Surgical Treatment and Its Prognosis for Extralobar Pulmonary Sequestration with Foregut Communication: Communicating Bronchopulmonary Foregut Malformation (CBPFM)

2020 ◽  
pp. 95-101
Author(s):  
Kosaku Maeda
2020 ◽  
Vol 10 (1) ◽  
pp. 95-102
Author(s):  
Nikolai V. Krivosheenko ◽  
Alexey V. Gramzin ◽  
Pavel M. Pavlushin ◽  
Yana L. Manakova ◽  
Larisa M. Shpak ◽  
...  

Introduction. The biggest difficulties of pulmonary sequestration treatment appear when they are combined with other congenital malformations. Materials and methods. This article describes a rare case of combination of infradiaphragmatic extralobar sequestration of the lung and duplication cyst of the gaster. The antenatal ultrasound investigation at 21 week of gestation visualized a retroperitoneal mass that had a cystic-solid structure and a vessel that departed directly from the aorta. CT-scan that was performed after the birth, confirmed an existence of infradiaphragmatic cystic mass that had a vessel that departed directly from the aorta. We couldnt exclude the neoplastic process because of structure and topography of mass. Tumor markers were without pathology. Surgical treatment was performed: laparotomy and removal of the cyst and extrapulmonary sequestration. The histological investigation confirmed a pulmonary sequestrum and duplication cyst of the gaster. Conclusion. A nowadays method of visualization allows to find congenital malformation in earliest stages of gestation. The tradition surgical treatment and also minimal invasive surgical treatment are the main option of cure such congenital malformations. Also literature review of rare clinical forms of pulmonary sequestration presented in this article.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Noboru Oyachi ◽  
Fuminori Numano ◽  
Keiichi Koizumi ◽  
Tamao Shinohara ◽  
Hirochika Matsubara

Abstract Background Several reports have documented that the pulmonary sequestration is in communication with the gastrointestinal tract and the concept of bronchopulmonary foregut malformation (BPFM) has become more widespread. However, there are few reports of the sequestration associated with the pancreas derived from the foregut. We describe the history and pathophysiology of BPFM including pancreatic tissue in a male infant with respiratory distress. Case presentation A male patient was born at 38 weeks of gestation and weighed 2752 g at birth. He developed pneumonia and was hospitalized at 3 months of age. Chest radiographs and CT scans led to the diagnosis of a lung abscess in the left lower intralobar pulmonary sequestration with aberrant arteries from the abdominal cavity. At 4 months of age, when the abscess had resolved, left lower lobectomy and the resection of the intralobar sequestration were performed. The pulmonary sequestration was conjoined with the esophagus. A fistula was found between the lower esophageal wall and the pulmonary sequestration. An additional small segment of the esophageal wall was excised. Histologically, the mediastinal surface of the sequestration tissue contained pancreatic tissue. Furthermore, esophageal and gastric tissue, cartilage tissue, and ciliated epithelium were confirmed. A definitive diagnosis of BPFM was made. Conclusions We postulated the rare case of a communicating BPFM with intrapulmonary sequestration on one end and the esophagus on the other forming a mass lesion, which included ectopic pancreatic tissue in a male infant.


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.


2013 ◽  
Vol 2013 ◽  
pp. 1-3
Author(s):  
R. L. McDermott ◽  
D. O. Kavanagh ◽  
W. Bartosik ◽  
C. Quinn ◽  
P. R. O'Connell

We report a case of a lady who presented with epigastric discomfort. Physical examination revealed a large left upper quadrant mass filling the left upper quadrant. Following extensive preoperative evaluation, she underwent resection of this centimeter mass withen blocexcision of a portion of the left hemidiaphragm. She made an uneventful postoperative recovery. Histopathology revealed a bronchopulmonary foregut malformation with pulmonary sequestration. This developmental anomaly of the foregut typically occurs in the thoracic cavity; however, it can occur below the diaphragm. Herein we report a case and a detailed review of the embryology, clinical features, and management of these extremely rare clinical entities.


2019 ◽  
Vol 26 (4) ◽  
pp. 223-228
Author(s):  
Su Kyung Kim ◽  
Jin Wha Choi ◽  
Hong Kwan Kim ◽  
Se In Sung ◽  
Yun Sil Chang ◽  
...  

2003 ◽  
Vol 53 (5) ◽  
pp. 313-316 ◽  
Author(s):  
Jun Matsubayashi ◽  
Tsuyoshi Ishida ◽  
Takashi Ozawa ◽  
Tatsuya Aoki ◽  
Yasuhisa Koyanagi ◽  
...  

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