Hillesheim Paul B, Farghaly Hanan
Department of Pathology and Laboratory Medicine, University of Louisville Louisville, KY 40202, USA.
Int J Clin Exp Pathol. 2010 Oct 9;3(8):808-11.
Anaplastic carcinoma (AC) of spindle cell type is an exceedingly rare ovarian malignant neoplasm. The histo-genesis of these tumors is still controversial. Although it was first thought to carry an invariably unfavorable prognosis, recent data indicates that this does not apply to stage Ia tumors. To date, there have been less than ten cases of anaplastic spindle cell carcinoma reported in the medical literature. Furthermore, our case is the first time this tumor has been described in a 40-year-old female with malignant spindle cells merging with conventional high grade adeno-carcinoma. The differential diagnosis of spindle cell proliferation in the ovary will be discussed and their distinction using a panel of immunohistochemical stains. This report demonstrated that the findings of malignant spindle cell proliferation does not imply this entity to be carcinosarcoma. The distinction of AC from true sarcomas is important because of the poorer prognosis of the later compared with the quite favorable behavior of AC. However, such existence necessitates a careful tissue sampling for the logical distinction between AC and carcinosarcoma, which is critical for planning further management and ultimately the predictor of prognosis.
梭形细胞型间变性癌(AC)是一种极其罕见的卵巢恶性肿瘤。这些肿瘤的组织发生仍存在争议。尽管最初认为其预后总是不佳,但最近的数据表明,这并不适用于Ia期肿瘤。迄今为止,医学文献中报道的间变性梭形细胞癌病例不到十例。此外,我们的病例是首次在一名40岁女性中描述这种肿瘤,其恶性梭形细胞与传统高级别腺癌合并。将讨论卵巢中梭形细胞增殖的鉴别诊断,并使用一组免疫组化染色剂对其进行区分。本报告表明,恶性梭形细胞增殖的发现并不意味着该实体为癌肉瘤。将AC与真正的肉瘤区分开来很重要,因为后者的预后比AC的良好行为更差。然而,这种情况需要仔细进行组织采样,以便在AC和癌肉瘤之间进行合理区分,这对于规划进一步的治疗以及最终预测预后至关重要。