cystic lung lesion
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Author(s):  
Carolyn Hanna ◽  
Priya G. Sharma ◽  
Moiz M. Mustafa ◽  
Jennifer Reppucci ◽  
Archana Shenoy ◽  
...  

Abstract Background Bronchopulmonary foregut malformations are rare congenital malformations. It is extremely rare to have malformations that occur simultaneously. There is literature to show that extralobar sequestration is associated with other congenital anomalies, most commonly diaphragmatic hernias, and also with other bronchopulmonary foregut malformations (e.g., extralobar sequestration and congenital pulmonary airway malformations). However, very few case reports were found that reported extralobar sequestration and foregut duplication cysts and only one report of a right-sided complex foregut malformation with pulmonary sequestration. Case presentation We present a case of a 3-month-old male infant with a prenatal diagnosis of a cystic lung lesion who, after developing symptoms of respiratory distress, was found to have concurrent right-sided extralobar pulmonary sequestration and a mediastinal bronchogenic cyst. Conclusions The concurrent occurrence of these malformations in one patient could help support the theory that these malformations result from an early error in development during the time when both the lung buds and foregut are developing simultaneously.


2019 ◽  
Vol 82 (2) ◽  
pp. 226-227
Author(s):  
Salih Bilen ◽  
Celal Buğra Sezen ◽  
Celalettin Ibrahim Kocaturk

2018 ◽  
Vol 10 (11) ◽  
pp. 6230-6237
Author(s):  
Hui Wang ◽  
Feng-Hua Wang ◽  
Jian-Hua Liang ◽  
Wei Liu ◽  
Jing-Zhou Yang ◽  
...  

ASVIDE ◽  
2018 ◽  
Vol 5 ◽  
pp. 865-865
Author(s):  
Hui Wang ◽  
Feng-Hua Wang ◽  
Jian-Hua Liang ◽  
Wei Liu ◽  
Jing-Zhou Yan ◽  
...  

2018 ◽  
Vol 10 (11) ◽  
pp. 6230-6237
Author(s):  
Hui Wang ◽  
Feng-Hua Wang ◽  
Jian-Hua Liang ◽  
Wei Liu ◽  
Jing-Zhou Yang ◽  
...  

CHEST Journal ◽  
2016 ◽  
Vol 150 (4) ◽  
pp. 818A
Author(s):  
Zeeshan Solangi ◽  
Saad Qadwai ◽  
Lakshmi Asritha Gollapudi ◽  
Pratik Mondal ◽  
Srikanth Yandrapalli ◽  
...  

2016 ◽  
Vol 26 (2) ◽  
pp. 121-124
Author(s):  
Eman Sobh ◽  
Amira Bahour ◽  
Shady Elia Anis

Congenital cystic adenomatoid malformation (CCAM) – recently reported as congenital pulmonary airway malformation – is a rare abnormality of lung development. We present a case of a six-year-old child having a cystic lung lesion that proved to be CCAM after surgical resection. The child is performing well on follow-up.


2015 ◽  
Vol 10 (1) ◽  
pp. 41-42
Author(s):  
Asish Banerjee ◽  
Sumita Pal ◽  
Anish Chatterjee ◽  
A Pan

A term neonate developed respiratory distress after 12 hours of birth which was diagnosed as a case of congenital cystic adenomatoid malformation (CCAM) of the right lung by computerized tomography scan. CCAM of the lung is rare congenital cystic lung lesion. DOI: http://dx.doi.org/10.3126/jcmsn.v10i1.12767 Journal of College of Medical Sciences-Nepal, 2014, Vol.10(1); 41-42


CHEST Journal ◽  
2010 ◽  
Vol 138 (1) ◽  
pp. 208-212 ◽  
Author(s):  
Ryu Ehara ◽  
Takeharu Koga ◽  
Koichi Higaki ◽  
Kiminori Fujimoto ◽  
Takamichi Mitsutake

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