Omar Saab, Marwah Algodi, Hasan Al-Obaidi, Alhareth Al-Sagban, Sebouh Setrakian, Alberto Rubio-Tapia
{"title":"一种极为罕见的蛋白质丢失性肠病的病因:Waldenström巨球蛋白血症。","authors":"Omar Saab, Marwah Algodi, Hasan Al-Obaidi, Alhareth Al-Sagban, Sebouh Setrakian, Alberto Rubio-Tapia","doi":"10.14309/crj.0000000000001800","DOIUrl":null,"url":null,"abstract":"<p><p>Protein-losing enteropathy (PLE) results in the abnormal loss of proteins through the gastrointestinal tract, leading to malabsorption and hypoalbuminemia. A rare etiology of PLE is Waldenström macroglobulinemia (WM), a hematological malignancy characterized by immunoglobulin M (IgM) monoclonal gammopathy. We present a case of a 66-year-old man with a history of small bowel bacterial overgrowth and lactose intolerance, admitted for worsening gastrointestinal symptoms, including abdominal discomfort, bloating, and watery diarrhea. He had experienced significant weight loss and anasarca over 6 months. Laboratory tests indicated hypoproteinemia, hypoalbuminemia, and elevated IgM levels, accompanied by abnormal stool studies. Imaging showed no significant findings, while endoscopic evaluation revealed lymphangiectasia-like changes in the small bowel. Biopsy results demonstrated proteinaceous material in dilated villi and IgM deposition. The diagnosis of WM was confirmed by bone marrow biopsy. Thus, WM should be considered when evaluating unexplained PLE, particularly with associated gastrointestinal symptoms and elevated IgM levels.</p>","PeriodicalId":7394,"journal":{"name":"ACG Case Reports Journal","volume":"12 8","pages":"e01800"},"PeriodicalIF":0.5000,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12321444/pdf/","citationCount":"0","resultStr":"{\"title\":\"An Extremely Rare Cause of Protein-Losing Enteropathy: Waldenström Macroglobulinemia.\",\"authors\":\"Omar Saab, Marwah Algodi, Hasan Al-Obaidi, Alhareth Al-Sagban, Sebouh Setrakian, Alberto Rubio-Tapia\",\"doi\":\"10.14309/crj.0000000000001800\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Protein-losing enteropathy (PLE) results in the abnormal loss of proteins through the gastrointestinal tract, leading to malabsorption and hypoalbuminemia. A rare etiology of PLE is Waldenström macroglobulinemia (WM), a hematological malignancy characterized by immunoglobulin M (IgM) monoclonal gammopathy. We present a case of a 66-year-old man with a history of small bowel bacterial overgrowth and lactose intolerance, admitted for worsening gastrointestinal symptoms, including abdominal discomfort, bloating, and watery diarrhea. He had experienced significant weight loss and anasarca over 6 months. Laboratory tests indicated hypoproteinemia, hypoalbuminemia, and elevated IgM levels, accompanied by abnormal stool studies. Imaging showed no significant findings, while endoscopic evaluation revealed lymphangiectasia-like changes in the small bowel. Biopsy results demonstrated proteinaceous material in dilated villi and IgM deposition. The diagnosis of WM was confirmed by bone marrow biopsy. Thus, WM should be considered when evaluating unexplained PLE, particularly with associated gastrointestinal symptoms and elevated IgM levels.</p>\",\"PeriodicalId\":7394,\"journal\":{\"name\":\"ACG Case Reports Journal\",\"volume\":\"12 8\",\"pages\":\"e01800\"},\"PeriodicalIF\":0.5000,\"publicationDate\":\"2025-08-04\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12321444/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACG Case Reports Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.14309/crj.0000000000001800\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2025/8/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q4\",\"JCRName\":\"GASTROENTEROLOGY & HEPATOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACG Case Reports Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.14309/crj.0000000000001800","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/8/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"GASTROENTEROLOGY & HEPATOLOGY","Score":null,"Total":0}
An Extremely Rare Cause of Protein-Losing Enteropathy: Waldenström Macroglobulinemia.
Protein-losing enteropathy (PLE) results in the abnormal loss of proteins through the gastrointestinal tract, leading to malabsorption and hypoalbuminemia. A rare etiology of PLE is Waldenström macroglobulinemia (WM), a hematological malignancy characterized by immunoglobulin M (IgM) monoclonal gammopathy. We present a case of a 66-year-old man with a history of small bowel bacterial overgrowth and lactose intolerance, admitted for worsening gastrointestinal symptoms, including abdominal discomfort, bloating, and watery diarrhea. He had experienced significant weight loss and anasarca over 6 months. Laboratory tests indicated hypoproteinemia, hypoalbuminemia, and elevated IgM levels, accompanied by abnormal stool studies. Imaging showed no significant findings, while endoscopic evaluation revealed lymphangiectasia-like changes in the small bowel. Biopsy results demonstrated proteinaceous material in dilated villi and IgM deposition. The diagnosis of WM was confirmed by bone marrow biopsy. Thus, WM should be considered when evaluating unexplained PLE, particularly with associated gastrointestinal symptoms and elevated IgM levels.
期刊介绍:
ACG Case Reports Journal is a peer-reviewed, open-access publication that provides GI and hepatology fellows, private practice clinicians, and other healthcare providers an opportunity to share interesting case reports with their peers and with leaders in the field. ACG Case Reports Journal publishes case reports, images, videos and letters to the editor in all topics of gastroenterology and hepatology, including: Biliary Colon Endoscopy Esophagus Functional Bowel Disorders Inflammatory Bowel Disease Liver Nutrition and Obesity Pancreas Pathology Pediatric Small Bowel Stomach.