MARATTO

preprint

Epithelioid sarcoma: the challenge of providing the optimal treatment.

Abstract

Epithelioid sarcoma are rare malignant mesenchymal tumors that affect mostly young males in the distal part of extremities. They are frequently treated initially with incomplete resection because of their clinically slow-growing benign pattern. Heterogeneity in pathological presentation of epithelioid leads to frequent misdiagnosis that affects survival. This report describes the clinical course and management of a 58-year-old man who presented with epithelioid sarcoma in the shoulder girdle. The case was misdiagnosed initially as a benign lesion and then, at the local recurrence, as a carcinoma. The patient is free of recurrence and metastases 4 years after a large resection of the axillary lymph recurrence sacrificing the axillary vein followed by radiation.

Research topics

  • Sarcoma Diagnosis and Treatment
  • Vascular Tumors and Angiosarcomas
  • Cardiac tumors and thrombi

Sustainable Development Goals

Read the original research

This page summarises published work. The authoritative version sits with the publisher.

DOI: 10.22541/au.171302688.81439366/v1

Is something wrong with this record? Report it or request removal.

Discussion

Discuss this research

Have you built on this work, tried to replicate it, or seen it applied in practice? Share what you know. Verified researchers and MARATTO™ domain experts can open a discussion, and any member can reply. Contributions are reviewed before they appear.

No discussion yet. Open the first thread.