Abstract:
:Lymphangioleiomyomatosis (LAM) is a progressive disorder of unknown etiology that predominantly affects the lungs, and the resulting respiratory failure can be fatal. Extrapulmonary LAM is a rare disease that often occurs concurrently with pulmonary LAM. Usually, extrapulmonary LAM presents as a localized, well-circumscribed mass. Due to the rare occurrence of extrapulmonary LAM and its atypical location, extrapulmonary LAM is often difficult to diagnose prior to surgery. The present study describes the clinicopathological features of primary liver LAM in a 26-year-old woman. To the best of our knowledge, the present study presents the first case of a primary solitary extrapulmonary form of LAM in the liver.
journal_name
Exp Ther Medjournal_title
Experimental and therapeutic medicineauthors
Fu W,Li Y,Li H,Yang P,Xing Xdoi
10.3892/etm.2016.3502subject
Has Abstractpub_date
2016-09-01 00:00:00pages
1499-1502issue
3eissn
1792-0981issn
1792-1015pii
ETM-0-0-3502journal_volume
12pub_type
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