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Title: | Development of ipsilateral adrenocortical carcinoma sixteen years after resection of an adrenal tumour causing Cushing's syndrome | Authors: | Tan, H.S. Thai, A.C. Nga, M.E. Mukherjee, J.J. |
Keywords: | Adrenal cortex neoplasms Adrenal gland hyperfunction Neoplasm recurrence |
Issue Date: | Apr-2005 | Citation: | Tan, H.S., Thai, A.C., Nga, M.E., Mukherjee, J.J. (2005-04). Development of ipsilateral adrenocortical carcinoma sixteen years after resection of an adrenal tumour causing Cushing's syndrome. Annals of the Academy of Medicine Singapore 34 (3) : 271-274. ScholarBank@NUS Repository. | Abstract: | Introduction: At times, it may be difficult to differentiate early stage, low-grade adrenocortical carcinoma from benign adrenal adenoma. Clinical Picture: A 53-year-old lady underwent right adrenalectomy for a 4-cm adrenocortical tumour causing Cushing's syndrome. Histology revealed an adrenocortical adenoma. Sixteen years later, she presented with a 14-cm adrenal tumour, again on the right side. Treatment: She underwent surgical removal of the tumour. Histology confirmed adrenocortical carcinoma. Outcome: She died of metastatic disease 17 months later. Conclusions This case highlights the importance of long-term, systematic follow-up of patients treated for benign adrenal adenomas, especially if the tumour size exceed s 4 cm. | Source Title: | Annals of the Academy of Medicine Singapore | URI: | http://scholarbank.nus.edu.sg/handle/10635/129554 | ISSN: | 03044602 |
Appears in Collections: | Staff Publications |
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