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Hum Pathol ; 28(12): 1420-3, 1997 Dec.
Article in English | MEDLINE | ID: mdl-9416700

ABSTRACT

Lymphangioleiomyomatosis (LAM) is a rare disease which afflicts young women of childbearing age. Recently, it has been listed as an indication for lung transplantation. We describe a case of recurrent LAM in a 31-year-old woman occurring in the allograft of a male donor after single lung transplantation. Nonisotopic in situ hybridization shows that the smooth muscle cell proliferation is of donor origin.


Subject(s)
Lung Transplantation/pathology , Lymphangioleiomyomatosis/pathology , Lymphangioleiomyomatosis/surgery , Postoperative Complications/pathology , Adult , Cell Division , Female , Humans , Muscle, Smooth/pathology , Pulmonary Alveoli/pathology , Recurrence
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