| Literature DB >> 35518547 |
Christopher M Stevens1, Deven Champaneri2, Daniel Harper3, Assala Aslan3, Kevin Malone4, Aliaksandr Aksionau5, Naveen K Gunji1.
Abstract
Preoperative embolization of hypervascular bone metastasis is an effective measure for reducing blood loss during open orthopedic surgery. When the clinician is experienced with the procedure, the risks of the procedure are minimal and final outcomes are typically good. In this study, we report a case of a 50-year-old female patient who presented with a delayed metastatic renal cell tumor in the left proximal femur one year after radical nephrectomy. The patient underwent an effective preoperative embolization, which resulted in a remarkable absence of bleeding and a successful response subsequent to surgical fixation.Entities:
Keywords: blood loss; bone metastasis; interventional radiology; pre-operative embolization; renal cell carcinoma
Year: 2022 PMID: 35518547 PMCID: PMC9064120 DOI: 10.7759/cureus.23788
Source DB: PubMed Journal: Cureus ISSN: 2168-8184
Figure 1Coronal MRI of the pelvis, STIR sequence, demonstrating a destructive and infiltrating lesion in the left proximal femur (*) with periosteal reaction and bone edema.
STIR, short tau inversion recovery
Figure 2Fluoroscopic intraoperative image of the left femur showing no residual opacification of feeding vessels (*) to the metastatic lesion. The pathologic left proximal femur fracture (**) is also well seen.
Figure 3Histopathological finding of the biopsied lesion.
(A) Hematoxylin and eosin staining of the tumor cells. A microphotograph represents focally necrotic (*) sheets of pleomorphic epithelioid tumor cells invading the bone (→) and replacing the bone marrow, which is not present. The nuclei of tumor cells are hyperchromatic, irregular-shaped with focally prominent nucleoli. Multinucleated osteoclasts (►) are seen near the rim of the bone. (Hematoxylin and Eosin staining, 100x). (B) AE1/AE3 immunostaining of the tumor cells. The tumor cells show focally strong cytoplasmic positivity for pancytokeratin supporting epithelial differentiation (AE1/AE3 immunostaining, 200x). (C) CAM 5.2 immunostaining of the tumor cells. The tumor cells show diffusely strong cytoplasmic positivity for low molecular weight cytokeratin, further confirming the epithelial nature of the tumor cells (CAM 5.2 immunostaining, 200x). (D) PAX-8 immunostaining of the tumor cells. The urothelial origin of the tumor cells is confirmed by focally strong nuclear expression of PAX-8 (PAX-8 immunostaining, 200x). (E) CD10 immunostaining of the tumor cells. The renal nature of the tumor cells is supported by focally strong membranous positivity for CD10 (CD10 immunostaining, 200x). (F) CAIX immunostaining of the tumor cells. A focally positive membranous expression of carbonic anhydrase IX by tumor cells further supports its renal nature (CAIX immunostaining, 200x).