Delayed Clinical Manifestation of Malignant Potential in a Cortisol-Secreting Adrenal Tumor Initially Diagnosed as Adenoma

皮质醇分泌性肾上腺肿瘤恶性潜能的延迟临床表现,最初诊断为腺瘤

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Abstract

INTRODUCTION: Distinguishing adrenocortical carcinoma (ACC) from adenoma is often difficult, particularly in hormonally active tumors with borderline histologic features. CASE PRESENTATION: A 55-year-old woman presented with abdominal distension and central obesity. Hormonal evaluation confirmed ACTH-independent Cushing's syndrome. Imaging revealed a 60-mm left adrenal mass. Laparoscopic adrenalectomy was performed; pathology was initially interpreted as cortical adenoma with mild nuclear atypia and a Ki-67 labeling index of 6%. The patient remained disease-free until year three postoperatively when rising cortisol levels and surveillance imaging revealed a 36-mm retroperitoneal mass. Open nephrectomy and tumor excision were performed. Histopathology confirmed ACC. Retrospective review of the initial specimen revealed features consistent with early carcinoma. CONCLUSION: This case illustrates that cortisol-producing adrenal tumors initially diagnosed as adenomas may harbor unrecognized malignant potential, which can become clinically evident several years after surgery.

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