巨大的无功能肾上腺皮质癌

I. Fam, Decky Kasman, Dilino Ryan Guntoro, Isdiyanto Septiadi
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摘要

目的:本研究的目的是报告一例51岁的男性谁被转介到我们的泌尿科,并被诊断为无功能的巨大ACC。病例报告:病例报告描述了一名51岁的印度尼西亚男性,他以持续的左上腹部不适来我科就诊,之前被误诊为消化不良。他被诊断为无功能肾上腺皮质癌,并接受了开放式肾上腺切除术。讨论:虽然患者51岁,肿瘤已明显增大,但未发现淋巴结受累或转移,切除边缘呈阴性。本例患者肾上腺功能检查结果正常。这使我们怀疑是一个无功能的肾上腺肿瘤。CT头颅、胸部和骨骼检查的转移性检查结果均为阴性。术后活检结果证实了ACC的诊断。结论:ACC是一种罕见的侵袭性肿瘤,恶性,预后差。本例非分泌性肿块诊断较晚,表现为腹部左上象限肿块效应症状,之前被误诊为消化不良症状。肾上腺肿块的功能检查有助于确定其非功能状态。ACC的早期诊断和早期手术切除有助于提高患者的总生存率。关键词:功能障碍,肾上腺皮质癌,肾上腺切除术,病例报告。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
GIANT NON-FUNCTIONING ADRENOCORTICAL CARCINOMA
Objective: This study aims to report a case of a 51 year old male who was referred to our Department of Urology and was diagnosed with a nonfunctioning giant ACC. Case(s) Presentation: The case report describes a 51-year-old Indonesian man who presented to our department with complaints of persistent upper left abdomen discomfort, previously misdiagnosed as dyspepsia. He was diagnosed as having non-functioning adrenocortical carcinoma and underwent open adrenalectomy. Discussion: Although the patient is 51 years old and the tumor has grown to a signify cant size, no lymph node involvement or metastases was found and resection margins were found to be negative. In our patient, functional adrenal work-up results were normal. This has led us to suspect a non-functioning adrenal tumor. Metastatic work-up with CT cranial, chest, and bone survey were performed, with negative result. The biopsy result after resection confirmed the diagnosis of ACC. Conclusion: ACC is a rare aggressive tumor, malignant with poor prognosis. In our case, the non-secretory mass was diagnosed late by manifestation of mass effect symptoms in the upper left quadrant of the abdomen and was previously misdiagnosed as symptoms of dyspepsia. The functional work-up of adrenal masses helped in the determination of its non-functional status. Early diagnosis of ACC and early surgical excision helps in improving the overall survival rate of the patient. Keywords: Non-functioning, adrenocortical carcinoma (ACC), adrenalectomy, case report.
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