Pulmonary Hypoplasia: A Rare Cause of Chronic Cough in TB Endemic Area

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
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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.
肺发育不全:结核病流行地区慢性咳嗽的罕见病因
肺发育不全是一种罕见的疾病,其特征是肺发育缺陷,通常为单侧。诊断需要多次检查以消除肺回缩的其他原因。我们报告了G点大学教学医院肺组织生物学科的两例病例。第一例是一名年轻人,他抱怨慢性咳嗽。病因调查需要进行多项检查,包括肺活量测定和计算机断层扫描(CT扫描)。在排除了所有怀疑的肺部混浊原因后,保留了对肺部发育不全的诊断。第二个病例是一名2岁女孩,她出生时患有先天性心脏病,其呼吸道并发症在童年时期不断增加,呼吸探查发现肺部发育不全。肺发育不全在我们的医疗实践中是罕见的,但在结核病流行地区消除所有感染原因后,必须注意年轻时可伸缩的肺混浊。
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