Diagnosis and management of retroperitoneal soft-tissue sarcoma

F. Kristian Storm*, David M. Mahvi

*Corresponding author for this work

Research output: Contribution to journalArticle

179 Scopus citations

Abstract

Retroperitoneal soft-tissue sarcomas are locally invasive tumors that remain occult for long periods and grow quite large due to the abdominal cavity's remarkable ability to accommodate these slowly expanding masses with a paucity of attendant symptoms. An open biopsy is required to establish diagnosis definitively. Despite improved imaging techniques and preoperative and intraoperative patient management, resectability has not changed significantly in the past 20 years. Even with an aggressive operative approach, only one half the tumors can be resected completely, and of those, more than 90% recur locally and result in the death of the patient. The addition of adjuvant radiotherapy or chemotherapy has not altered this pattern of local failure, in contrast to promising results with extremity soft-tissue sarcoma. Because of the rarity of these tumors, there is an urgent need to establish a national retroperitoneal sarcoma registry and to form cooperative intergroup studies to evaluate, treat, and apply innovative multimodality combination therapies to these otherwise lethal tumors.

Original languageEnglish (US)
Pages (from-to)2-10
Number of pages9
JournalAnnals of surgery
Volume214
Issue number1
StatePublished - Jan 1 1991

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ASJC Scopus subject areas

  • Surgery

Cite this

Storm, F. K., & Mahvi, D. M. (1991). Diagnosis and management of retroperitoneal soft-tissue sarcoma. Annals of surgery, 214(1), 2-10.