[Birt-Hogg-Dubé Syndrome Diagnosed with Surgery;Report of Three Cases].

Birt-Hogg-Dubé (BHD) syndrome is an autosomal and predominantly inherited disorder. We report 3 cases of BHD syndrome. Case 1:A 24-year-old man was admitted to our hospital due to left-sided spontaneous pneumothorax.

Pulmonary Artery Pseudoaneurysm Secondary to Lung Inf lammation.

Pulmonary artery aneurysms (PAA) and pseudoaneurysms (PAP) are caused by infections, vasculitis, trauma, pulmonary hypertension, congenital heart disease, and connective tissue disease. Most cases of such aneurysm occur in the trunk or major branches of the pulmonary artery, while the peripheral type is less common. The treatment modalities are medical therapy, surgery, and percutaneous catheter embolization.

Mycotic pseudoaneurysm of a pulmonary artery branch caused by Cladosporium.

We report the case of a 53-year-old male with a history of acute myelogenous leukemia, who suffered the rupturing of a right-sided pulmonary artery pseudoaneurysm combined with pneumonia. He underwent a right-sided lower lobectomy. The resected lung tissue demonstrated a mycotic pseudoaneurysm of a pulmonary artery branch together with a filamentous fungal infection.

Lobar emphysema with pneumothorax in an adult: report of a case.

A 31-year-old woman was transferred to our hospital for treatment of a right pneumothorax. She had presented initially with moderate dyspnea and coughing at a local clinic, where a chest radiograph showed a collapsed right lung. Chest computed tomography showed overinflation of the middle lobe and a large bulla.

Treatment strategies for chronic expanding hematomas of the thorax.

Purpose: To investigate retrospectively the treatment strategies for chronic expanding hematoma (CEH) of the thorax.

Methods: We reviewed the medical records of six patients treated for CEH of the thorax at our institution between October 1996 and October 2006.

Results: All of the patients had a history of thoracic surgery or tuberculosis with a latent period of 12-55 years before onset.

Surgical treatment of catamenial pneumothorax.

Objective: To discuss the aetiology and determine the optimal surgical treatment of catamenial pneumothorax.

Methods: Between January 1980 and December 2007, 17 patients with catamenial pneumothorax were treated at our institution. Regarding the surgical approach, thoracotomy was performed until 1991, and thoracoscopic surgery was performed from 1992 onward.

Preventing recurrence of spontaneous pneumothorax after thoracoscopic surgery: a review of recent results.

Spontaneous pneumothorax (SP) is now commonly treated with thoracoscopic surgery, which is associated with less pain and a shorter hospital stay than thoracotomy; however, in its initial stages, thoracoscopic stapled bullectomy resulted in an unexpectedly high incidence of postoperative SP recurrence. Thus, new thoracoscopic procedures, designed to be performed in addition to stapled bullectomy, were developed, which resulted in a gradual decline in the postoperative recurrence rate. We review the recent literature on SP recurrence after thoracoscopic surgery with these other surgical procedures.