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Recognition of Epidermal Transglutaminase by IgA and Tissue Transglutaminase 2 Antibodies in a Rare Case of Rhesus Dermatitis
Published on: December 15, 2011
Celiac disease, an autoimmune disorder triggered by gluten, can present with diverse symptoms, including bone disease. This case highlights late diagnosis in a 58-year-old due to non-classical signs like pathological fractures.
Area of Science:
- Gastroenterology and Immunology
- Endocrinology and Metabolism
Background:
- Celiac disease is a prevalent autoimmune disorder affecting genetically susceptible individuals upon gluten ingestion.
- It affects approximately 1% of the population, with a higher incidence in women, and is a significant cause of malabsorption.
- Manifestations range from asymptomatic cases to severe malabsorption syndrome, with extraintestinal symptoms common in adults.
Observation:
- This case report details a 58-year-old patient diagnosed with celiac disease at an advanced age.
- The diagnosis was prompted by non-classical symptoms, specifically multiple pathological fractures.
- These fractures stemmed from metabolic bone disease secondary to malabsorption of calcium and vitamin D, leading to hyperparathyroidism.
Findings:
- The gold standard for celiac disease diagnosis involves detecting tissue transglutaminase IgA antibodies and confirming histological findings from a duodenal biopsy.
- This patient's late diagnosis underscores the varied clinical presentations of celiac disease.
- Non-classical symptoms, such as metabolic bone disease and secondary hyperparathyroidism, can be key indicators.
Implications:
- A lifelong gluten-free diet is the established causal treatment for celiac disease.
- Strict adherence to a gluten-free diet is crucial for mitigating serious complications like intestinal T-cell lymphoma.
- This case emphasizes the importance of considering celiac disease in adults presenting with unexplained metabolic bone disease and malabsorption, even in the absence of typical gastrointestinal symptoms.
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