Kim Mi-Jin, Park Yoon-Ki, Cho Jae-Ho
Department of Pathology, Yeungnam University College of Medicine, Daegu, Korea.
J Korean Med Sci. 2002 Dec;17(6):840-4. doi: 10.3346/jkms.2002.17.6.840.
"Cotyledonoid dissecting leiomyoma" or "Sternberg tumor" is a very rare variant of smooth muscle tumors with a distinctive gross appearance. We describe a similar lesion, probably the sixth reported case, comparing its clinicopathological features with those of previous cases. A 26-yr-old nulliparous woman underwent laparotomy for a large pelvic mass replacing the postero-lateral aspect of the uterus with extension into the left pelvic cavity in the form of numerous exophytic congested small nodules. The tumor was removed by resection without hysterectomy after frozen section examination. Histologically, there were variable sized micronodules of benign smooth muscle fascicles, which were separated by fibrous connective tissue with a marked hydropic change and rich vascularity. Immunohistochemical and ultrastructural studies were helpful for confirmation of the smooth muscle nature, but not useful for the definitive diagnosis. Due to bizarre, sarcoma-like gross appearances, this type of lesion should be subjected to frozen section examination in order to avoid overtreatment and preserve the fertility in young women.
“子叶状平滑肌瘤”或“斯滕伯格瘤”是一种非常罕见的平滑肌肿瘤变异类型,具有独特的大体外观。我们描述了一个类似的病变,可能是第六例报道的病例,并将其临床病理特征与先前病例进行比较。一名26岁未生育的女性因巨大盆腔肿块接受剖腹手术,该肿块取代了子宫后外侧部分,并以众多外生性充血小结节的形式延伸至左盆腔。在冰冻切片检查后,通过切除肿瘤而未行子宫切除术。组织学上,有大小不一的良性平滑肌束微小结节,这些结节被伴有明显水肿改变和丰富血管的纤维结缔组织分隔。免疫组织化学和超微结构研究有助于确认平滑肌性质,但对明确诊断并无帮助。由于其奇异的、肉瘤样的大体外观,这种类型的病变应进行冰冻切片检查,以避免过度治疗并保留年轻女性的生育能力。