Zhang Zhuo, Jin Xuemei, Guo Yuzhu, Li Xiaoyu, Xu Kaixuan, Jin Guangyu
Department of Radiology, Affiliated Hospital of Yanbian University, Yanji, Jilin 133000, P.R. China.
Department of Pathology, Affiliated Hospital of Yanbian University, Yanji, Jilin 133000, P.R. China.
Oncol Lett. 2024 May 17;28(1):329. doi: 10.3892/ol.2024.14462. eCollection 2024 Jul.
Pheochromocytoma is a tumor of the sympathetic nervous system, characterized by atypical symptoms and signs. Pheochromocytoma metastases can be found in various tissues and organs. However, synchronous metastasis at the initial diagnosis of pheochromocytoma is rare. The present study described a case with synchronous liver metastasis at the initial diagnosis of adrenal pheochromocytoma based on imaging findings. A 41-year-old woman presented with liver pain and fatigue for 1 month. Physical examination showed increased blood pressure and heart rate with sinus tachycardia. Laboratory examination revealed normal levels of liver tumor markers and increased levels of serum or urine epinephrine and norepinephrine. CT examination revealed a large cystic solid mass in the right lobe of the liver and right adrenal gland, and the solid part of the mass was enhanced after enhancement. The pathological diagnosis was pheochromocytoma of the right adrenal gland with liver metastasis. The patient underwent right hepatectomy and right adrenal tumor resection. During the postoperative follow-up, the patient's blood pressure and catecholamine levels were within the normal range. Three years after surgery, the CT examination revealed multiple liver metastases. Chemotherapy was administered to the patient. A year later, re-examination revealed an increase and enlargement of the metastases, and the mass of the right adrenal gland remained similar to the previous one. After 6 months of follow-up, the patient succumbed to recurrence and metastasis. Preoperative diagnosis of metastatic pheochromocytoma is challenging. This case mainly emphasizes that imaging findings can help the clinical diagnosis of metastatic pheochromocytoma.
嗜铬细胞瘤是一种交感神经系统肿瘤,具有非典型症状和体征。嗜铬细胞瘤转移可发生于各种组织和器官。然而,嗜铬细胞瘤初诊时出现同步转移的情况较为罕见。本研究基于影像学表现描述了一例肾上腺嗜铬细胞瘤初诊时即发生同步肝转移的病例。一名41岁女性因肝区疼痛和乏力1个月就诊。体格检查显示血压升高、心率加快伴窦性心动过速。实验室检查显示肝脏肿瘤标志物水平正常,血清或尿肾上腺素和去甲肾上腺素水平升高。CT检查显示肝脏右叶和右肾上腺有一个大的囊实性肿块,增强后肿块实性部分强化。病理诊断为右肾上腺嗜铬细胞瘤伴肝转移。患者接受了右肝切除术和右肾上腺肿瘤切除术。术后随访期间,患者血压和儿茶酚胺水平在正常范围内。术后三年,CT检查显示肝脏多发转移。对患者进行了化疗。一年后复查显示转移灶增大增多,右肾上腺肿块与之前相似。随访6个月后,患者因复发转移死亡。转移性嗜铬细胞瘤的术前诊断具有挑战性。该病例主要强调影像学表现有助于转移性嗜铬细胞瘤的临床诊断。