Guilbert Marie-Christine, Samouëlian Vanessa, Rahimi Kurosh
Department of Pathology (M.-C.G., K.R.) Division of Gyneco-Oncology (V.S.), Centre hospitalier de l'Université de Montréal (CHUM), Montréal, QC, Canada.
Int J Gynecol Pathol. 2016 Jan;35(1):30-2. doi: 10.1097/PGP.0000000000000204.
Numerous histologic variants of uterine leiomyomas have been described. The main interest in recognizing these variants is differentiating them from leiomyosarcoma. Osteoclast-like giant cells (OLGC) have been described in association with leiomyosarcoma but to our knowledge, never with leiomyoma. We here report the case of a 58-year-old woman who underwent an elective total hysterectomy with bilateral salpingo-oophorectomy and bilateral pelvic lymphadenectomy for endometrial atypical complex hyperplasia. Multiple typical uterine leiomyoma were identified. One of them showed numerous OLGC admixed with fascicules of bland smooth muscle cells. No atypical features were identified in multiple sections of this otherwise classic uterine leiomyoma. The OLGC showed strong positivity for CD68. The patient, on follow-up, did not show any evidence of recurrent or metastatic disease. This unusual finding expands the morphologic spectrum of uterine leiomyomas. When confronted with a uterine smooth muscle cell tumor with an OLGC component, it is important to search for atypical features diagnostic of leiomyosarcoma.
子宫平滑肌瘤有多种组织学变异类型已被描述。认识这些变异类型的主要意义在于将它们与平滑肌肉瘤区分开来。破骨细胞样巨细胞(OLGC)已被描述与平滑肌肉瘤有关,但据我们所知,从未与平滑肌瘤相关。我们在此报告一例58岁女性,因子宫内膜非典型复杂性增生接受了择期全子宫切除术、双侧输卵管卵巢切除术及双侧盆腔淋巴结清扫术。术中发现多个典型的子宫平滑肌瘤。其中一个肌瘤显示有大量OLGC,与束状的良性平滑肌细胞混合存在。在这个其他方面典型的子宫平滑肌瘤的多个切片中未发现非典型特征。OLGC对CD68呈强阳性。随访时,该患者未显示任何复发或转移性疾病的迹象。这一不寻常的发现扩展了子宫平滑肌瘤的形态学谱。当面对一个具有OLGC成分的子宫平滑肌细胞肿瘤时,寻找诊断平滑肌肉瘤的非典型特征很重要。