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Indian J Chest Dis Allied Sci · Oct 2014
Case ReportsPulmonary capillary haemangiomatosis: a rare cause of pulmonary hypertension.
- K Anand Babu, K Supraja, and Raj B Singh.
- Indian J Chest Dis Allied Sci. 2014 Oct 1; 56 (4): 259-62.
AbstractPulmonary capillary haemangiomatosis (PCH) is a rare disorder of unknown aetiology, characterised by proliferating capillaries that invade the pulmonary interstitium, alveolar septae and the pulmonary vasculature. It is often mis-diagnosed as primary pulmonary hypertension and pulmonary veno-occlusive disease. Pulmonary capillary haemangiomatosis is a locally aggressive benign vascular neoplasm of the lung. We report the case of a 19-year-old female who was referred to us in the early post-partum period with severe pulmonary artery hypertension, which was diagnosed as PCH by open lung biopsy.
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