Zanelli M, Cortecchia S, Folicaldi S, Pasquinelli G, Bondi A
Istituto di Anatomia Patologica, Azienda USL di Imola, Ospedale Vecchio, Viale Amendola 2, I-40026 Imola, Italia.
Pathologica. 2002 Aug;94(4):196-200. doi: 10.1007/s102420200031.
Cellular fibromas of the ovary are rare neoplasms belonging to the group of sex-cord stromal tumours. They have been described to show from 1 to 3 mitotic figures per 10 high power fields (HPF) and they generally behave in a benign fashion. Herein we describe the clinicopathological features of a case of ovarian cellular fibroma. The patient, a 22-year-old woman, presented with acute abdominal pain. Laparotomy revealed a large ovarian mass. Histologically the lesion was composed of spindle cells showing slight or moderate pleomorphism and 3 mitoses per 10 HPF. The spindle cells were immunoreactive for vimentin, smooth muscle actin and inhibin alpha-subunit. The differential diagnoses that we considered included the mitotically active leiomyoma because of the strong positivity for smooth muscle actin, but positive immunoreaction with anti alpha-inhibin antibody helped in confirming a sex-cord stromal tumour. Electron microscopy did not show any evidence of smooth muscle differentiation.
卵巢细胞性纤维瘤是一种罕见的肿瘤,属于性索间质肿瘤。据描述,每10个高倍视野(HPF)中可见1至3个有丝分裂象,通常表现为良性。在此,我们描述一例卵巢细胞性纤维瘤的临床病理特征。患者为一名22岁女性,表现为急性腹痛。剖腹探查发现一个巨大的卵巢肿物。组织学上,病变由梭形细胞组成,梭形细胞有轻度或中度多形性,每10个HPF中有3个有丝分裂象。梭形细胞对波形蛋白、平滑肌肌动蛋白和抑制素α亚基呈免疫反应阳性。我们考虑的鉴别诊断包括因平滑肌肌动蛋白强阳性而具有活跃有丝分裂的平滑肌瘤,但抗α抑制素抗体的阳性免疫反应有助于确诊为性索间质肿瘤。电子显微镜检查未显示任何平滑肌分化的证据。