McCluggage W G, Sloan J M, Boyle D D, Toner P G
Department of Pathology, Royal Group of Hospitals Trust, Belfast, Northern Ireland, UK.
J Clin Pathol. 1998 Nov;51(11):868-71. doi: 10.1136/jcp.51.11.868.
Malignant ovarian tumours of the fibrothecoma group are rare. The clinicopathological features of a case of ovarian malignant fibrothecoma in which there was metastatic disease in the small intestine and peritoneum at presentation are described. A number of differential diagnoses were considered but positive immunohistochemical staining of the resected ovarian and small intestinal neoplasms with anti-inhibin was of value in confirming a sex cord-stromal tumour and in excluding other lesions. The two tumours were also ultrastructurally identical. Classical malignant fibrothecomas are said to show four or more mitotic figures per 10 high power fields (HPF). Although the intestinal secondary was mitotically active, the primary ovarian tumour contained only one to two mitoses per 10 HPF, showing that formal mitotic counts are not an absolute indicator of malignant behaviour in this group of tumours.
纤维瘤组恶性卵巢肿瘤较为罕见。本文描述了一例卵巢恶性纤维瘤的临床病理特征,该病例在初诊时小肠和腹膜已有转移病灶。考虑了多种鉴别诊断,但切除的卵巢和小肠肿瘤经抗抑制素免疫组化染色呈阳性,这对于确诊性索间质肿瘤及排除其他病变具有重要价值。这两个肿瘤在超微结构上也完全相同。经典的恶性纤维瘤据报道每10个高倍视野(HPF)有4个或更多的有丝分裂象。尽管小肠转移瘤有活跃的有丝分裂,但原发性卵巢肿瘤每10个HPF仅有1至2个有丝分裂象,这表明有丝分裂计数并非该组肿瘤恶性行为的绝对指标。