[Pulmonary capillary hemangiomatosis: a clinicopathologic analysis of 2 cases with review of literature].
Department of Pathology, Beijing Chaoyang Hospital, Capital Medical University, Beijing 100020, China.
- Published Article
Zhonghua bing li xue za zhi = Chinese journal of pathology
- Publication Date
Jan 01, 2012
PCH is a rare vascular proliferative disease of yang patients. Increased number of mast cell and the up-regulation of PDGFR-β may suggest mechanism for PCH. The clinical and radiologic diagnosis of PCH can be very difficult, and the histological examination is regarded as the most reliable means to establish the diagnosis. Pathologists should improve their knowledge on PCH.
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This record was last updated on 04/18/2018 and may not reflect the most current and accurate biomedical/scientific data available from NLM.
The corresponding record at NLM can be accessed at https://www.ncbi.nlm.nih.gov/pubmed/22455844