Atypical Leiomyomas of the Uterus: A Clinicopathologic Study of 54 Cases and Immunohistochemical Analysis of Ki-67 (MIB-1) and p53.

E. Kaygusuz, H. Cetiner, H. Yavuz, C. K. Kacakusak, E. Hacıhasanoğlu, N. Dursun, C. Mesci, M. Eken
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Abstract

Objective Uterine atypical leiomyomas (AL) are extremely rare, and occurs a decade earlier than the onset of leiomyosarcoma. According to the literature, extensive clinicopathologic studies on AL are limited to only two studies. Atypical leiomyomas of uterus are well-defined neoplasms with smooth muscle cells. The aim of this study was to investigate clinicopathologic findings in 54 cases with Atypical Leiomyoma diagnosis and Ki-67 and p53 expressions immunohistochemically. Methods Fifty-four cases diagnosed between 2000 and 2013 were included. The histological and clinical features of the cases were revised and their medical records were examined. Ki-67 and p53 were performed on all cases immunohistochemically. Results The average age of cases was 41.8 years. The average clinical follow-up period was 57 months. Hysterectomy was performed in 31 cases, and myomectomy was performed in 21 cases, while resection of the mass was performed in two patients due to the intraligamenter mass. The average size of the neoplasms was 6.2 cm. Severe cellular atypia was noticed in 25 patients. While the number of mitoses was 1/10 HPF in 30 cases, it was 4/10 HPF in six of them. Ki-67 was found positive in 50 cases at the rate of 1-5% immunohistochemically, while p53 has demonstrated staining at the ratio of 10-15% staining in four patients. Conclusion The differential diagnosis of atypical leiomyomas from leiomyosarcomas is crucial. The recurrence rate after follow-up is 2%. In our opinion, the cases diagnosed with 'atypical leiomyoma with limited experience' before should be correctly diagnosed with atypical leiomyoma. We recommend that Ki-67 and p53 can be used as an adjuvant marker immunohistochemically in the cases that problem in differential diagnosis from Leiomyosarcoma exist.
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不典型子宫平滑肌瘤54例临床病理分析及Ki-67 (MIB-1)和p53的免疫组化分析。
目的子宫不典型平滑肌瘤(AL)极为罕见,其发病时间比平滑肌肉瘤早10年。根据文献,广泛的AL临床病理研究仅限于两项研究。子宫非典型平滑肌瘤是一种具有平滑肌细胞的肿瘤。本研究的目的是探讨54例非典型平滑肌瘤的临床病理表现和Ki-67和p53的免疫组织化学表达。方法纳入2000 ~ 2013年诊断的54例病例。对病例的组织学和临床特征进行了修改,并检查了他们的医疗记录。免疫组织化学检测Ki-67和p53。结果患者平均年龄41.8岁。平均临床随访期为57个月。31例行子宫切除术,21例行子宫肌瘤切除术,2例因韧带内肿物行肿物切除术。肿瘤平均大小为6.2 cm。25例患者出现严重的细胞异型性。30例有丝分裂数为1/10 HPF, 6例为4/10 HPF。50例Ki-67阳性,免疫组化率为1-5%,4例p53染色率为10-15%。结论不典型平滑肌瘤与平滑肌肉瘤的鉴别诊断至关重要。术后复发率为2%。我们认为,以前诊断为“经验有限的不典型平滑肌瘤”的病例应正确诊断为不典型平滑肌瘤。我们推荐Ki-67和p53可以作为平滑肌肉瘤鉴别诊断中存在问题的病例的辅助免疫组织化学标记物。
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