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Updated: Sep 25, 2025

Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Updates on the diagnosis and management of celiac disease
Kristina Soltesz1, Jessica Mosebach, Emily Paruch
1At the time this article was written, Kristina Soltesz, Jessica Mosebach , and Emily Paruch were students in the PA program at Pace University-Lenox Hill Hospital in New York City, N.Y. Ms. Soltesz now practices in neurosurgery at Lenox Hill Hospital, Ms. Mosebach practices at St. Luke's University Health Network in Easton, Pa., and Ms. Paruch practices at Northwell GoHealth Urgent Care in New York City. Jean Covino is chair of the PA program at Pace University-Lenox Hill Hospital. The authors have disclosed no potential conflicts of interest, financial or otherwise.
Abstract:
Celiac disease is a chronic autoimmune enteropathy affecting about 1% of the population. Gluten ingestion triggers an immune response in genetically susceptible patients, resulting in intestinal and extraintestinal disease manifestations. Current recommendations for diagnosis include serology for celiac-specific antibodies to transglutaminase, endomysium, and deamidated gliadin, and IgA serology. New highly accurate point-of-care tests can efficiently screen for celiac disease and improve the diagnostic timeframe. Definitive diagnosis is most commonly made via biopsy of the small bowel showing villous atrophy. A gluten-free diet with micronutrient supplementation is the only recommended treatment for celiac disease. Primary care providers must be able to recognize screening indications, refer patients appropriately, and provide proper patient education and follow-up.
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