Chermiti Ben Abbdallah Fatma , Chtourou Amel , Mahouchi Ridha , Smaïl Olfa , Taktak Sophia , Mezni Faouzi , Ben Kheder Ali
{"title":"成人特发性肺含铁血黄素沉着症","authors":"Chermiti Ben Abbdallah Fatma , Chtourou Amel , Mahouchi Ridha , Smaïl Olfa , Taktak Sophia , Mezni Faouzi , Ben Kheder Ali","doi":"10.1016/j.rmedc.2009.10.004","DOIUrl":null,"url":null,"abstract":"<div><p>Idiopathic pulmonary hemosiderosis (IPH) is a rare unknown origin disease characterized by diffuse alveolar hemorrhage (DPH). It rarely occurs in adults. We report a case of 50-year-old man, hospitalized with acute respiratory insuffiency. The chest radiograph and computed tomography scan showed bilateral interstitial and ground-glass opacities. The diagnosis of IPH was confirmed by broncho-alveolar lavage (BAL) and surgical pulmonary biopsy. There was no sign of capillaritis or granuloma in the anatomopathologic study. No remission was obtained after two months of high-dose corticosteroid therapy</p></div>","PeriodicalId":89478,"journal":{"name":"Respiratory medicine CME","volume":"3 4","pages":"Pages 238-240"},"PeriodicalIF":0.0000,"publicationDate":"2010-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.10.004","citationCount":"5","resultStr":"{\"title\":\"Idiopathic pulmonary hemosiderosis in adult\",\"authors\":\"Chermiti Ben Abbdallah Fatma , Chtourou Amel , Mahouchi Ridha , Smaïl Olfa , Taktak Sophia , Mezni Faouzi , Ben Kheder Ali\",\"doi\":\"10.1016/j.rmedc.2009.10.004\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>Idiopathic pulmonary hemosiderosis (IPH) is a rare unknown origin disease characterized by diffuse alveolar hemorrhage (DPH). It rarely occurs in adults. We report a case of 50-year-old man, hospitalized with acute respiratory insuffiency. The chest radiograph and computed tomography scan showed bilateral interstitial and ground-glass opacities. The diagnosis of IPH was confirmed by broncho-alveolar lavage (BAL) and surgical pulmonary biopsy. There was no sign of capillaritis or granuloma in the anatomopathologic study. No remission was obtained after two months of high-dose corticosteroid therapy</p></div>\",\"PeriodicalId\":89478,\"journal\":{\"name\":\"Respiratory medicine CME\",\"volume\":\"3 4\",\"pages\":\"Pages 238-240\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2010-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.1016/j.rmedc.2009.10.004\",\"citationCount\":\"5\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Respiratory medicine CME\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S1755001709000980\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Respiratory medicine CME","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S1755001709000980","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Idiopathic pulmonary hemosiderosis (IPH) is a rare unknown origin disease characterized by diffuse alveolar hemorrhage (DPH). It rarely occurs in adults. We report a case of 50-year-old man, hospitalized with acute respiratory insuffiency. The chest radiograph and computed tomography scan showed bilateral interstitial and ground-glass opacities. The diagnosis of IPH was confirmed by broncho-alveolar lavage (BAL) and surgical pulmonary biopsy. There was no sign of capillaritis or granuloma in the anatomopathologic study. No remission was obtained after two months of high-dose corticosteroid therapy
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