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Primary leiomyosarcoma of the great saphenous vein: A case report.
Tresgallo-Parés, Ruben; De Virgilio-Salgado, Lucas; Torres-Lugo, Norberto J; Asenjo-Molina, Natalia A; Ramirez, Norman; Bibiloni-Rodríguez, Juan.
Afiliação
  • Tresgallo-Parés R; Orthopaedic Surgery Department, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico 00936-5067.
  • De Virgilio-Salgado L; Orthopaedic Surgery Department, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico 00936-5067. Electronic address: lucas.devirgilio@upr.edu.
  • Torres-Lugo NJ; Orthopaedic Surgery Department, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico 00936-5067. Electronic address: norberto.torres1@upr.edu.
  • Asenjo-Molina NA; School of Medicine, University of Puerto Rico, Medical Sciences Campus, San Juan Puerto Rico 00936-5067. Electronic address: natalia.asenjo@upr.edu.
  • Ramirez N; Department of Pediatric Orthopaedic Surgery, Mayagüez Medical Center, Mayagüez, Puerto Rico 00680.
  • Bibiloni-Rodríguez J; Orthopaedic Surgery Department, University of Puerto Rico, Medical Sciences Campus, San Juan, Puerto Rico 00936-5067.
Int J Surg Case Rep ; 88: 106565, 2021 Nov.
Article em En | MEDLINE | ID: mdl-34741863
ABSTRACT
INTRODUCTION AND IMPORTANCE Vascular smooth muscle sarcomas are rare neoplasms that comprise less than 2% of all leiomyosarcomas. These malignancies usually originate in the inferior vena cava, with a limited number of cases affecting the great saphenous vein. Due to the limited reports on these sarcomas, epidemiologic data remains insufficient. CASE PRESENTATION We report the case of a 67-year-old Hispanic female that presented with an asymptomatic growing mass in her right thigh. She was managed with an En bloc resection under the impression of a smooth muscle vascular sarcoma. The diagnosis was confirmed after histopathologic evaluation. CLINICAL

DISCUSSION:

Vascular leiomyosarcomas remain a rare and challenging diagnosis. They usually present as a slowly growing mass that is initially asymptomatic. High clinical suspicion and a comprehensive radiologic evaluation, including magnetic resonance imaging, are crucial. Histopathological evaluation is essential for diagnostic confirmation. Surgical excision remains the treatment of choice, with radiation therapy mostly considered for local disease control. Postsurgical surveillance is necessary every three months to monitor for signs of recurrence.

CONCLUSION:

Physicians should remain aware of the nonspecific presentation of leiomyosarcomas and the importance of a comprehensive diagnostic approach. Early diagnosis and adequate management are fundamental elements in the treatment of these aggressive tumors.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Tipo de estudo: Screening_studies Idioma: En Revista: Int J Surg Case Rep Ano de publicação: 2021 Tipo de documento: Article