The diagnosis and treatment of primary adrenal lipomatous tumors in Chinese patients: a 31-year follow-up study

Authors

  • Fukang Sun Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China
  • Juping Zhao Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Xiaolong Jing Department of Pathology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Wenlong Zhou Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Xin Huang Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Haofei Wang Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Yu Zhu Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Fei Yuan Department of Pathology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai
  • Zhoujun Shen Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai

DOI:

https://doi.org/10.5489/cuaj.977

Keywords:

diagnosis, treatment, adrenal lipomatous tumors

Abstract

Introduction: Adrenal lipomatous tumours (ALTs) are rarely encountered in clinical practice and consequently little is known about their clinical features.

Methods: We analyze the clinical features, diagnosis and treatment of ALTs based on cases presenting at a single centre over a 31-year period. We reviewed clinical data from patients with primary adrenal tumours treated at the Ruijin Hospital, Shanghai between January 1980 and December 2010.

Results: A total of 73 cases of primary ALTs in 22 men and 51 women (mean age 51.1±14.2 years) were reviewed. The ALTs included 65 myelolipomas (89.0%), 3 lipomas (4.1%), 2 angiomyolipomas (2.7%), 2 teratomas (2.7%), and 1 liposarcoma (1.4%). Of the total 73 patients, 24 of them had tumours in the left adrenal gland, 47 in the right gland and 2 had bilateral tumours. In total, 51 patients underwent open surgery and 22 laparoscopic surgery.

Conclusion: Myelolipoma is predominant among the various types of lipomatous adrenal gland tumours; it accounts for about 90% of all cases. Surgery is recommended for tumours ≥3.5 cm in diameter, for all cases of symptomatic tumour, and for cases of teratoma or liposarcoma identified by preoperative imaging.

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Author Biographies

Fukang Sun, Department of Urology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China

Department of Urology, Ruijin Hospital,

Chief doctor

Xiaolong Jing, Department of Pathology, Ruijin Hospital, Shanghai JiaoTong University School of Medicine, Shanghai

chief doctor

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Published

2014-03-11

How to Cite

Sun, F., Zhao, J., Jing, X., Zhou, W., Huang, X., Wang, H., Zhu, Y., Yuan, F., & Shen, Z. (2014). The diagnosis and treatment of primary adrenal lipomatous tumors in Chinese patients: a 31-year follow-up study. Canadian Urological Association Journal, 8(3-4), e132–6. https://doi.org/10.5489/cuaj.977

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Section

Original Research