Clinical diagnosis and treatment of adrenal cortical eosinophil tumor ( 5 cases report)
10.3760/cma.j.issn.1673-4203.2011.10.010
- VernacularTitle:肾上腺皮质嗜酸细胞肿瘤的临床诊治(附5例报告)
- Author:
Mao TANG
;
Ximei YU
- Publication Type:Journal Article
- Keywords:
Adrenal glanol neoplasms;
Eosinopnils
- From:
International Journal of Surgery
2011;38(10):677-679
- CountryChina
- Language:Chinese
-
Abstract:
Objective To study the clinical and pathological features and treatment method of adrenal cortical eosinophil tumor.Methods Retrospective analysis was made on the clinical data of 5 cases with adrenal cortical eosinophic tumor.Results Among the 5 cases,1 case looked female male-driven,1 case demonstrated cortisol dysrhythmias with cortisol increase combined Cushing syndrome,3 cases of no specific demonstrations,tumor sized 13 cm × 12 cm × 10 cm to 8.0 cm ×6.0 cm ×5.5 cm.Capsule was found complete,and no adhesion.Incision cut appeared gray,trypan-blue and cytoplasm contained rich acidophilus grain,the nuclei were large with a mild alien,fission were rare.Two cases were found immunohistochemical NSE ( + ),VIM ( + ).No relapse and metastasis were found after tumor resection.Conclusions Adrenal cortical eosinophil tumor is clinically rare,mostly being the occasional tumors.In general the tumor size is larger,more being benign tumor,growing quickly.Surgical resection is the first choice for the treatment of the disease,with good prognosis.Postoperative follow-up is needed.
