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Showing papers by "Peter Goldstraw published in 2001"


Journal ArticleDOI
TL;DR: A patient who went on to develop PPB in the right lung despite having had resections for bilateral congenital pulmonary cysts 23 months earlier is reported, raising questions of the effectiveness of prophylactic resection of congenital lung cysts on this basis.

86 citations


Journal ArticleDOI
TL;DR: Surgical treatment achieved a reasonable survival in a small subgroup of patients where radiotherapy had failed or was deemed inappropriate because of the size or location of the tumor.

21 citations


Journal ArticleDOI
TL;DR: A case in which there was also malignant transformation in the cyst wall, manifested by invasive adenocarcinoma and widespread high-grade glandular dysplasia is presented.

13 citations


Journal ArticleDOI
TL;DR: Histological examination of the two lesions resected showed them to be a foregut cyst and a benign mesothelial cyst, and it is hypothesized that these cysts may have a common embryonic origin.
Abstract: A 14-year-old male was found to have a mediastinal mass on chest radiograph. Chest computed tomography scans showed a cystic lesion behind the left main bronchus. Magnetic resonance imaging revealed additional cystic lesions in the left chest and root of the neck. He underwent excision of mediastinal mass and a pleural cyst. The neck lesion was presumed to be a cystic hygroma. Histological examination of the two lesions resected showed them to be a foregut cyst and a benign mesothelial cyst. We know of no other report of concurrent multicystic lesions in the chest and neck and hypothesize that these cysts may have a common embryonic origin.

12 citations


Journal ArticleDOI
01 Jul 2001-Thorax
TL;DR: The case history is presented of a patient in whom an intramural tracheal neurofibroma developed, causing severe airway stenosis, and Clinicians should be aware of this rare complication of Neurofibromatosis.
Abstract: The case history is presented of a patient in whom an intramural tracheal neurofibroma developed, causing severe airway stenosis. The patient was treated with multiple stents over a period of 5 years because of progression of the disease and associated airflow limitation. Clinicians should be aware of this rare complication of neurofibromatosis.

9 citations