K Kodama, M Hamada, Y Shigematsu, M Suzuki, K Hiwada, Y Hayashi, H Hashimoto, H Hashimoto, A Sugita
{"title":"家族性原发性肺动脉高压——两个兄弟姐妹的报告。","authors":"K Kodama, M Hamada, Y Shigematsu, M Suzuki, K Hiwada, Y Hayashi, H Hashimoto, H Hashimoto, A Sugita","doi":"10.2169/internalmedicine1962.30.273","DOIUrl":null,"url":null,"abstract":"<p><p>Familial primary pulmonary hypertension was found in two siblings (sister and brother). The woman noted exertional dyspnea at the age of 28 yr. The younger brother noticed exertional dyspnea, cough with bloody sputum and pretibial edema at the age of 38 yr. We diagnosed them as primary pulmonary hypertension as based on hemodynamic and histopathological findings. Regardless of the treatment, both patients died of right-sided heart failure with a short time course. We examined their family members, but there were no other members with primary pulmonary hypertension.</p>","PeriodicalId":14798,"journal":{"name":"Japanese journal of medicine","volume":"30 3","pages":"273-7"},"PeriodicalIF":0.0000,"publicationDate":"1991-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.2169/internalmedicine1962.30.273","citationCount":"2","resultStr":"{\"title\":\"Familial primary pulmonary hypertension--report of two siblings.\",\"authors\":\"K Kodama, M Hamada, Y Shigematsu, M Suzuki, K Hiwada, Y Hayashi, H Hashimoto, H Hashimoto, A Sugita\",\"doi\":\"10.2169/internalmedicine1962.30.273\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Familial primary pulmonary hypertension was found in two siblings (sister and brother). The woman noted exertional dyspnea at the age of 28 yr. The younger brother noticed exertional dyspnea, cough with bloody sputum and pretibial edema at the age of 38 yr. We diagnosed them as primary pulmonary hypertension as based on hemodynamic and histopathological findings. Regardless of the treatment, both patients died of right-sided heart failure with a short time course. We examined their family members, but there were no other members with primary pulmonary hypertension.</p>\",\"PeriodicalId\":14798,\"journal\":{\"name\":\"Japanese journal of medicine\",\"volume\":\"30 3\",\"pages\":\"273-7\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1991-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://sci-hub-pdf.com/10.2169/internalmedicine1962.30.273\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Japanese journal of medicine\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.2169/internalmedicine1962.30.273\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Japanese journal of medicine","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.2169/internalmedicine1962.30.273","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Familial primary pulmonary hypertension--report of two siblings.
Familial primary pulmonary hypertension was found in two siblings (sister and brother). The woman noted exertional dyspnea at the age of 28 yr. The younger brother noticed exertional dyspnea, cough with bloody sputum and pretibial edema at the age of 38 yr. We diagnosed them as primary pulmonary hypertension as based on hemodynamic and histopathological findings. Regardless of the treatment, both patients died of right-sided heart failure with a short time course. We examined their family members, but there were no other members with primary pulmonary hypertension.