scholarly journals Concurrent bronchopulmonary foregut malformations: a rare case of right-sided extralobar pulmonary sequestration and bronchogenic cyst

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.

2006 ◽  
Vol 22 (1) ◽  
pp. 89-89
Author(s):  
S Nagarajan ◽  
R Santosham ◽  
R Santosham ◽  
RK Sashankh ◽  
R Santosham

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 ◽  
...  

2016 ◽  
Vol 04 (01) ◽  
pp. 010-012 ◽  
Author(s):  
Mario Lima ◽  
Michela Maffi ◽  
Tommaso Gargano ◽  
Giovanni Ruggeri ◽  
Michele Libri ◽  
...  

We report the case of a neonate affected by prenatally diagnosed congenital diaphragmatic hernia (CDH), treated by thoracoscopy. During the procedure, we detected an associated extralobar pulmonary sequestration (EPS), which was preoperatively undiagnosed, and we removed it. EPS has been shown to be associated with CDH in up to 15 to 40% of cases. A possible explanation hypothesized is that pulmonary sequestration, which develops at 4 to 5 weeks of gestation, can disturb the fusion of the diaphragm and closure of the pleuroperitoneal canal. The thoracoscopic approach permitted us to identify the thoracic EPS that probably would have been otherwise missed.


2015 ◽  
Vol 14 (1) ◽  
pp. 26-31
Author(s):  
N. A. Ilina ◽  
I. E. Myagkova

Relevance. Pulmonary sequestrations are rare pathology and make from 0.15 to 6.4 % of all congenital abnormality. Thus intra-abdominal localization of this malformation is described only in 2.5 % of all pulmonary sequestrations. Objective. Reflect the difficulty of differential diagnosis of rare lung malformation in newborns. Materials and methods. 2 cases of the extralobar sequestration located under the diaphragm diagnosed for newborns in a children's hospital for the last 20 years are in details described. Results. The diagnosis of an intra-abdominal extralobular pulmonary sequestration was finalized only after surgical treatment, confirmed histologically. Questions of differential diagnostics of rare congenital pulmonary malformations are discussed with tumors of suprarenal localization at newborns, comparison of own results to data of literature. Conclusions. In the differential diagnosis of suprarenal lesions at newborns it is necessary to consider the possibility of intra-abdominal extralobar pulmonary sequestration, especially in the localization of pathological changes at the left side.


Open Medicine ◽  
2016 ◽  
Vol 11 (1) ◽  
pp. 200-203
Author(s):  
Francesco Molinaro ◽  
Rossella Angotti ◽  
Alfredo Garzi ◽  
Vincenzo Giuseppe Di Crescenzo ◽  
Antonio Cortese ◽  
...  

AbstractCongenital cystic lung lesions are a rare but clinically significant group of anomalies, including congenital cystic adenomatoid malformation (CCAM), pulmonary sequestration, congenital lobar emphysema (CLE) and bronchogenic cysts. Despite the knowledge of these lesions increasing in the last years, some aspects are still debated and controversial. The diagnosis is certainly one aspect which underwent many changes in the last 15 years due to the improvement of antenatal scan and the introduction of 3-D reconstruction techniques. As it is known, a prompt diagnosis has an essential role in the management of these children. The new imaging studies as 3D Volume rendering system are the focus of this paper. We describe our preliminary experience in a case of hybrid lung lesion, which we approached by thoracoscopy after a preoperative study with 3D VR reconstruction. Our final balance is absolutely positive.


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

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