Journal Information
Vol. 51. Issue 12.
Pages 655 (December 2015)
Vol. 51. Issue 12.
Pages 655 (December 2015)
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Pneumothorax and Congenital Diaphragmatic Hernia: An Unusual Combination
Neumotórax y hernia diafragmática congénita, una asociación infrecuente
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José Soro, Montserrat Blanco
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montseblancoramos@hotmail.com

Corresponding author.
, Eva García-Fontán
Servicio de Cirugía Torácica, Complejo Hospitalario Universitario de Vigo, Hospital Xeral-Cíes, Vigo, Pontevedra, España
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A 41-year-old woman with a history of spontaneous right pneumothorax, treated with thoracic drainage, was evaluated in our department for a relapse of the same condition. Chest X-ray revealed, in addition to pneumothorax, diaphragmatic lobulation (Fig. 1a, arrow). Video-assisted thoracoscopy revealed congenital diaphragmatic hernia (Fig. 1b), which was repaired with separate monofilament sutures. No other lesions were identified that could explain the origin of the pneumothorax (Fig. 1c). The patient was discharged on day 4 after surgery, with no complications.1

Fig. 1.

(a) Posterolateral chest X-ray showing complete right pneumothorax with no mediastinal shift. Diaphragmatic lobulation is also seen (arrow). (b) Right diaphragmatic herniation on video-assisted thoracoscopy, showing the hepatic dome. (c) Herniation closed by separate monofilament sutures.

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Reference
[1]
S. Sanna, M. Taurchini, M. Monteverde, V. Agnoletti, G.L. Casoni.
Catamenially recurring pneumothorax with partial liver herniation: a particular view.
Respiration, 82 (2011), pp. 476-477

Please cite this article as: Soro J, Blanco M, García-Fontán E. Neumotórax y hernia diafragmática congénita, una asociación infrecuente. Arch Bronconeumol. 2015;51:655.

Copyright © 2015. SEPAR
Archivos de Bronconeumología
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