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CASE REPORT article
Front. Oncol.
Sec. Genitourinary Oncology
Volume 14 - 2024 |
doi: 10.3389/fonc.2024.1461165
A Rare Case of Renal Epithelioid Angiosarcoma
Provisionally accepted- The First Affiliated Hospital, Guizhou University of Traditional Chinese Medicine, Guiyang, China
Primary renal epithelioid angiosarcoma (EAS) is extremely rare and carries a poor prognosis. Herein, we present a case of renal EAS in an 81-year-old male patient who complained of hematuria for one year. A computerized tomography (CT) scan revealed an occupying lesion at the upper pole of the left kidney, with scattered calcifications, along with retroperitoneal lymph node metastasis and possible lung metastasis. A laparoscopic palliative nephrectomy was performed, and postoperative pathology confirmed a malignant tumor with necrosis in the left kidney. Immunohistochemistry (IHC) revealed positive expression for CD31, CD10, and Vimentin, consistent with the diagnosis of EAS. Although EAS is a rare, aggressive, and often misdiagnosed condition, IHC can help confirm its diagnosis, and in our case, the scattered calcifications observed on CT imaging might be helpful in its differential diagnosis.
Keywords: scattered calcifications, Pathology, Renal, Epithelioid angiosarcoma, case report
Received: 08 Jul 2024; Accepted: 11 Nov 2024.
Copyright: © 2024 Zhai, Che, Shen, Cen, Zhang, Li, Tang and Tang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
* Correspondence:
Kaifa Tang, The First Affiliated Hospital, Guizhou University of Traditional Chinese Medicine, Guiyang, China
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