Ouattara Khadidia, Kanouté Tenin, Baya Bocar, S. Dianguina, Kamian Youssouf Mama, S. Youssouf, Fofana Aminata, Traoré Mohamed Maba, Guindo Ibrahim, Sidibe Fatoumata, Dakouo Aimé Paul, S. F. Bintou, Bamba Salimata, Coulibaly Lamine, Yossi Oumar, Koné Samba, T. Yacouba
{"title":"Pulmonary Hypoplasia: A Rare Cause of Chronic Cough in TB Endemic Area","authors":"Ouattara Khadidia, Kanouté Tenin, Baya Bocar, S. Dianguina, Kamian Youssouf Mama, S. Youssouf, Fofana Aminata, Traoré Mohamed Maba, Guindo Ibrahim, Sidibe Fatoumata, Dakouo Aimé Paul, S. F. Bintou, Bamba Salimata, Coulibaly Lamine, Yossi Oumar, Koné Samba, T. Yacouba","doi":"10.4236/OJRD.2019.91002","DOIUrl":null,"url":null,"abstract":"Pulmonary hypoplasia is a rare disease characterized by a defect of lung development more often unilateral. The diagnosis requires several exams to eliminate other causes of pulmonary retraction. We report two cases at the department of pneumophtisiology of the University Teaching Hospital of Point G. The first case is a young adult who was complaining of a chronic cough. Etiological investigation required several exams including spirometry and Computed tomographic scan (CT scan). After elimination of all suspected causes of pulmonary opacity, the diagnosis of pulmonary hypoplasia was retained. The second case is a 2-year-old girl who was born with congenital cardiopathy whose respiratory complications were increasing during her childhood and respiratory explorations discovered pulmonary agenesis. Pulmonary hypoplasia is rare in our medical practice, but attention must be drawn to a retractile pulmonary opacity in young age after elimination of all infectious causes in TB endemic area.","PeriodicalId":83134,"journal":{"name":"The Journal of respiratory diseases","volume":"9 1","pages":"18-25"},"PeriodicalIF":0.0000,"publicationDate":"2019-01-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"The Journal of respiratory diseases","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.4236/OJRD.2019.91002","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
Abstract
Pulmonary hypoplasia is a rare disease characterized by a defect of lung development more often unilateral. The diagnosis requires several exams to eliminate other causes of pulmonary retraction. We report two cases at the department of pneumophtisiology of the University Teaching Hospital of Point G. The first case is a young adult who was complaining of a chronic cough. Etiological investigation required several exams including spirometry and Computed tomographic scan (CT scan). After elimination of all suspected causes of pulmonary opacity, the diagnosis of pulmonary hypoplasia was retained. The second case is a 2-year-old girl who was born with congenital cardiopathy whose respiratory complications were increasing during her childhood and respiratory explorations discovered pulmonary agenesis. Pulmonary hypoplasia is rare in our medical practice, but attention must be drawn to a retractile pulmonary opacity in young age after elimination of all infectious causes in TB endemic area.