{"title":"硬化性肺细胞瘤:一种模拟癌","authors":"Li-cheng Song, Peng Yan, G. Mo","doi":"10.15761/icst.1000352","DOIUrl":null,"url":null,"abstract":"Pulmonary sclerosing pneumocytoma (PSP) is a rare benign neoplasm, predominantly occurring in middle-aged women. When first reported, PSP was thought to be vascular in origin and named pulmonary sclerosing hemangioma because of its high morphological similarity to cutaneous sclerosing hemangioma. Thanks to electron microscopy and immunofluorescence, it has been defined as being primitive respiratory epithelium-oriented and renamed as PSP [1].","PeriodicalId":90850,"journal":{"name":"Integrative cancer science and therapeutics","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2021-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"3","resultStr":"{\"title\":\"Sclerosing Pneumocytoma: A Carcinoma Mimicker\",\"authors\":\"Li-cheng Song, Peng Yan, G. Mo\",\"doi\":\"10.15761/icst.1000352\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Pulmonary sclerosing pneumocytoma (PSP) is a rare benign neoplasm, predominantly occurring in middle-aged women. When first reported, PSP was thought to be vascular in origin and named pulmonary sclerosing hemangioma because of its high morphological similarity to cutaneous sclerosing hemangioma. Thanks to electron microscopy and immunofluorescence, it has been defined as being primitive respiratory epithelium-oriented and renamed as PSP [1].\",\"PeriodicalId\":90850,\"journal\":{\"name\":\"Integrative cancer science and therapeutics\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2021-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"3\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Integrative cancer science and therapeutics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15761/icst.1000352\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Integrative cancer science and therapeutics","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15761/icst.1000352","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Pulmonary sclerosing pneumocytoma (PSP) is a rare benign neoplasm, predominantly occurring in middle-aged women. When first reported, PSP was thought to be vascular in origin and named pulmonary sclerosing hemangioma because of its high morphological similarity to cutaneous sclerosing hemangioma. Thanks to electron microscopy and immunofluorescence, it has been defined as being primitive respiratory epithelium-oriented and renamed as PSP [1].
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