Pulmonary capillary hemangiomatosis: An unusual cause of primary pulmonary hypertension in a child with characteristic computed tomography imaging features

被引：3

作者：

Manjubashini, D. ^{[1
]}

Nagarajan, K. ^{[1
]}

Kumar, B. Rajesh ^{[2
]}

机构：

[1] Jawaharlal Inst Postgrad Med Educ & Res, Dept Radiodiag, Pondicherry 600506, India

[2] Jawaharlal Inst Postgrad Med Educ & Res, Dept Pulm Med, Pondicherry, India

来源：

LUNG INDIA | 2019年 / 36卷 / 02期

关键词：

Multidetector computed tomography; primary pulmonary hypertension; pulmonary capillary hemangiomatosis; THIN-SECTION CT;

D O I：

10.4103/lungindia.lungindia_122_18

中图分类号：

R56 [呼吸系及胸部疾病];

学科分类号：

摘要：

Pulmonary capillary hemangiomatosis (PCH) is a rare cause of primary pulmonary hypertension (PPH) diagnosed in children and young adults with a nonspecific clinical presentation of dyspnea, cough, chest pain, and fatigue. It is characterized by extensive proliferation of pulmonary capillaries within alveolar septa. The imaging features include diffuse centrilobular ground-glass opacities with features of pulmonary hypertension. We present a case of PCH in an 11-year-old boy who was diagnosed with PPH in echocardiography and referred for diagnostic imaging.

引用

页码：157 / 159

页数：3

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