CT findings of anomalous systemic artery to the left lower lobe: Comparison with pulmonary sequestration in the left lower lobe

2014 ◽  
Vol 69 (12) ◽  
pp. e485-e490 ◽  
Author(s):  
J. Qin ◽  
S.-H. Huang ◽  
R.-H. Yan ◽  
Y.-X. Dong ◽  
H. Shan
2015 ◽  
Vol 56 (9) ◽  
pp. 1100-1104 ◽  
Author(s):  
Jie Qin ◽  
Xiao-li Wang ◽  
Ming-jun Bai ◽  
Shao-hong Huang ◽  
Xiu-zhen Chen ◽  
...  

2016 ◽  
Vol 88 (5) ◽  
pp. 510-510
Author(s):  
Sameer Thakur ◽  
Siew Simg Christine Goh ◽  
Rajiv Sharma ◽  
Ashutosh Hardikar

2017 ◽  
Vol 2 (1) ◽  

Intralobar sequestration accounts for 75% of pulmonary sequestrations. It is characterized by the presence of nonfunctional parenchymal lung tissue, receiving systemic arterial blood supply. We conducted a retrospective medical records review of all patients evaluated and treated in our pulmonary department of military hospital of Tunisia with diagnosis of PS from January 2007 through December 2015. Among them, we report 5 cases of intralobar pulmonary sequestrations operated. There are three women and two men; the mean age is 27.6 years. The sequestration was intralobar in all cases. Clinical presentations were chest pain and productive cough in three cases. Chest X-ray showed left basal opacity in three cases, bilateral basal reticulonodular opacities in one case and round hydric opacity in the right lower lobe in one other case. Computed tomography was performed and revealed an aberrant systemic artery born from the lateral side of aorta supplying a left lower lobe sequestration in four cases and a right lower lobe mass in only one case. The confirmation was operative in all cases and histologic only in three cases. All patients were treated by lobectomy. Only one case presented with a pulmonary sequestration combined with tuberculosis and he was treated firstly by antituberculous chemotherapy. The results were excellent with a favorable clinical course and the mortality was nil.


2018 ◽  
Vol 1 (3) ◽  
pp. 104-106
Author(s):  
Wahid Lana ◽  
◽  
Icard Bradley ◽  
Pelleg Tomer ◽  
Ie Susanti ◽  
...  

Pulmonary sequestration is a rare congenital abnormality especially in the adult population. It can commonly present as a cause for recurrent pneumonia or be found incidentally as an adult on imaging. We present a case of left lower lobe celiac trunk pulmonary sequestration in the setting of recurrent pneumonia to include histoplasmosis.


2021 ◽  
Vol 9 (27) ◽  
pp. 8192-8198
Author(s):  
Yi-Yuan Zhang ◽  
Xiao-Ying Gu ◽  
Jia-Lin Li ◽  
Zhao Liu ◽  
Guo-Yue Lv

2006 ◽  
Vol 24 (10) ◽  
pp. 687-689 ◽  
Author(s):  
Tamaki Matsunami ◽  
Kazuhiro Suzuki ◽  
Koremochi Takata ◽  
Yoshihisa Kurosaki

2008 ◽  
Vol 65 (1) ◽  
pp. 33-39
Author(s):  
Vlado Cvijanovic ◽  
Vojkan Stanic ◽  
Aleksandar Ristanovic ◽  
Bojan Gulic ◽  
Davor Stamenovic ◽  
...  

Background/Aim. Pulmonary sequestration is a congenital malformation which consists of a functional part of the lung, separated of the normal airway, and vascularisated with anomal systemic artery instead of pulmonary artery. There are two kinds of sequestration. Intralobar is surrounded with normal lung and its pleura, and extralobar which has extrapulmonary position and pleura of its own. This anomaly is very rare and appears in 1.1?1.8% of all congenital lung malformations. The illness is revealed either in early childhood with other life-threatening anomalies or in adulthood and middle age when secondary infection arises. The aim of this paper was to show our own experience in surgical treatment of pulmonary sequestration and to emphasize sequestration as a real differential-diagnostic possibility with patients with recidive bronchopneumonias. Methods. We retrospectively analyzed medical records for the period from 1967?2007 and found 15 patients with pulmonary sequestration at the average age of 30 years. We pointed out the well known problems with identification of this anomaly, preoperative diagnostic procedures and surgical possibilities of treatment. Results. There were 13 patients with intralobar and two patients with extralobar sequestration. By the use of preoperative angiography, seven patients were found to have intralobar pulmonary sequestration. All intralobar sequestrations were clinically manifested, the most often with recidive bronchopneumonia. Six patients had no preoperative diagnosis of lung sequestration. The most common locality of intralobar sequestration was the left lower lobe (eight patients). We performed nine lobectomies, three sequestrectomies, two segmentectomies and one pneumonectomy. Both extralobar sequestrations were diagnosed intraoperatively. Conclusion. Pulmonary sequestration is a rare malformation. Diagnosis is established by angiography. Treatment is exclusively surgical. In the last three years we have had one patient per year. This experience obliges to consider pulmonary sequestration as a real differential- diagnostic possibility in patients with localized repeated bronchopneumonias.


2016 ◽  
Vol 73 (11) ◽  
pp. 1060-1063
Author(s):  
Tatjana Adzic-Vukicevic ◽  
Dragan Radovanovic ◽  
Bojana Acimovic ◽  
Marko Popovic

Introduction. Pulmonary sequestration is a rare congenital anomaly and most intralobar sequestrations were located in lower lobes. Case report. We reported an unusual 28-yearold female patient with intralobar pulmonary sequestration on the left lower lobe, successfully treated with lobectomy. Computed tomography (CT) of the chest with intravenous contrast revealed multiple clustered cystic lesions in the left lower lobe with aberrant artery from descedenting aorta. Additional aortography showed an aberrant artery (3 mm in diameter) arising from the abdominal aorta and flowing into the lesion. Conclusion. Standard therapy regimen for pulmonary sequestration includes surgery. CT scan of thorax with intravenous contrast and aortography represent the gold standard for its diagnosis. Tumor-like shadows seen on the chest radiography or CT scans should not be always suspected on malignant lesions.


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