Pulmonary lymphangioleiomyomatosis--a case report.

Pol J Pathol

Department of Pathomorphology, Medical Academy, Lublin.

Published: December 1996

Lymphangioleiomyomatosis is a rare disease entity. A case of a 51-year-old man treated for respiratory insufficiency has been reported. Due to disseminated lesions in the pulmonary tissue the patient was assessed for the presence of sarcoidosis. Histopathological examination of the lung specimen obtained during videothoracoscopy revealed lesions of the lymphangioleiomyomatosis type.

Download full-text PDF

Source

Publication Analysis

Top Keywords

pulmonary lymphangioleiomyomatosis--a
4
lymphangioleiomyomatosis--a case
4
case report
4
report lymphangioleiomyomatosis
4
lymphangioleiomyomatosis rare
4
rare disease
4
disease entity
4
entity case
4
case 51-year-old
4
51-year-old man
4

Similar Publications

Pulmonary lymphangioleiomyomatosis--a case report.

J Cancer Res Ther

August 2015

Institute of Traditional Chinese Medicine Research, Tianjin State Key Laboratory of Modern Chinese Medicine, Tianjin University of Traditional Chinese Medicine, Tianjin 300193, China.

Pulmonary lymphangioleiomyomatosis (PLAM) is a rare disease, occurs in 16-68-year-old women, especially in women of childbearing age. High-resolution computed tomography would be useful for diagnosis of PLAM. Immunohistochemistry of smooth muscle actin (SMA) and HMB-45 smooth muscle cells was positive for smooth muscle cells.

View Article and Find Full Text PDF

Tuberous sclerosis complex (TSC) manifests predominantly as a neurocutaneous disorder. Lymphangioleiomyomatosis (LAM) is a rare pulmonary manifestation of TSC. Imaging evaluation plays an important role in the assessment of patients with tuberous sclerosis complex.

View Article and Find Full Text PDF

Pulmonary lymphangioleiomyomatosis--a silent killer?

J Assoc Physicians India

May 2012

Department of Medicine, Nilratan Sircar Medical College, 138, A J C Bose Road, Kolkata 700014.

Pulmonary lymphangioleiomyomatosis (LAM) is a rare disorder presenting with remarkable features like recurrent pneumothorax or chylothorax, usually in young women. We report a case of sporadic LAM who presented with nothing but recent onset exertional dyspnoea and it was this unobtrusive presentation that led to delay in diagnosis.

View Article and Find Full Text PDF

Lymphangioleiomyomatosis--a brief review and estimation of excess risk.

J Insur Med

March 2012

Samsung Life Service Co. 10th Fl. Samsung-Jeil Bldg, 702-2, Yeoksam-Dong, Gangnam-Gu, Seoul, Korea, 135-751.

Lymphangioleiomyomatosis (LAM) is a rare pulmonary disease in women of child-bearing age. It is multisystem disease and affects mainly the lungs. A recently published Korean medical article showed a sharp increase of LAM patients in Korea since 2004.

View Article and Find Full Text PDF

A 32-year-old woman was admitted with persistent dyspnea. Chest roentgenogram showed hyperinflation of the lungs, and diffuse reticular shadows in both lung fields. Chest CT showed diffuse cystic lesions and thickened vasculature.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!