Chien Hui-Ping, Chang Yu-Sun, Hsu Pei-Sung, Lin Jen-Der, Wu Yi-Chin, Chang Hui-Lang, Chuang Cheng-Keng, Tsuei Ke-Hung, Hsueh Chuen
Department of Pathology, Chang Gung Memorial Hospital, No. 5 Fu-Shin Street, Kuei-Shan, Taoyuan, Taiwan, Republic of China.
Endocr Pathol. 2008 Winter;19(4):274-81. doi: 10.1007/s12022-008-9046-y.
Adrenal cystic lesions are uncommon and we analyzed clinical and pathologic features of 25 such cases from a single institute over 23 years. There were 16 pseudocysts, eight endothelial cysts, and one epithelial cyst. Seven of eight endothelial cysts were confirmed to be lymphangiomatous by D2-40 immunostaining. We suggest that pseudocysts and endothelial cysts may have different histogenesis. The proposed mesothelial origin of adrenal epithelial cyst cannot be confirmed in our example. Seven adrenal pseudocysts were associated with tumor, including two pheochromocytomas, one neuroblastoma, one adrenal cortical carcinoma, one adrenal cortical adenoma, one myelolipoma, and one schwannoma. The distinction of true cystic lesion from cystic neoplasm is important and requires thorough sampling of the specimens.
肾上腺囊性病变并不常见,我们分析了一家机构23年间25例此类病例的临床和病理特征。其中有16例假性囊肿、8例内皮囊肿和1例上皮囊肿。8例内皮囊肿中有7例经D2-40免疫染色证实为淋巴管瘤样。我们认为假性囊肿和内皮囊肿可能有不同的组织发生。在我们的病例中,肾上腺上皮囊肿的间皮起源假说无法得到证实。7例肾上腺假性囊肿与肿瘤相关,包括2例嗜铬细胞瘤、1例神经母细胞瘤、1例肾上腺皮质癌、1例肾上腺皮质腺瘤、1例髓脂肪瘤和1例神经鞘瘤。区分真正的囊性病变和囊性肿瘤很重要,需要对标本进行全面取材。