Güttinger Eva, Vrugt Bart, Speich Rudolf, Ulrich Silvia, Schwitz Fabienne, Arrigo Mattia, Huber Lars C
Division of Pulmonology, University Hospital Zurich and University of Zurich, 8091 Zurich, Switzerland.
Institute of Surgical Pathology, University Hospital Zurich, 8091 Zurich, Switzerland.
Case Rep Cardiol. 2016;2016:9384126. doi: 10.1155/2016/9384126. Epub 2016 Mar 16.
Pulmonary capillary hemangiomatosis (PCH) is a rare histological substrate within the spectrum of pulmonary arterial hypertension that possibly represents an unusual manifestation of pulmonary veno-occlusive disease (PVOD). One of the histological hallmarks of PCH is the proliferation of pulmonary capillaries in the alveolar septa that infiltrate adjacent structures such as bronchioles, vessels, and visceral pleura. The hyperplastic process involving the smallest vessels of the pulmonary vascular bed might reflect uncontrolled angiogenesis, but whether this vascular proliferation is idiopathic or, conversely, a reactive process remains to be elucidated. Here we discuss the pathogenesis of PCH exemplified by the first reported case of a young patient with repaired scimitar syndrome that developed unilateral PCH.