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Aims: The aim is to assess the usefulness of routine duodenal biopsy in patients presenting with iron deficiency anemia in areas with low prevalence of celiac disease (CD).
Methods: This prospective study included 156 patients with unexplained iron deficiency anemia, referred to the Department of Gastroenterology. JSS Medical College and Hospital, Mysuru, India. All patients underwent upper gastrointestinal (GI) endoscopy and duodenal biopsy. Histopathological changes were assessed according to the Marsh classification. Celiac disease was defined as having Marsh II or above on histopathology or being seropositive with Marsh I histopathology and having a good response to gluten-free diet. Furthermore, patients were evaluated for Immunoglobulin A (IgA) anti-tissue transglutaminase (t-TG) antibody with enzyme-linked immunosorbent assay technique.
Results: One hundred and fifty-six patients were included in the study with a mean age of 52.17 ± 16.01 (67.7% of females) who underwent endoscopic duodenal biopsy. Three (1.9%) were diagnosed to have CD on biopsy, which was confirmed with a serological test (IgA Anti t-Tg). Positivity for CD did not correlate with the severity of anemia or GI symptoms.
Conclusions: Celiac disease should be considered in patients presenting with unexplained iron deficiency anemia, even if not accompanied by GI symptoms. Doing initial serological testing followed by duodenal biopsy may be an appropriate approach, especially in areas with a low prevalence of celiac disease. Routine duodenal biopsies did not seem a reasonable approach considering cost-effectiveness and its clinical utility.
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http://dx.doi.org/10.4103/aam.aam_30_25 | DOI Listing |
Dan Med J
August 2025
Department of Hepatology and Gastroenterology, Aarhus University Hospital.
Introduction: A no-biopsy approach has been suggested for diagnosing coeliac disease (CD) in adult patients. This approach is already well established in diagnosing children with CD. This study aimed to evaluate the accuracy of IgA anti-tissue transglutaminase (IgA anti-tTG) in predicting duodenal mucosal lesions diagnostic of CD in adult patients.
View Article and Find Full Text PDFSurg Case Rep
September 2025
Department of Surgery, Graduate School of Medicine, Kyoto University, Kyoto, Kyoto, Japan.
Introduction: von Hippel-Lindau (VHL) disease is an autosomal dominant hereditary disorder characterized by the development of tumor-like lesions in multiple organs. While central nervous system hemangioblastomas, pancreatic neuroendocrine tumors, and pancreatic cysts are commonly associated with VHL disease, there have been few reported cases of pancreatic hemangioblastoma in patients with VHL disease.
Case Presentation: A male patient in his 30s had been diagnosed with VHL disease and had been followed for cerebellar and spinal hemangioblastomas, and renal cell carcinoma, for which he had undergone several tumor resections, radiation therapy, and a ventriculoperitoneal shunt.
Cureus
August 2025
Department of Pediatrics, Mohammed VI University Hospital Center, Oujda, MAR.
We report the case of a nine-year-old boy who presented with severe pancytopenia and respiratory distress. His medical history was notable for pica, chronic epigastric pain, pallor, and intermittent vomiting. Initial laboratory investigations revealed profound anemia (Hemoglobin (Hb) 2 g/dL), neutropenia, thrombocytopenia, and significant deficiencies in vitamin B12 and vitamin D.
View Article and Find Full Text PDFGenes Immun
September 2025
Department of Genetics, University Medical Center Groningen, University of Groningen, Groningen, The Netherlands.
In coeliac disease (CeD), the epithelial lining (EL) of the small intestine is severely damaged by a complex auto-inflammatory response, leading intraepithelial lymphocytes to attack epithelial cells. To understand the intestinal changes and genetic regulation in CeD, we investigated the heterogeneity in the transcriptomic profile of the duodenal EL using RNA-seq and eQTL analysis on predicted cell types. The study included duodenal biopsies from 82 patients, grouped into controls, gluten-free diet treated CeD and untreated CeD.
View Article and Find Full Text PDFHum Pathol
September 2025
Department of Pathology and Cell Biology, Columbia University Irving Medical Center, New York, NY. Electronic address:
Histologic gastric eosinophilia (HGE), characterized by dense eosinophil infiltration in gastric mucosa, is an understudied disease with unclear etiology. Unlike its counterpart, eosinophilic esophagitis (EoE), which has defined diagnostic eosinophil thresholds and characteristic endoscopic findings, proposed eosinophil thresholds for the diagnosis of HGE vary and endoscopic findings are not well characterized. This study aimed to assess the clinical, histological, and endoscopic features of HGE in adults and children.
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