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Recurrent Metastatic Chordoma to the Liver: A Case Report and Review of the Literature. | LitMetric

AI Article Synopsis

  • Chordoma is a rare cancer originating from notochordal tissue, mainly affecting the spine and often spreading to sites like lungs and bones.
  • A case study describes a 52-year-old woman with sacral chordoma who developed a vascular liver mass, which was surgically removed but later recurred with additional metastases.
  • This is the first recorded instance of recurrent chordoma specifically involving the liver along with metastases to other areas.

Article Abstract

Chordoma is a rare malignant neoplasm derived from notochordal tissue that primarily affects the axial skeleton. Almost 40% of patients have non-cranial chordoma metastases. The most common metastatic sites are the lungs, bones, lymph nodes, and subcutaneous tissue. We present a 52-year female with a history of sacral chordoma presenting with abdominal fullness, early satiety, and a palpable abdominal mass. Abdominal magnetic resonance imaging (MRI) revealed an isolated, highly vascularized, and multilobed liver mass in the left lateral segment. The mass was surgically removed using a clean surgical margin. A histological examination and immunohistochemical staining were consistent with a metastatic chordoma. Two years later, follow-up imaging studies showed a 6.5 × 4.0 × 2.0 cm right liver lesion with multiple lungs, chest wall, pleural, and diaphragmatic lesions. Microscopic- and immunohistochemical staining revealed a recurrent metastatic chordoma. Herein, we present a unique case of metastatic recurrent chordoma in the liver with the involvement of other sites. To the best of our knowledge, no other case of recurrent liver metastasis has been reported.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9317925PMC
http://dx.doi.org/10.3390/curroncol29070367DOI Listing

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