Qureshi Asim, Hassan Masroor, Mamoon Nadira, Ali Zafar, Ahmed Imran Nazir
Pathology Department, Shifa International Hospital, Islamabad, Pakistan.
J Pak Med Assoc. 2017 Jul;67(7):1107-1108.
This descriptive study was carried out at Pathology Department, Shifa International Hospital from 2007 to 2016; all sex cord stromal tumours diagnosed during this time period were included. Epithelial, germ cell and metastatic tumours were excluded from the study. A total of 1254 Ovarian tumours were brought to Shifa of which47 (4%) were labeled as sex cord stromal tumours. Of these 36( 76 %)were granulosa cell tumour (adult33, juvenile3), 7 were labeled as sertoli leydig cell tumours (15%), 3 as thecoma/ fibroma group (7%)and only one case was labeled as microcystic stromal tumour of the ovary (2%). Overall age range for sex cord stromal tumours was 42 (12-71). Immunohistochemistry was done in 41 out of 47 cases. Sex cord stromal tumours of the ovary are rare tumours comprising 4% of the total. Adult Granulosa cell tumour is the commonest tumour seen in our study.
这项描述性研究于2007年至2016年在希法国际医院病理科开展；纳入了在此期间诊断的所有性索间质肿瘤。上皮性肿瘤、生殖细胞肿瘤和转移性肿瘤被排除在本研究之外。共有1254例卵巢肿瘤被送至希法医院，其中47例（4%）被标记为性索间质肿瘤。在这些病例中，36例（76%）为颗粒细胞瘤（成人型33例，幼年型3例），7例被标记为支持-间质细胞瘤（15%），3例为卵泡膜瘤/纤维瘤组（7%），仅有1例被标记为卵巢微囊性间质肿瘤（2%）。性索间质肿瘤的总体年龄范围为42岁（12 - 71岁）。47例病例中有41例进行了免疫组化检查。卵巢性索间质肿瘤是罕见肿瘤，占总数的4%。成人颗粒细胞瘤是我们研究中最常见的肿瘤。
