Pulmonary capillary hemangiomatosis and hypertrophic cardiomyopathy in a Persian cat
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Updated: Feb 25, 2026

Investigating the Pathogenesis of MYH7 Mutation Gly823Glu in Familial Hypertrophic Cardiomyopathy using a Mouse Model
Published on: August 8, 2022
Tiffany L Jenkins1, Ryan N Jennings1
1Department of Veterinary Biosciences, College of Veterinary Medicine, The Ohio State University, Columbus, OH.
Insights
A rare feline lung condition, pulmonary capillary hemangiomatosis (PCH), was identified post-mortem in a Persian cat. This vascular lung disease, PCH, was associated with hypertrophic cardiomyopathy but not its direct cause.
Area of Science:
- Veterinary Pathology
- Cardiovascular Pathology
- Pulmonary Hypertension
Background:
- Pulmonary capillary hemangiomatosis (PCH) and pulmonary veno-occlusive disease (PVOD) are rare causes of primary pulmonary hypertension in humans.
- These conditions were first reported in dogs in 2016.
- A case of PCH in a cat is presented.
Abstract:
Pulmonary capillary hemangiomatosis (PCH) and pulmonary veno-occlusive disease (PVOD) are rare causes of primary pulmonary hypertension in humans, and, in 2016, were reported in dogs. A 1-y-old, neutered male Persian cat was presented for autopsy after sudden death several hours after grooming. Grossly, the lungs were mottled red-to-pink, contained rubbery-to-firm nodular foci, and there was moderate-to-marked left-sided cardiomegaly and left atrial dilation, consistent with hypertrophic cardiomyopathy. Microscopically, there was multifocal to regionally extensive capillary proliferation within pulmonary alveolar septa and around respiratory bronchioles, with nodular aggregates of densely arranged capillaries that replaced pulmonary alveolar spaces. Rare occlusive venous remodeling was identified in Verhoeff-van Gieson-stained sections. The gross and microscopic changes were consistent with PCH with rare features of PVOD. Hypertrophic cardiomyopathy was interpreted as potentially contributing to the cause of death, but unrelated to the pulmonary vascular proliferation.
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