Diffuse pulmonary lymphangiomatosis: a case report with literature review

被引:17
|
作者
Du Ming-hua [1 ,4 ]
Ye Ruan-jian [1 ]
Sun Kun-kun [2 ]
Li Jian-feng [3 ]
Shen Dan-hua [4 ]
Wang Jun [3 ]
Gao Zhan-cheng [1 ]
机构
[1] Beijing Univ, Peoples Hosp, Dept Resp & Crit Care Med, Beijing 100044, Peoples R China
[2] Beijing Univ, Peoples Hosp, Dept Pathol, Beijing 100044, Peoples R China
[3] Beijing Univ, Peoples Hosp, Dept Thorac Surg, Beijing 100044, Peoples R China
[4] Fengning Cty Hosp, Dept Internal Med, Fengning 068350, Hebei, Peoples R China
关键词
diffuse pulmonary lymphangiomatosis; computer tomography; bronchoscopy; DISSEMINATED INTRAVASCULAR COAGULATION; OF-THE-LITERATURE; GENERALIZED LYMPHANGIOMATOSIS; THORACIC LYMPHANGIOMATOSIS; CHYLOTHORAX; CT;
D O I
10.3760/cma.j.issn.0366-6999.2011.05.033
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Diffuse pulmonary lymphangiomatosis (DPL) is a rare disease that is characterized by diffuse proliferation of abnormal pulmonary lymphatic channels. DPL occurs mostly in children and young adults and often undergoes a progressive clinical course, eventually causing deterioration of the lung. Both the clinical diagnosis and treatment of DPL remain a challenge. Here, we report a case of DPL in a 53-year-old Chinese woman with comprehensive investigations including pulmonary function tests, computer tomography (CT), bronchoscopy and histological examination of the lung biopsy, and review the literature. Chin Med J 2011;124(5):797-800
引用
收藏
页码:797 / 800
页数:4
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