with CD and displaying severe coagulopathy is tremendously rare. CASE REPORT: We report a case of a 76-year-old male, previously diagnosed with CD and non-compliant with gluten free diet, who presented with severe coagulopathy manifesting as gastrointestinal bleeding in addition to other features of celiac crisis, including severe diarrhea, dehydration, metabolic acidosis, electrolyte disturbances, and renal dysfunction. Esophagogastroduodenoscopy revealed flattened mucosa and mucosal nodularity in the duodenum. Duodenal biopsies exhibited active chronic inflammation with intraepithelial lymphocytosis and subtotal villous blunting. The patient was diagnosed with celiac crisis and treatment with vitamin K, parenteral nutrition, and steroids was commenced. After initial clinical improvement, a gluten-free diet was implemented with complete resolution of symptoms. CONCLUSIONS: Though celiac crisis typically presents in patients with undiagnosed CD, it should be considered in patients who have been previously diagnosed CD but who are non-compliant with gluten free diet. Severe coagulopathy, though extremely rare, can be a feature of celiac crisis and should be consider when encountered in a patient with history of steatorrhea and gastrointestinal bleeding. International Scientific Literature, Inc. 2019-03-05 /pmc/articles/PMC6410609/ /pubmed/30833539 http://dx.doi.org/10.12659/AJCR.913731 Text en © Am J Case Rep, 2019 This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Gonzalez, Juan J.
Elgamal, Mohamed
Mishra, Shikha
Adekolujo, Orimisan S.
Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title_full Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title_fullStr Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title_full_unstemmed Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title_short Severe Coagulopathy as a Rare Feature of Celiac Crisis in a Patient Previously Diagnosed with Celiac Disease
title_sort severe coagulopathy as a rare feature of celiac crisis in a patient previously diagnosed with celiac disease
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6410609/
https://www.ncbi.nlm.nih.gov/pubmed/30833539
http://dx.doi.org/10.12659/AJCR.913731
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