Case Report
Year 2016,
Volume: 1 Issue: 3, 134 - 136, 05.10.2017
Abstract
Leiomyosarkom retroperitondaki düz kas hücrelerinden çıkabilen nadir bir malign tümördür. Tüm yumuşak doku sarkomlarının yaklaşık %5-10 kadarını leiomyosarkomlar oluşturur. Tanı konulmadan önce sıklıkla büyük boyutlara ulaşır. Bu yazıda çok nadir olarak görülen retroperitoneal leimyosarkomlu 61 yaşındaki kadın hastayı klinik ve mikroskopik
bulgulularla sunduk.
Keywords
References
- 1. Gustafson P, Willen H, Baldetrop B Fernö M, Akerman M, Rydholm A.Soft tissue leimyosarcoma: a population based epidemiologic and prognestic study of 48 patients, including cellular DNA content. Cancer 1992 ;70: 114-9. 2. Ardoino I, Miceli R, Berselli M. Biganzoli E, Fiore M, Collini P, Stacchiotti S, Casali PG, Gronchi A. Histology spesific nomogram for primary retroperitoneal soft tissue srcoma. Cancer 2010;116:2429-36.
- 3. Campell-Walsh Üroloji, 2014; 4.cilt: üst üriner sistem kanserleri, Kısım 12, 1508.
- 4. Hueman MT, Herman JM, Ahuja N. Management of retroperitoneal sarcomas. Surg Clin North Am. 2008;88:583-97.
- 5. Gronchi A, Casali PG, Fiore M, Mariani L, Lo Vullo S, Bertulli R, Colecchia M, Lozza L, Olmi P, Santinami M, Rosai J. Retroperitoneal soft tissue srcoma; pattern of recurrence in 167 patients treated at a single institution. Cancer 2004;100:2448-55.
- 6. Bautista N, Su W, O’Connell T. Retroperitoneal soft tissue sarcomas: prognosis and treatment of primary and recurrent disease. Am Surg. 2000 Sep;66(9):832-6.
- 7. Stoeckle E, Coindre JM, Bonvalot S, Kantor G, Terrier P, Bonichon F, Nguyen Bui B; French Federation of Cancer Centers Sarcoma Group. Prognostic factors in retroperitoneal sarcomas; a multivariate analysis of a series of 165 patients of the French Cancer Center Federation Sarcoma Group. Cancer. 2001;92:359-68.
Year 2016,
Volume: 1 Issue: 3, 134 - 136, 05.10.2017
Abstract
Leiomyosarcoma a rare malignancy of smooth muscle may arise from the retroperitoneum. Of all soft tissue sarcomas approximately 5-10% are leiomyosarcomas. They often reach a large size before diagnosis is made. We present a 61 year old female patient with retroperitoneal leiomyosarcoma who was seen very rarely in this article with clinical and microscopic findings.
Keywords
References
- 1. Gustafson P, Willen H, Baldetrop B Fernö M, Akerman M, Rydholm A.Soft tissue leimyosarcoma: a population based epidemiologic and prognestic study of 48 patients, including cellular DNA content. Cancer 1992 ;70: 114-9. 2. Ardoino I, Miceli R, Berselli M. Biganzoli E, Fiore M, Collini P, Stacchiotti S, Casali PG, Gronchi A. Histology spesific nomogram for primary retroperitoneal soft tissue srcoma. Cancer 2010;116:2429-36.
- 3. Campell-Walsh Üroloji, 2014; 4.cilt: üst üriner sistem kanserleri, Kısım 12, 1508.
- 4. Hueman MT, Herman JM, Ahuja N. Management of retroperitoneal sarcomas. Surg Clin North Am. 2008;88:583-97.
- 5. Gronchi A, Casali PG, Fiore M, Mariani L, Lo Vullo S, Bertulli R, Colecchia M, Lozza L, Olmi P, Santinami M, Rosai J. Retroperitoneal soft tissue srcoma; pattern of recurrence in 167 patients treated at a single institution. Cancer 2004;100:2448-55.
- 6. Bautista N, Su W, O’Connell T. Retroperitoneal soft tissue sarcomas: prognosis and treatment of primary and recurrent disease. Am Surg. 2000 Sep;66(9):832-6.
- 7. Stoeckle E, Coindre JM, Bonvalot S, Kantor G, Terrier P, Bonichon F, Nguyen Bui B; French Federation of Cancer Centers Sarcoma Group. Prognostic factors in retroperitoneal sarcomas; a multivariate analysis of a series of 165 patients of the French Cancer Center Federation Sarcoma Group. Cancer. 2001;92:359-68.
There are 6 citations in total.
Details
| Primary Language | Turkish |
|---|---|
| Journal Section | Case report |
| Authors | |
| Publication Date | October 5, 2017 |
| Published in Issue | Year 2016 Volume: 1 Issue: 3 |
