Abstract：
:Primary adrenal leiomyosarcomas (LMS) are extremely rare mesenchymal tumors. To the best of our knowledge only 12 cases (9 cases of conventional and 2 cases of pleomorphic LMS) have been reported in the literature until the present date. Herein we report a case of pleomorphic LMS in a 47-year-old woman who presented with severe abdominal pain. Computed tomography showed a large heterogeneous left adrenal mass abutting the renal vessels. The adrenal mass was resected and histopathologic examination revealed a highly pleomorphic malignant spindle cell neoplasm diffusely infiltrating the adrenal parenchyma with an immunoprofile consistent with that of a leiomyosarcoma. Clinical management and subsequent follow-up of this patient is presented.
journal_name
Urologyjournal_title
Urologyauthors
Mohanty SK,Balani JP,Parwani AVdoi
10.1016/j.urology.2007.07.029subject
Has Abstractpub_date
2007-09-01 00:00:00pages
591.e5-7issue
3eissn
0090-4295issn
1527-9995pii
S0090-4295(07)01843-2journal_volume
70pub_type
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