scholarly journals Surgical Management of Bronchial Stump Complication in Cadaveric Lobar Lung Transplantation

2021 ◽  
Vol 40 (4) ◽  
pp. S505
Author(s):  
J.P. Ehrsam ◽  
O. Lauk ◽  
S. Hillinger ◽  
D. Schneiter ◽  
I. Opitz ◽  
...  
2020 ◽  
Vol 52 (2) ◽  
pp. 596-598
Author(s):  
Anna Muñoz Fos ◽  
Francisco Cerezo Madueño ◽  
Javier Cosano ◽  
Javier Redel ◽  
Javier González García ◽  
...  

1990 ◽  
Vol 49 (2) ◽  
pp. 333-340 ◽  
Author(s):  
B. Reichart ◽  
S. Vosloo ◽  
J. Holl

Surgery Today ◽  
2021 ◽  
Author(s):  
Eleonora Faccioli ◽  
Andrea Dell’Amore ◽  
Pia Ferrigno ◽  
Marco Schiavon ◽  
Marco Mammana ◽  
...  

Abstract Purpose Bronchial stenoses are challenging complications after lung transplantation and are associated with high rates of morbidity and mortality. We report a series of patients who underwent bronchoplasty or sleeve resection for bronchial stenoses that did not resolve with endoscopic treatment after lung transplantation. Methods Between 1995 and 2020, 497 patients underwent lung transplantation at our Institution. 35 patients (7.0%) experienced bronchial stenoses with a median time from transplantation of 3 months. Endoscopic management was effective in 28 cases (5.6%) while 1 patient required re-transplantation. Six patients (1.2%) underwent bronchoplasty or sleeve resection. Results The procedures of the six patients who underwent bronchoplasty or sleeve resection were as follows: lower sleeve bilobectomy (n = 3), wedge bronchoplasty of the bronchus intermedius (n = 1), isolated sleeve resection of the bronchus intermedius (n = 1), and isolated sleeve resection of the bronchus intermedius (n = 1), associated with a middle lobectomy. All patients were discharged after a median time of 11 days. At a median of 12 months from surgery, two patients remain alive with a preserved pulmonary function. Four patients died after a median time of 56 months from bronchoplasty of causes that were not related to surgery. Conclusions Bronchial reconstructions are challenging procedures that can be performed in highly specialized centers. Despite this, they can be considered a good strategy to obtain a definitive resolution of stenosis after lung transplantation.


2018 ◽  
Vol 156 (1) ◽  
pp. 451-460 ◽  
Author(s):  
Hidenao Kayawake ◽  
Toyofumi F. Chen-Yoshikawa ◽  
Akihiro Aoyama ◽  
Hideki Motoyama ◽  
Masatsugu Hamaji ◽  
...  

2020 ◽  
pp. 1-3
Author(s):  
Laurent Dercle ◽  
Aiping Chen ◽  
Fatima-Zohra Mokrane ◽  
Laurent Dercle

Pulmonary alveolar microlithiasis (PAM) is a rare lung disease with poor prognosis. The only effective treatment to date, is lung transplantation in the severest cases. However, the etiology of PAM has been recently deciphered, and the treatment paradigm is shifting. We report a case of PAM and propose an optimized imaging-guided management based on the current state of the art.


1990 ◽  
Vol 49 (1) ◽  
pp. 147-149 ◽  
Author(s):  
A.J.B. Kirk ◽  
I.D. Conacher ◽  
P.A. Corris ◽  
T. Ashcroft ◽  
J.H. Dark

2019 ◽  
Vol 4 (5) ◽  
pp. 857-869
Author(s):  
Oksana A. Jackson ◽  
Alison E. Kaye

Purpose The purpose of this tutorial was to describe the surgical management of palate-related abnormalities associated with 22q11.2 deletion syndrome. Craniofacial differences in 22q11.2 deletion syndrome may include overt or occult clefting of the palate and/or lip along with oropharyngeal variances that may lead to velopharyngeal dysfunction. This chapter will describe these circumstances, including incidence, diagnosis, and indications for surgical intervention. Speech assessment and imaging of the velopharyngeal system will be discussed as it relates to preoperative evaluation and surgical decision making. Important for patients with 22q11.2 deletion syndrome is appropriate preoperative screening to assess for internal carotid artery positioning, cervical spine abnormalities, and obstructive sleep apnea. Timing of surgery as well as different techniques, common complications, and outcomes will also be discussed. Conclusion Management of velopharyngeal dysfunction in patients with 22q11.2 deletion syndrome is challenging and requires thoughtful preoperative assessment and planning as well as a careful surgical technique.


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