Department of Pathology, Gynecology Service, Memorial Sloan-Kettering Cancer Center, New York, NY 10065, USA.
Am J Surg Pathol. 2011 Nov;35(11):1626-37. doi: 10.1097/PAS.0b013e31822b44d2.
In most instances, uterine smooth muscle tumors (USMTs) are readily diagnosed as either benign or malignant. Rare patients whose smooth muscle tumors fail to meet leiomyosarcoma (LMS) diagnostic criteria will experience recurrence, and occasional cases of LMS patients experience a protracted clinical disease course. The aim of this study was to investigate whether "low-grade uterine LMS" can be defined as a clinicopathological entity and to learn which histologic features of USMTs correlate with indolent prognosis. We searched institutional databases for cases diagnosed between 1982 and 2008 that had been coded as low-grade LMS and/or cases coded as LMS that were associated with recurrences after 5 years of diagnosis. There were 185 cases with available clinical follow-up data (mean follow-up for survivors was 5.4 y); 57% of patients were dead of disease (DOD), 16% of patients were alive with disease (AWD), and 24% had no evidence of disease (NED). All available slides were reviewed by 2 pathologists (E.V. and R.S.) using Stanford USMT criteria to identify cases of bona fide LMS. Cases were not excluded if they failed to meet these criteria. Nine percent (16 of 185) of tumors had been coded as low-grade LMS. On review of cases with available slides (n=16), only 4 cases (25%) met Stanford USMT criteria for LMS, and 1 additional case was a myxoid LMS. Three cases were reclassified as endometrial stromal sarcomas with smooth muscle differentiation, and 7 cases (44%) failed to meet criteria for sarcoma [ie, they were atypical smooth muscle neoplasms (ASMNs)]. Six of 16 (38%) patients were NED with a mean follow-up of 76 months; 4 of 16 (25%) patients were AWD with a mean follow-up of 102.5 months; 4 of 16 (25%) patients were DOD with a mean follow-up of 79.2 months; and 2 of 16 (12.5%) patients died of unknown causes at 104 and 120 months. Despite being coded as having low-grade LMS in the database, none of the ASMN patients died of disease. Twelve percent of all cases (n=22) were associated with late recurrences. Of the 9 cases with available slides, 5 were bona fide LMSs, and 4 were ASMNs (coded as low-grade LMS in the database and included as part of the low-grade LMS portion of this study). Five of 9 (56%) patients were NED with a mean follow-up of 214 months; 2 (22%) are AWD with a follow-up of 107 and 201 months; and 2 patients were DOD with a follow-up of 108 and 143 months. Bona fide LMS recurrences in this group were earlier (mean, 6.2 y) and frequently fatal (2 of 5), whereas those patients with recurrent ASMN experienced disease progression later (mean, 12 y), and none died of disease. Whether "low-grade" uterine LMSs indeed exist is a matter still open for debate; however, when Stanford criteria are strictly applied, all tumors classified as LMSs should be regarded as intrinsically "high grade."
在大多数情况下,子宫平滑肌肿瘤(USMT)很容易被诊断为良性或恶性。少数平滑肌肉瘤不符合平滑肌肉瘤(LMS)诊断标准的患者会复发,偶尔也会有一些 LMS 患者经历长期的临床病程。本研究旨在探讨“低度子宫 LMS”是否可以定义为一种临床病理实体,并了解哪些 USMT 的组织学特征与惰性预后相关。我们在机构数据库中搜索了 1982 年至 2008 年期间诊断为低度 LMS 和/或编码为 LMS 的病例,这些病例在诊断后 5 年内有复发。有 185 例有可用的临床随访数据(幸存者的平均随访时间为 5.4 年);57%的患者死于疾病(DOD),16%的患者患有疾病(AWD),24%的患者无疾病证据(NED)。由 2 位病理学家(EV 和 RS)使用斯坦福大学的 USMT 标准对所有可用切片进行了复查,以确定是否存在真正的 LMS。如果这些病例不符合这些标准,也不会被排除在外。9%(185 例中的 16 例)的肿瘤被编码为低度 LMS。在对有可用切片的病例(n=16)进行复查时,只有 4 例(25%)符合斯坦福大学的 LMS 标准,另有 1 例为粘液样 LMS。3 例被重新分类为具有平滑肌肉分化的子宫内膜间质肉瘤,7 例(44%)不符合肉瘤标准[即,它们是不典型平滑肌肉瘤(ASMNs)]。16 例中有 6 例(38%)患者无疾病(NED),平均随访时间为 76 个月;16 例中有 4 例(25%)患者有疾病(AWD),平均随访时间为 102.5 个月;16 例中有 4 例(25%)患者 DOD,平均随访时间为 79.2 个月;2 例(12.5%)患者在 104 个月和 120 个月时因不明原因死亡。尽管在数据库中被编码为低度 LMS,但没有一例 ASMN 患者死于疾病。12%的病例(n=22)有晚期复发。在 9 例有可用切片的病例中,5 例为真正的 LMS,4 例为 ASMN(在数据库中编码为低度 LMS,并被纳入本研究的低度 LMS 部分)。9 例中有 5 例(56%)患者无疾病(NED),平均随访时间为 214 个月;2 例(22%)为有疾病(AWD),随访时间为 107 个月和 201 个月;2 例患者为 DOD,随访时间为 108 个月和 143 个月。该组中真正的 LMS 复发较早(平均为 6.2 年),且常为致命性(5 例中有 2 例),而复发的 ASMN 患者疾病进展较晚(平均为 12 年),且无一例死于疾病。“低度”子宫 LMS 是否确实存在仍存在争议;然而,当严格应用斯坦福标准时,所有被归类为 LMS 的肿瘤都应被视为内在的“高级别”。