|
|
||||||||
Ann Thorac Surg 2001;71:1704-1706
© 2001 The Society of Thoracic Surgeons
a Papworth Hospital NHS Trust, Cambridge, England, United Kingdom
Accepted for publication June 6, 2000.
* Address reprint requests to Dr Birdi, Department of Cardiothoracic Surgery, Papworth Hospital, Papworth Everard, Cambridge CB3 8RE, England (Email: inderuk{at}hotmail.com).
| Abstract |
|---|
|
|
|---|
| Introduction |
|---|
|
|
|---|
A 59-year-old man underwent surgery for squamous cell carcinoma involving the right lower lobe bronchus on October 13, 1985. Pneumonectomy was required because the tumor involved the right main bronchus. Initial recovery was uncomplicated.
He returned 8 months postoperatively with minimal stridor. Chest radiography showed some deviation of the mediastinum to the right. Rigid bronchoscopy performed at this stage was unremarkable.
The patient did not attend his routine outpatient appointments until he was re-referred 6 years later with progressive stridor, dyspnea on exertion, and repeated chest infections. He had chosen to neglect his symptoms until this time. A chest radiograph at this time demonstrated gross deviation of the mediastinum to the right, with hyperexpansion of the left lung. Computed tomography (Fig 1) showed rotation of the heart into the right posterior thorax. The trachea was very tortuous as it crossed the midline, and the left main bronchus was distorted in its course across the vertebral column. The left lung was herniating across the midline, virtually filling the entire chest. At bronchoscopy, the left main bronchus was slit-like over the vertebral column and would not admit a flexible scope. There were no malacic features. It was felt that simple endoscopic stent insertion would not be successful, and surgical correction of the deviation followed by plombage was therefore performed on December 14, 1992.
|
The patient experienced considerable improvement in his stridor immediately postoperatively, and at 6-week follow-up he was symptom free. Computed tomography performed 6 years after plombage demonstrated complete integrity of the saline implants (Fig 2). The patient was participating in circuit training exercise at that time.
|
| Comment |
|---|
|
|
|---|
The use of an expandable silicone prosthesis, as used in plastic surgery, was first described by Rasch and colleagues [5] in a 5-month old child who had previously undergone right pneumonectomy for total pulmonary sequestration. The ability to gradually increase the volume of the prosthesis is useful in children to accommodate changes in intrathoracic size as a result of growth. In adults, this has also been of value in graduating mediastinal correction by progressive injection of saline through a subcutaneous port [2]. Conversely, there are reports of leakage of the prosthesis caused by overinflation and injury [5, 6] and therefore the shape and size of the prosthesis must be determined carefully.
Some workers have combined mediastinal correction and cardiopexy, with the implantation of prosthetic breast [1, 7]. We believe that this method has a number of advantages over other plombage techniques. After correction of mediastinal position, a varying number of saline breast implants can be inserted into the chest. The ability of these implants to alter their shape in relation to the inside of the chest wall and also to one another make them advantageous to other plombage devices. In addition, the relatively low pressure of the contents of these prostheses as well as the durability of their walls may make them less likely to rupture. In our patient, CT scanning was repeated 6 years after saline prosthesis plombage. This confirmed the integrity of the implants.
Our patient showed no clinically important evidence of bronchomalacia despite the fact that he was clearly symptomatic over the 7-year period between his right pneumonectomy and surgical plombage. In a series of 11 patients with this syndrome, Grillo and colleagues [1] observed bronchomalacia only in patients in whom the bronchus was interposed between the pulmonary artery and aorta and not in those where the bronchus lay between the pulmonary artery and the spine as was the situation in our case.
The development of stridor after pneumonectomy needs to be carefully assessed by bronchoscopy and CT in order to exclude the early manifestations of postpneumonectomy syndrome. Mediastinal correction and cardiopexy combined with plombage of the pneumonectomy space with saline breast prostheses can be an effective long term treatment option. The occurrence of bronchomalacia is not invariably present in those with a protracted postpneumonectomy history suggestive of this syndrome and may be more closely related to the anatomical position of the bronchus in relation to neighboring vascular structures.
| References |
|---|
|
|
|---|
This article has been cited by other articles:
![]() |
C. Soll, D. Hahnloser, T. Frauenfelder, E. W. Russi, W. Weder, and P. B. Kestenholz The postpneumonectomy syndrome: clinical presentation and treatment Eur J Cardiothorac Surg, February 1, 2009; 35(2): 319 - 324. [Abstract] [Full Text] [PDF] |
||||
![]() |
G. Rakovich, J. Bussieres, and E. Frechette Postpneumonectomy syndrome MMCTS, January 1, 2009; 2009(0831): mmcts.2008.003475 - mmcts.2008.003475. [Abstract] [Full Text] [PDF] |
||||
![]() |
C. Gebitekin and A. S. Bayram Post-Pneumonectomy Syndrome in an Adult Presenting with Positional Syncope Asian Cardiovascular and Thoracic Annals, February 1, 2006; 14(1): e12 - e13. [Abstract] [Full Text] [PDF] |
||||
| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |