Pulmonary pneumocytomas, previously known as pulmonary sclerosing haemangiomas (PSH), also known as are rare benign neoplasms of the lung.
Typically presents in middle age (30-50 years of age). There is a recognised female predilection.
Most patients are asymptomatic. Symptoms if present will include haemoptysis, cough, chest pain, dyspnea, and pleurisy.
It is a rare benign tumor which is microscopically characterized by four main histological components (solid, papillary, sclerotic, and haemangiomatous) in varying proportions. A thin fibrous pseudocapsule separates it from the adjacent compressed lung parenchyma.
There can be significant size variability where the lesions range from 1~8 cm in diameter, although most are < 3.5 cm.
- they usually tend to present as a solitary, well-defined nodular lesion (oval to rounded shadow).
- they occasionally contain areas of calcification
- may show an air-meniscus sign: crescentic radiolucency at the periphery of a lung nodule 4
- often seen as a well defined intraparechymal nodular mass (often juxta-pleural)
- areas of calcification may be present
- may show a radiolucent zone around the lesion 5
- shows significant but inhomogeneous enhancement 2,8
History and etymology
It was first described by A A Leibow and D S Hubell et.al in 1956 3.
lung cancer: overview
non small-cell lung cancer
- adenosquamous carcinoma
- large cell carcinoma
- primary sarcomatoid carcinoma of lung
- squamous cell carcinoma
- salivary gland type tumours
- pulmonary neuroendocrine tumours
- preinvasive lesions
- benign neoplasms
- pulmonary metastases
- lung cancer screening
- lung cancer staging
- non small-cell lung cancer
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- 9. Wang QB, Chen YQ, Shen JJ et-al. Sixteen cases of pulmonary sclerosing haemangioma: CT findings are not definitive for preoperative diagnosis. Clin Radiol. 2011;66 (8): 708-14. doi:10.1016/j.crad.2011.03.002 - Pubmed citation
- 10. Baysak A, Oz AT, Moğulkoç N et-al. A rare tumor of the lung: pulmonary sclerosing hemangioma (pneumocytoma). Respir Med. 2013;107 (3): 448-50. doi:10.1016/j.rmed.2012.12.005 - Pubmed citation