Jiang Maolin, Li Hongbo, Song Jishuo, et al. Preliminary Study on Lung Function Damage in Children with Congenital Lung Cystic Lesions. [J]. 26(2):7-10(2020)
DOI:
Jiang Maolin, Li Hongbo, Song Jishuo, et al. Preliminary Study on Lung Function Damage in Children with Congenital Lung Cystic Lesions. [J]. 26(2):7-10(2020) DOI: 10.13407/j.cnki.jpp.1672-108X.2020.02.003.
Preliminary Study on Lung Function Damage in Children with Congenital Lung Cystic Lesions
Objective: To probe into the effects of congenital lung cystic lesions on children’s lung function
so as to provide reference for clinical surgical treatment. Methods: From Jan. 2014 to Sept. 2018
totally 49 children diagnosed with congenital lung cystic lesions in Children’s Hospital of Chongqing Medical University were extracted
preoperative lung function was measured and statistically analyzed. Among them
23 children were <42 months
and the lung function was measured by tidal breathing method; 26 children were ≥42 months
and the lung function was measured by conventional ventilation method. Results: There were 18 cases (36.8%) of bronchogenic cysts (BC)
among which 5 cases (<42 months) had abnormalities in TPTEF/TE
VPEF/VE
PF/V25 and TI/TE
indicating moderate obstruction of small airway and mild obstruction of large airway; and 7 cases (≥42 months) had abnormalities in FVC
FEV1
FEF75 and MMEF
suggesting mild mixed ventilation dysfunction. There were 15 cases (30.6)% of congenital cystic adenomatoid malformation (CCAM)
among which 8 cases (<42 months) had abnormalities in TPTEF/TE
PF/V25 and TI/TE
suggesting mild obstruction of large and small airway; 7 cases (≥42 months) had normal lung function. There were 10 cases (20.4%) of pulmonary sequestration (PS)
among which 7 cases (<42 months) had abnormalities in TEF50/TIF50 and TI/TE
suggesting mild obstruction of large airway; 3 cases (≥42 months) had normal lung function. There were 6 cases (12.2%) of congenital lobar emphysema (CLE)
among which 3 cases (<42 months) had abnormalities in TPTEF/TE
VPEF/VE
PF/V25
TEF50/TIF50 and TI/TE
suggesting moderate obstruction of small airway and mild obstruction of large airway; 3 cases (≥42 months) had normal lung function. In terms of clinical manifestations
11 cases (47.8%) in the <42-month group had the history of lung infection
and 20 cases (76.9%) in the ≥42-month group had the history of lung infection. Conclusion: Congenital lung cystic lesions causes lung function impairment in children
mainly manifested by airway dysfunction at different degree. The degree of impairment of lung function is more obvious in younger age groups
and older age groups are more prone to have repeated lung infections. Early surgery is the preferred treatment option.
关键词
儿童先天性肺囊性疾病肺功能
Keywords
childrencongenital lung cystic lesionslung function
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