肾上腺癌(肾上腺皮质癌)是一种罕见的癌症，一般诊断出患有肾上腺癌的时候肿瘤的体积已经很大。
Adrenal gland cancers (adrenal cortical cancer) are rare tumors that are usually very large at the time of diagnosis.
高倍镜下的肾上腺皮质癌，显示细胞的多形性、细胞核染色过深。
Here is an adrenal cortical carcinoma seen microscopically at high power to demonstrate cellular pleomorphism with nuclear hyperchromatism.
肾上腺皮质癌高倍镜图像显示，肿瘤和正常的肾上腺皮质非常相似。
This high power microscopic appearance of an adrenal cortical carcinoma demonstrates that the neoplasm closely resembles normal adrenal cortex.
方法总结15例肾上腺性征综合征患者的临床资料，其中先天性肾上腺皮质增生13例，肾上腺皮质癌2例。
Methods The clinical data of 15 patients were summarized including 13 cases of congenital adrenal hyperplasia, and 2 cases of adrenocortical carcinoma.
目的：探讨功能性肾上腺皮质癌的诊断和治疗方法。
Purpose: To study the diagnosis and treatment of functional adrenal cortical carcinoma.
方法：回顾性分析经二维及彩色多普勒超声诊断的并经手术病理证实的14例肾上腺皮质癌患者。
Method: The retrospective study was done in 14 patients with adrenal cortex carcinoma diagnosed by two dimensional and color doppler sonography and confirmed by pathology.
目的：研究肾上腺皮质癌声像图特征及其与病理结构的相关性。
Objective: To study the feature of ultrasound imaging and the correlation with pathologic structure of adrenal cortex carcinoma.
目的：研究肾上腺皮质癌声像图特征及其与病理结构的相关性。
Objective:To study the feature of ultrasound imaging and the correlation with pathologic structure in adrenal cortex carcinoma.
资料和方法回顾性分析21例肾上腺皮质癌的临床症状体征，影像学特点，手术治疗、放疗、化疗以及预后情况。
Methods : Retrospectively analyzed the clinical presentation , imaging character, surgical management , radiotherapy , chemotherapy and prognosis of 21 cases of adrenocortical carcinomas.
右侧是残余肾上腺，左边是肾上腺皮质癌。
There is residual adrenal at the right, and an adrenal cortical carcinoma is at the left.
前言： 目的：探讨儿童肾上腺皮质癌的临床特征及其诊断、治疗和预后。
Purpose:To investigate the diagnosis, treatments and prognosis of adrenal cortical carcinoma in children.
结论：影像学检查结合临床表现可以对肾上腺皮质癌作出诊断。
Conclusion: Imaging procedures are important for the diagnosis of adrenocortical carcinoma.
方法回顾性分析经病理确诊的19例肾上腺皮质癌的临床资料。
Methods Clinical data of 19 cases of adrenocortical carcinoma were retrospectively analyzed.
无功能性原发性肾上腺皮质癌甚为罕见，国内文献报告仅14例。
Non-functioning primary carcinoma of the adrenal-cotter is rare and only 14 cases repered in Chinese literatures.
结论：肾上腺皮质癌临床发病率低，手术治疗有效。
Conclusion: There is a low incidence rate of adrenal cortical carcinoma and its surgical treatment is effective.
TSP-1在正常肾上腺皮质表达明显高于肾上腺皮质癌（P＜0.01）；
The expression of TSP-1 was higher in normal adrenal cortex compared with adrenocortical carcinomas (P<0.01).
术后2年无瘤生存4例。结论早期发现、早期手术及完整切除肿瘤是提高儿童肾上腺皮质癌生存率的关键。
The 2 year survival is 4 out of 6. Conclusions Early diagnosis and complete tumor resection is the only means to achieve good survival in children with adrenocortical carcinoma.
结果：本例肾上腺皮质癌患者经后腹腔镜将肿瘤完整切除，临床症状缓解，随访半年，无复发。
Results: the tumor has been completely removed by laparoscopy for the carcinoma patient who showed improved symptoms after the surgery and no recurrence after half a year follow - up.
结果：本例肾上腺皮质癌患者经后腹腔镜将肿瘤完整切除，临床症状缓解，随访半年，无复发。
Results: the tumor has been completely removed by laparoscopy for the carcinoma patient who showed improved symptoms after the surgery and no recurrence after half a year follow - up.
应用推荐