Angiosarcoma of the Adrenal Gland Treated Using a Multimodal Approach.
Publication/Presentation Date
1-1-2017
Abstract
Angiosarcoma of the adrenal gland is an extremely rare malignancy. We report a case of a 59-year-old female who presented with abdominal pain and profound anemia. A 7 cm enhancing, lipid-poor adrenal mass with calcifications that extended posterior to the vena cava was identified on imaging. Patient underwent right adrenalectomy with retroperitoneal lymph node dissection. Pathology demonstrated angiosarcoma of the adrenal gland. Consolidative treatment included adjuvant radiation and chemotherapy. Patient remains disease free 1.5 years following treatment. Prior reported literature on the diagnosis and management of adrenal angiosarcoma is reviewed.
Volume
10
First Page
38
Last Page
41
ISSN
2214-4420
Published In/Presented At
Fuletra, J. G., Ristau, B. T., Milestone, B., Cooper, H. S., Browne, A., Movva, S., Galloway, T. J., Lee, R., Waingankar, N., & Kutikov, A. (2016). Angiosarcoma of the Adrenal Gland Treated Using a Multimodal Approach. Urology case reports, 10, 38–41. https://doi.org/10.1016/j.eucr.2016.11.003
Disciplines
Medicine and Health Sciences
PubMedID
27920990
Department(s)
Department of Pathology and Laboratory Medicine
Document Type
Article