Pulmonary Rhabdomyosarcoma Associated with Check-Valve Mechanism

2017 ◽  
Vol 196 (3) ◽  
pp. e7-e9
Author(s):  
Udit Chaddha ◽  
Jeffrey A. Hagen ◽  
Bassam Yaghmour
Keyword(s):  
2017 ◽  
Vol 55 (1) ◽  
pp. 63-68 ◽  
Author(s):  
Aya Hirata ◽  
Takeshi Saraya ◽  
Nobuaki Arai ◽  
Shin Karita ◽  
Riken Kawachi ◽  
...  

CHEST Journal ◽  
1991 ◽  
Vol 100 (3) ◽  
pp. 853-855 ◽  
Author(s):  
Hironobu Minami ◽  
Shuzo Sakai ◽  
Atsushi Watanabe ◽  
Kaoru Shimokata

The Lancet ◽  
1958 ◽  
Vol 271 (7013) ◽  
pp. 222
Author(s):  
G.C.R. Morris ◽  
J.G. Widdicombe
Keyword(s):  

PEDIATRICS ◽  
1959 ◽  
Vol 24 (6) ◽  
pp. 1050-1064
Author(s):  
Edwin J. Liebner

Normally, the bronchi dilate rapidly in inspiration and contract slowly in expiration, thus effecting a form of check-valve mechanism. Intra-and extra-bronchial occlusion, pulmonary infection, developmental bronchopulmonary malformations and pleural communications are pathologic processes which can disturb the check-valve mechanism and produce increased aeration. [See Figure in Source Pdf.] The main bronchus and artery may be obstructed separately, or as a unit. Angiocardiograms should be analyzed for abnormal patterns, especially obstruction or atresia. A lack of vascular markings in the lungs can suggest pseudo-increased aeration. On a regional basis, roentgenographic study of the vascular and air patterns can lead to recognition of certain entities. An angiogram in congenital lobar emphysema contrasts the vascular pattern in the involved and the remaining normal and unaffected lobes with pneumatocele, cystic disease, and atelectasis. Reasons for support of the deficient-cartilage theory as a cause of lobar emphysema are cited, with emphasis on the localization of the emphysema to the anterior or upper lobes. Bronchiolitis can give total compensatory emphysema, and the reasons given will help to understand the roentgenographic findings. Regional compensatory emphysema of the remaining lung, after total or partial collapse of a lobe by intrinsic or extrinsic factors, is illustrated. Basal pneumothorax is indicated to be a significant postoperative complication. Although at times great similarity may exist in the appearance of plain films in conditions producing increased aeration of infants' lungs, it is hoped that this review will stimulate deeper analyses and wider recognition of the fundamentals.


The Lancet ◽  
1958 ◽  
Vol 271 (7015) ◽  
pp. 317-318 ◽  
Author(s):  
W.A. Lister
Keyword(s):  

2012 ◽  
Vol 155 (2) ◽  
pp. 309-313 ◽  
Author(s):  
Shunji Asamoto ◽  
Yasuyuki Fukui ◽  
Makoto Nishiyama ◽  
Masayuki Ishikawa ◽  
Nobuyuki Fujita ◽  
...  

2020 ◽  
Vol 3 (3) ◽  
pp. 73-78
Author(s):  
Gouthami Chennu ◽  
Paulina Przydzial ◽  
Yee Tchao ◽  
Anthony Isedeh ◽  
Nikhil Madan

Pulmonary pneumatocele is a cystic, air-filled lesion in the lung parenchyma. It results from underlying inflammation or bronchial injury. It is seen in several lung pathologies including bacterial pneumonia, positive-pressure ventilation, chest trauma, chemical pneumonitis, and is most often seen in infants and children. On imaging, pneumatoceles appear as rounded, thin-walled, air-filled spaces in the lung parenchyma. The exact mechanism for forming pneumatoceles is not fully understood but thought to be due to a check-valve mechanism due to obstruction by inflammation causing air trapping in the damaged lung. These lesions are asymptomatic and transient in most patients and disappear by about 6 weeks. They usually do not require any specific treatment or intervention. Surgical intervention is only necessary when pneumatoceles cause cardiopulmonary compromise or rupture into the pleural space. We describe a case of a young adult who developed a pneumatocele after developing acute respiratory distress syndrome from community-acquired pneumonia treated with positive-pressure ventilation. He was managed conservatively with complete resolution of symptoms.


The Lancet ◽  
1958 ◽  
Vol 271 (7011) ◽  
pp. 66-70 ◽  
Author(s):  
W.A. Lister
Keyword(s):  

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