Chordomas are rare, locally aggressive notochordal tumors, which most frequently occur in the neuraxis. We describe the case of a 74-year-old male with a history of renal cell carcinoma, who presented with a slowly enlarging mass in his left leg. While the clinical history and imaging suggested metastatic renal cell carcinoma, immunohistochemical staining with brachyury ultimately made the diagnosis of extra-axial chordoma. At 74 years of age, our patient is the oldest ever reported with bony extra-axial chordoma objectively confirmed by brachyury staining. A detailed case discussion and a review of the available literature on this rare clinicopathologic entity are provided.
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http://dx.doi.org/10.1007/s00256-017-2711-9 | DOI Listing |
Int J Surg Pathol
November 2024
Geisel School of Medicine at Dartmouth, Hanover, NH, USA.
Surg Neurol Int
October 2024
Department of Neurosurgery, National Institute of Neurology and Neurosurgery, Tlalpan, Mexico.
Background: Chordomas are primary bone tumors derived from the embryonic notochord. They represent 1-4% of all malignant bone tumors. They have a predominantly extra-axial location, arising in the clival region in 35% of reported cases.
View Article and Find Full Text PDFVirchows Arch
April 2024
The Sikl Department of Pathology, Faculty of Medicine and University Hospital in Pilsen, Charles University, Prague, Czech Republic.
Cureus
June 2023
Radiology, Jichi Medical University, School of Medicine, Tochigi, JPN.
Chordomas are rare, locally aggressive, primary bone tumors derived from primitive notochord remnants. They almost always arise within the axial skeleton, particularly in the skull base and the sacrococcygeal region. They usually present as extradural tumors, but rarely, they present as entirely intradural tumors.
View Article and Find Full Text PDFZhonghua Bing Li Xue Za Zhi
January 2023
Department of Pathology, the People's Hospital of Jiangsu Province (the First Affiliated Hospital of Nanjing Medial University), Nanjing 210029, China.
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