Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 3 de 3
Filter
Add filters








Year range
1.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 1057-1059, 1999.
Article in Korean | WPRIM | ID: wpr-60015

ABSTRACT

Lymphangioleiomyomatosis(LAM) is defined as an abnormal proliferation of smooth muscles in the lung tissue throughout lymphatics, vascular and bronchial structure. A 52-year-old postmenopausal woman was admitted to our hospital for recurrent pneumothorax. She was treated for medroxyprogesterone by LAM 1 month ago. We performed operation of pulmonary partial resection and pleurodesis. The patient is receiving continuous medroxyprogesterone and Leuplin administration, and currently, 6 months after the operation, is still showing good results.


Subject(s)
Female , Humans , Middle Aged , Lung , Lung Neoplasms , Lymphangioleiomyomatosis , Lymphangioma , Medroxyprogesterone , Muscle, Smooth , Pleurodesis , Pneumothorax
2.
The Korean Journal of Thoracic and Cardiovascular Surgery ; : 432-435, 1998.
Article in Korean | WPRIM | ID: wpr-155288

ABSTRACT

Idiopathic cricopharyngeal achalasia is a rare condition that produces oropharyngeal dysphagia. It is caused by spasm of the cricopharyngeus and inability to relax with swallowing. A prominent muscle bar at the upper esophageal sphincter is a typical finding of the esophagogram. Cricopharyngeal myotomy is the treatment of choice. We report a case of cricopharyngeal myotomy for 61-year-old female patient.


Subject(s)
Female , Humans , Middle Aged , Deglutition , Deglutition Disorders , Esophageal Achalasia , Esophageal Sphincter, Upper , Pharyngeal Muscles , Spasm
3.
Journal of Korean Medical Science ; : 83-85, 1991.
Article in English | WPRIM | ID: wpr-169602

ABSTRACT

Pulmonary lymphangioleiomyomatosis has been observed almost exclusively in women, usually in their reproductive years. Exacerbations with pregnancy and after hormonal manipulation have been documented, and it has been suggested that its pathogenesis is due to the influence of hormonal(estrogenic) stimulus. The clinical, roentgenographic, and histopathologic features of this case of pulmonary lymphangioleiomyomatosis in a 22-year-old male are all characteristic of those described in prior reports, except for the patient's sex. With the following case of pulmonary lymphangioleiomyomatosis in a male, we suggest the possibility of the existence of an additional pathogenetic mechanism.


Subject(s)
Adult , Humans , Male , Emphysema/complications , Lung Neoplasms/complications , Lymphangiomyoma/complications , Lymphatic System/pathology , Muscle, Smooth/pathology , Thoracotomy/adverse effects , Tuberculosis, Pulmonary/complications
SELECTION OF CITATIONS
SEARCH DETAIL