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[Pulmonary capillary hemangiomatosis: a clinicopathologic analysis of 2 cases with review of literature].

Authors
Type
Published Article
Journal
Zhonghua bing li xue za zhi Chinese journal of pathology
Publication Date
Volume
41
Issue
1
Pages
16–19
Identifiers
PMID: 22455844
Source
Medline

Abstract

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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