1.
Indian J Ophthalmol
;
2022 Jul; 70(7): 2746-2748
Artigo
| IMSEAR
| ID: sea-224507
2.
Artigo
em Inglês
| IMSEAR
| ID: sea-156806
RESUMO
Pulmonary 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.