Pulmonary pneumocytoma

Pulmonary pneumocytomas, previously known as pulmonary sclerosing hemangiomas (PSH), are rare benign neoplasms of the lung.

Typically presents in middle age (30-50 years of age). There is a recognized female predilection. 

Most patients are asymptomatic. Symptoms if present will include hemoptysis, cough, chest pain (maybe pleuritic) and breathlessness.

It is a rare benign tumor which is microscopically characterized by four main histological components (solid, papillary, sclerotic, and hemangiomatous) 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

It was first described by A A Leibow and D S Hubell et al. in 1956 3.


Article information

rID: 11119
System: Oncology, Chest
Tag: cases, cases
Synonyms or Alternate Spellings:
  • Pulmonary sclerosing haemangioma (PSH)
  • Pulmonary sclerosing hemangioma
  • Sclerosing hemangioma of lung
  • Papillary pneumocytoma
  • Pulmonary sclerosing haemangiomas
  • Pulmonary sclerosing hemangiomas
  • Pneumoctyoma of lung
  • Pulmonary sclerosing haemangioma
  • Pulmonary sclerosing pneumocytoma

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Cases and figures

  • Case 1: adjacent to right hilum
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