| Literature DB >> 667807 |
H Kreisman, Y Robitaille, G P Dionne, M J Palayew.
Abstract
A 48-year-old woman presented with the classical clinicopathological features of the lymphangiomyomatosis syndrome. After a three year stable period, there was the onset of a rapidly progressive downhill course unresponsive to dietary, bronchodilator and corticosteroid therapy. Pathological findings were characterized by widespread pulmonary, thoracic duct and lymph node involvement. There was a mediastinal lymphangiomyoma growing within the distal thoracic duct, and a similar lesion within the left kidney which could clinically mimic an angiomyolipoma. Comments are also made on the finding of a parathyroid adenoma. The physiopathology and possible resemblance to "formes frustes" of tuberous sclerosis are discussed.Entities:
Mesh:
Year: 1978 PMID: 667807 DOI: 10.1002/1097-0142(197807)42:1<364::aid-cncr2820420155>3.0.co;2-m
Source DB: PubMed Journal: Cancer ISSN: 0008-543X Impact factor: 6.860