Chylothorax in Lymphangioleiomyomatosis

• Published in: Chest Vol. 123; no. 2; pp. 623 - 627
• Main Authors: Ryu, Jay H., Doerr, Clint H., Fisher, Susan D., Olson, Eric J., Sahn, Steven A.
• Format: Journal Article
• Language: English
• Published: Northbrook, IL Elsevier Inc 01.02.2003; American College of Chest Physicians
• Subjects: Adult; Ascites; Biological and medical sciences; Biopsy; chylothorax; Chylothorax - diagnosis; Chylothorax - surgery; Comorbidity; Dyspnea; Female; Follow-Up Studies; Humans; Lung Diseases - diagnosis; Lung Diseases - surgery; lymphangioleiomyomatosis; Lymphangioleiomyomatosis - diagnosis; Lymphangioleiomyomatosis - surgery; Medical records; Medical sciences; Middle Aged; Ostomy; Patients; Pleura - surgery; Pleural effusion; Pneumology; Respiratory system : syndromes and miscellaneous diseases; Retrospective Studies; Thoracentesis; Thoracic Duct - surgery; Thoracostomy; Thoracotomy; Tomography, X-Ray Computed; tuberous sclerosis complex; tuberous sclerosis complex; TSC; chylothorax; LAM; HRCT; pleural effusion; lymphangioleiomyomatosis; Diffuse; Human; Lung disease; Lymphangiomatosis; Effusion; Respiratory disease; Leiomyomata; Lung; Clinical form; Cardiovascular disease; Bronchopulmonary; Lymphatic vessel disease; Bronchus disease; Pleural disease; Benign neoplasm; Chylothorax
• ISSN: 0012-3692; 1931-3543
• DOI: 10.1378/chest.123.2.623

Pulmonary lymphangioleiomyomatosis (LAM) is a rare, serious disorder characterized by proliferation of abnormal smooth-muscle cells and affects almost exclusively women of childbearing age. Optimal management of chylothorax, a well-recognized complication of LAM, in these patients has not been defined. This study was performed to characterize the clinical course and identify appropriate management options for chylothorax occurring in patients with LAM. Identification and retrospective review of available medical records on patients with LAM and chylothorax. Tertiary-referral medical center. All patients with LAM seen at Mayo Clinic, Rochester, MN, from January 1, 1976, to December 31, 2000. None. Eight of 79 patients (10.1%) with LAM had chylothorax. All were women aged 33 to 51 years, and four patients had underlying tuberous sclerosis complex. These eight women represented 3.5% of the 229 patients with chylothorax seen over this 25-year period at Mayo Clinic Rochester. Six patients had unilateral pleural effusion and two patients had bilateral effusions at initial presentation. The size of the chylothorax varied and was not necessarily progressive. Management of chylothorax ranged from thoracentesis only to thoracotomy with thoracic duct ligation and parietal pleurectomy. When needed, pleurodesis by instillation of sclerosing agents or parietal pleurectomy appeared to be effective in controlling chylothorax. Chylothorax occurring in patients with LAM has a variable clinical course. Although pleurodesis with or without thoracic duct ligation appears to be effective in controlling intractable chylothorax, less invasive treatments such as thoracentesis or observation may suffice in some cases. Management of chylothorax in patients with LAM should be individualized depending on the size and clinical effects of the chylous pleural effusion, as well as comorbid factors and local expertise.