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Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease
Waldmann's disease, or primary intestinal lymphangiectasia, is an unusual cause of protein‐losing enteropathy primarily characterized by lymphopenia, hypoalbuminemia, and hypogammaglobulinemia. However, variable clinical presentations result dilemmas in diagnosis and effective management. We pr...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9211774/ https://www.ncbi.nlm.nih.gov/pubmed/35769238 http://dx.doi.org/10.1002/ccr3.5992 |
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author | Prajapati, Sarita Bohara, Sujan Mainali, Gaurab Karki, Samikshya Thapa, Sharan Aryal, Nirjala |
author_facet | Prajapati, Sarita Bohara, Sujan Mainali, Gaurab Karki, Samikshya Thapa, Sharan Aryal, Nirjala |
author_sort | Prajapati, Sarita |
collection | PubMed |
description | Waldmann's disease, or primary intestinal lymphangiectasia, is an unusual cause of protein‐losing enteropathy primarily characterized by lymphopenia, hypoalbuminemia, and hypogammaglobulinemia. However, variable clinical presentations result dilemmas in diagnosis and effective management. We present a toddler diagnosed with Waldmann's disease managed with a high‐protein diet and medium‐chain triglyceride supplementation. |
format | Online Article Text |
id | pubmed-9211774 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-92117742022-06-28 Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease Prajapati, Sarita Bohara, Sujan Mainali, Gaurab Karki, Samikshya Thapa, Sharan Aryal, Nirjala Clin Case Rep Case Reports Waldmann's disease, or primary intestinal lymphangiectasia, is an unusual cause of protein‐losing enteropathy primarily characterized by lymphopenia, hypoalbuminemia, and hypogammaglobulinemia. However, variable clinical presentations result dilemmas in diagnosis and effective management. We present a toddler diagnosed with Waldmann's disease managed with a high‐protein diet and medium‐chain triglyceride supplementation. John Wiley and Sons Inc. 2022-06-21 /pmc/articles/PMC9211774/ /pubmed/35769238 http://dx.doi.org/10.1002/ccr3.5992 Text en © 2022 The Authors. Clinical Case Reports published by John Wiley & Sons Ltd. https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Case Reports Prajapati, Sarita Bohara, Sujan Mainali, Gaurab Karki, Samikshya Thapa, Sharan Aryal, Nirjala Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title | Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title_full | Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title_fullStr | Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title_full_unstemmed | Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title_short | Diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: Waldmann's disease |
title_sort | diagnostic dilemma in diagnosing rare cause of protein losing enteropathy: waldmann's disease |
topic | Case Reports |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9211774/ https://www.ncbi.nlm.nih.gov/pubmed/35769238 http://dx.doi.org/10.1002/ccr3.5992 |
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