Lane-Hamilton syndrome - Is it really a needle in a haystack?
S A Mondkar1, M S Tullu1, P Sathe2
1Department of Pediatrics, Seth G.S. Medical College and KEM Hospital, Parel, Mumbai, Maharashtra, India.
Journal of Postgraduate Medicine
|October 28, 2021
Summary
Pulmonary hemosiderosis, a rare complication of celiac disease, can cause anemia and lung infiltrates. Treatment with a strict gluten-free diet and steroids effectively resolved symptoms in a pediatric case.
Area of Science:
- Pediatric Gastroenterology
- Pulmonology
- Hematology
Background:
- Celiac disease is an autoimmune disorder triggered by gluten ingestion.
- Pulmonary hemosiderosis, characterized by iron deposition in the lungs, is a rare manifestation of celiac disease.
- Lane-Hamilton syndrome describes the association between celiac disease and pulmonary hemosiderosis.
Observation:
- A 5-year-old girl presented with anemia, fever, cough, and breathlessness.
- Initial investigations revealed dimorphic anemia and high anti-tissue transglutaminase IgA antibodies, confirming celiac disease.
- Persistent pulmonary infiltrates, initially misdiagnosed as congestive cardiac failure, led to further investigation.
Findings:
- High-resolution computed tomography (HRCT) showed interstitial thickening and alveolar shadows.
- Lung biopsy confirmed extensive pulmonary hemosiderosis.
- Treatment with a gluten-free diet and oral steroids resulted in complete resolution of anemia and pulmonary infiltrates.
Implications:
- Pulmonary hemosiderosis should be considered in celiac disease patients with unexplained anemia and respiratory symptoms.
- Early diagnosis and strict adherence to a gluten-free diet are crucial for managing this rare complication.
- This case highlights the importance of a multidisciplinary approach in diagnosing and treating complex pediatric cases.
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