Tracheal Bronchus Associated With Unilateral Absence of Pulmonary Artery and Recurrent Pneumonia

2016 ◽  
Vol 7 (2) ◽  
Author(s):  
Iraj Sedighi ◽  
Mehrnaz Olfat ◽  
Neda Pak ◽  
Maryam Nasr Esfahany
2020 ◽  
Vol 48 (10) ◽  
pp. 030006052096760
Author(s):  
Yuangui Zhang ◽  
Meiman Qin ◽  
Xiaoqian Wang ◽  
Quanzhang Yan

A tracheal bronchus is a rare congenital anomaly, suggesting abnormal bronchial development. The prevalence of tracheal bronchus in children who undergo bronchoscopy is estimated to be between 0.2% and 3%. When associated with recurrent infection, lobes of the lung must be removed to avoid further lung injury. In such cases, perioperative one-lung ventilation and airway management remain a huge challenge for anaesthesiologists. The case of this rare airway anatomic abnormality in a paediatric patient with two bronchial openings into the right upper lobe, and with a history of recurrent pneumonia, is reported. In addition to a normal opening, a distinct opening in the upper lobe of the right lung was observed, that originated directly from the trachea, superior to the carina. The entire right lung was deflated by left-lung ventilation using a single lumen tracheal tube, and the patient underwent right upper lobe resection. No anaesthesia complications were observed during recovery. In this case, timely identification of the tracheal bronchus and successful collapse of the right lung were key points in the anaesthesia management of this patient.


2017 ◽  
Vol 72 (1) ◽  
pp. 81-82
Author(s):  
Kai-Li Wang ◽  
Yun-Ching Fu ◽  
Sheng-Ching Chan ◽  
Ming-Chih Lin ◽  
Sheng-Ling Jan

2013 ◽  
Vol 19 (4) ◽  
pp. 302-304 ◽  
Author(s):  
Marlina Lovett ◽  
Daniel Entrikin ◽  
Ross Ungerleider ◽  
Yoshio Ootaki

2011 ◽  
Vol 18 (2) ◽  
pp. 84-86 ◽  
Author(s):  
Cecilia T Costiniuk ◽  
Nha Voduc ◽  
Carolina de Souza

BACKGROUND: Tracheal bronchus is a congenital malformation comprising an abnormal bronchus originating from the trachea or other bronchus. This malformation has been associated with recurrent pneumonia in children, but is rarely associated with infection in adults.Actinomycesspecies are rare causes of necrotizing pneumonias that often masquerade as malignancy, lung abscesses and tuberculosis.METHODS AND RESULTS: A case involving a 46-year-old man with a tracheal bronchus and chronic pneumonia syndrome is presented. Bronchialveolar lavage and transthoracic needle biopsy demonstrated the presence ofActinomyces meyeriandFusobacteriumspecies.CONCLUSIONS: The present article reports the first documented case of actinomycosis occurring in a patient with a tracheal bronchus.


Angiology ◽  
1989 ◽  
Vol 40 (9) ◽  
pp. 849-853
Author(s):  
Daniela Lax ◽  
Fouad Butto ◽  
Stanley A. Leonard ◽  
W. Steves Ring ◽  
Ann Dunnigan

2013 ◽  
Vol 63 (3) ◽  
pp. 173-176 ◽  
Author(s):  
Takuro Miyazaki ◽  
Naoya Yamasaki ◽  
Tomoshi Tsuchiya ◽  
Keitaro Matsumoto ◽  
Hideyuki Hayashi ◽  
...  

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