Prayson R A, Goldblum J R, Hart W R
Department of Anatomic Pathology, Cleveland Clinic Foundation, Ohio 44195, USA.
Am J Surg Pathol. 1997 Apr;21(4):383-91. doi: 10.1097/00000478-199704000-00003.
Epithelioid smooth-muscle tumors of the uterus are uncommon neoplasms for which prognostic factors have not been well established. A retrospective follow-up study of 18 uterine epithelioid smooth-muscle tumors was performed. Patients ranged in age from 27 to 83 years (mean, 45 years) and were separated into three groups based on the nuclear grade of the epithelioid tumor cells. Two tumors had grade 1 nuclei; both were examples of intravenous leiomyomatosis. They had highest mitosis counts of 1 and 3 mitotic figures (MF)/10 high-power fields (HPF), no tumor cell necrosis was found, and both patients were alive with no evidence of disease at 64 and 5 months' follow-up. Ten tumors had grade 2 nuclei. All had highest mitosis counts of 0 to 3 MF/10 HPF, except one (5 MF/10 HPF). Tumor cell necrosis was absent in nine and only one had an infiltrative border. Tumor size ranged from 1.5 to 14 cm. Two tumors contained pleomorphic ("symplastic") multinucleated giant cells similar to those seen in bizarre leiomyomas. All nine patients with follow-up were alive with no evidence of disease 5 to 203 months postoperatively (median, 74 months). One patient had also received adjuvant radiation therapy. Six tumors had grade 3 nuclei. Highest mitosis counts of 4 to 9 MF/10 HPF were found in five; one had 1 MF/10 HPF. Maximum tumor size ranged from 4.5 to 13 cm. Two had tumor cell necrosis, and two had an infiltrative border. Two of these patients died of tumor 11 and 132 months postoperatively. The former had widespread metastases at initial surgery (stage IVb); the latter patient (stage I) developed the first of seven tumor recurrences 3 years postoperatively. Both patients had also received adjuvant chemotherapy. Of the remaining four patients, two were alive with no evidence of disease at 48 and 83 months, one was alive (tumor status unknown) at 28 months, and one was lost to follow-up. Based on our findings and those in the literature, we conclude that uterine smooth-muscle tumors with a predominance of epithelioid cells are extremely uncommon and metastasize infrequently. No single histologic feature is predictive of metastatic potential. Clinically malignant tumors (i.e., epithelioid leiomyosarcomas) typically have the combination of significant nuclear atypia (either grade 2 or grade 3 nuclei) and some mitotic activity (usually at least 3 to 4 MF/10 HPF); most also have tumor cell necrosis.
子宫上皮样平滑肌瘤是一种罕见的肿瘤,其预后因素尚未完全明确。我们对18例子宫上皮样平滑肌瘤进行了回顾性随访研究。患者年龄在27岁至83岁之间(平均45岁),根据上皮样肿瘤细胞的核分级分为三组。2例肿瘤细胞核分级为1级;二者均为静脉内平滑肌瘤病的实例。其最高有丝分裂计数分别为1和3个有丝分裂象(MF)/10个高倍视野(HPF),未发现肿瘤细胞坏死,两名患者在随访64个月和5个月时均存活且无疾病证据。10例肿瘤细胞核分级为2级。除1例(5 MF/10 HPF)外,其余所有肿瘤的最高有丝分裂计数均为0至3 MF/10 HPF。9例无肿瘤细胞坏死,仅1例有浸润性边界。肿瘤大小为1.5至14 cm。2例肿瘤含有多形性(“合体性”)多核巨细胞,类似于奇异平滑肌瘤中所见。所有9例接受随访的患者术后5至203个月均存活且无疾病证据(中位时间74个月)。1例患者还接受了辅助放疗。6例肿瘤细胞核分级为3级。5例的最高有丝分裂计数为4至9 MF/10 HPF;1例为1 MF/10 HPF。最大肿瘤大小为4.5至13 cm。2例有肿瘤细胞坏死,2例有浸润性边界。这2例患者分别在术后11个月和132个月死于肿瘤。前者在初次手术时已有广泛转移(IVb期);后者(I期)术后3年出现7次肿瘤复发中的首次复发。两名患者均接受了辅助化疗。其余4例患者中,2例在48个月和83个月时存活且无疾病证据,1例在28个月时存活(肿瘤状态未知),1例失访。根据我们的研究结果及文献报道,我们得出结论,以上皮样细胞为主的子宫平滑肌瘤极为罕见,转移少见。没有单一的组织学特征可预测转移潜能。临床上的恶性肿瘤(即上皮样平滑肌肉瘤)通常具有明显的核异型性(核分级为2级或3级)和一定的有丝分裂活性(通常至少3至4 MF/10 HPF)的组合;大多数还伴有肿瘤细胞坏死。