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Bilateral Ovarian Lymphangioma (Lymphangioleiomyoma) : International Journal of Gynecologic Pathology
Abstract
Lymphangiomas of the ovary are rare and are usually
unilateral. We present a 50-yr-old patient who presented with irregular
bleeding secondary to multiple uterine leiomyomas who was found to have
bilateral ovarian lymphangiomas. There was no evidence of pelvic
lymphatic obstruction or of lymphadenopathy, and this appeared to
exclude the possibility of acquired lymphangiectasia. The ovarian tumors
were associated with a prominent smooth muscle cell component that
partly surrounded many of the dilated vascular spaces to the extent that
the diagnoses of lymphangioleiomyoma and lymphangioleiomyomatosis were
also considered. However, there was no clinical evidence of
lymphangioleiomyomatosis in other sites and the smooth muscle cells did
not express melanocytic markers immunohistochemically. Lymphangioma and
lymphangioleiomyoma should be considered in the differential diagnosis
of bilateral, multicystic ovarian neoplasms.
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