Publications by authors named "G De Pinieux"

Article Synopsis
  • Superficial leiomyosarcoma is a rare soft tissue tumor from smooth muscle cells, making up about 2-3% of superficial sarcomas, with a slight age preference for patients around 50-60 years.
  • This study analyzed 26 cases of leiomyosarcoma to understand their clinicopathological features and treatment outcomes, identifying more cases in the cutaneous subtype compared to the subcutaneous subtype.
  • Results showed that even with clear surgical margins, patients had a notable risk of recurrence and metastasis, particularly to the lungs, bones, and liver, highlighting the need for long-term monitoring.*
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Background: To better understand the importance of the New York esophageal squamous cell carcinoma 1 (NY-ESO-1) and human leukocyte antigen (HLA) subtypes in treatment decision-making, further investigation of their prevalence and prognostic impact among patients with metastatic synovial sarcoma (mSS) is needed.

Patients And Methods: This was a retrospective clinico-biological cohort study of adults with mSS. Patient data were collected from the French Sarcoma Group NetSARC database and supplemented by electronic medical records.

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Recently, FN1 fusions to receptor tyrosine kinase genes have been identified in soft tissue tumors with calcified chondroid matrix named calcifying chondroid mesenchymal neoplasms (CCMNs). We collected 33 cases of CCMN from the French network for soft tissue and bone tumors. We performed whole-exome RNA sequencing, expression analysis, and genome-wide DNA methylation profiling in 33, 30, and 20 cases of CCMN compared with a control group of tumors, including noncalcified tenosynovial giant cell tumor (TGCT).

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Angioleiomyomas are uncommon, noncancerous, smooth muscle tumors that primarily arise from blood vessels. Previous studies have yielded limited data due to the lack of interdisciplinary approaches or restricted patient pools. This study aims to provide a comprehensive analysis of angioleiomyomas, including the demographic, clinical, radiological, and histopathological features, with a large number of patients.

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