Leiomyosarcoma of the Adrenal vein: A novel approach to surgical resection

被引:16
作者
Wang T.S. [1 ]
Ocal I.T. [2 ]
Salem R.R. [3 ]
Elefteriades J. [4 ]
Sosa J.A. [1 ,3 ]
机构
[1] Department of Surgery, Section of Endocrine Surgery, Yale University School of Medicine, New Haven, CT
[2] Department of Pathology, Yale University School of Medicine, New Haven, CT
[3] Department of Surgery, Section of Oncologic Surgery, Yale University School of Medicine, New Haven, CT
[4] Department of Cardiothoracic Surgery, Yale University School of Medicine, New Haven, CT
关键词
Adrenal Gland; Inferior Vena Cava; Leiomyosarcoma; Adrenocortical Carcinoma; Adrenal Vein;
D O I
10.1186/1477-7819-5-109
中图分类号
学科分类号
摘要
Background: Leiomyosarcomas typically originate within smooth muscle cells. Leiomyosarcomas arising from the adrenal vein are rare malignancies associated with delayed diagnosis and poor prognosis. The most common vascular site of origin is the inferior vena cava. Case presentation: This is a 64-year old woman who presented with a 13 × 6.5 × 6.6 cm heterogeneous mass arising in the region of the right adrenal gland and extending into the inferior vena cava (IVC) and the right atrium. Biochemical evaluation excluded a functional tumor of the adrenal gland, and multiple tumor markers were negative. We present the novel use of deep hypothermic circulatory arrest (DHCA) in the resection of an adrenal vein leiomyosarcoma extending into the right atrium. The patient remains free of disease ten months after surgery. DHCA afforded a bloodless operative field for optimal resection of disease from within the IVC. Conclusion: The diagnosis of leiomyosarcomas of the adrenal vein is one of exclusion and involves preoperative radiological imaging and biochemical evaluation to exclude other functional tumors of the adrenal gland. Aggressive surgical resection is associated with improved survival and may be best achieved via collaboration among different surgical subspecialties. © 2007 Wang et al; licensee BioMed Central Ltd.
引用
收藏
相关论文
共 17 条
[1]  
Dew J., Hansen K., Hammon J., McCoy T., Levine E.A., Shen P., Leiomyosarcoma of the inferior vena cava: Surgical management and clinical results, Am Surg, 71, 6, pp. 497-501, (2005)
[2]  
Keiffer E.A.M., Piette J.C., Cacoub P., Chiche L., Leiomyosarcoma of the Inferior Vena Cava: Experience in 22 Cases, Ann Surg, 244, 2, pp. 289-295, (2006)
[3]  
Lack E.E., Graham C.W., Azumi N., Bitterman P., Rusnock E.J., O'Brien W., Lynch J.H., Primary leiomyosarcoma of adrenal gland. Case report with immunohistochemical and ultrastructural study, Am J Surg Pathol, 15, 9, pp. 899-905, (1991)
[4]  
Choi S.H., Liu K., Leiomyosarcoma of the adrenal gland and its angiographic features: A case report, J Surg Oncol, 16, 2, pp. 145-148, (1981)
[5]  
Zetler P.J., Filipenko J.D., Bilbey J.H., Schmidt N., Primary adrenal leiomyosarcoma in a man with acquired immunodeficiency syndrome (AIDS). Further evidence for an increase in smooth muscle tumors related to Epstein-Barr infection in AIDS, Arch Pathol Lab Med, 119, 12, pp. 1164-1167, (1995)
[6]  
Boman F., Gultekin H., Dickman P.S., Latent Epstein-Barr virus infection demonstrated in low-grade leiomyosarcomas of adults with acquired immunodeficiency syndrome, but not in adjacent Kaposi's lesion or smooth muscle tumors in immunocompetent patients, Arch Pathol Lab Med, 121, 8, pp. 834-838, (1997)
[7]  
Nakaish M.I.T., Nishio S., Yokoyama M., Spontaneous retroperitoneal hemorrhage from an adrenal leiomyosarcoma: A case report, Nishinihon J Urol, 61, pp. 466-467, (1999)
[8]  
Matsui Y., Fujikawa K., Oka H., Fukuzawa S., Takeuchi H., Adrenal leiomyosarcoma extending into the right atrium, Int J Urol, 9, 1, pp. 54-56, (2002)
[9]  
Thamboo T.P., Liew L.C., Raju G.C., Adrenal leiomyosarcoma: A case report and literature review, Pathology, 35, 1, pp. 47-49, (2003)
[10]  
Kato T., Kato T., Sakamoto S., Kobayashi T., Ikeda R., Nakamura T., Akakura K., Hikage T., Inoue T., Primary adrenal leiomyosarcoma with inferior vena cava thrombosis, Int J Clin Oncol, 9, 3, pp. 189-192, (2004)