Weissferdt Annikka, Maheshwari Madhavi B, Downey Gabrielle P, Rollason Terence P, Ganesan Raji
Department of Histopathology, Birmingham Women's Hospital, Metchley Park Road, Edgbaston, B15 2TG, UK.
Diagn Pathol. 2007 Jun 13;2:18. doi: 10.1186/1746-1596-2-18.
Cotyledonoid dissecting leiomyoma of the uterus is a recently described rare variant of benign uterine leiomyoma. We report a case of cotyledonoid dissecting leiomyoma in a 52 year old woman who presented with menorrhagia and abdominal pain. An ultrasound scan showed a bulky uterus and a cystic heterogenous mass near the left ovary. At hysterectomy, the left broad ligament mass was removed. This was continuous with an ill-defined nodular area in the myometrial fundus. Microscopy revealed a benign smooth muscle proliferation in the myometrium that extended beyond the uterus and into the broad ligament. The lesion appeared to be dissecting the myometrial fibres and showed areas of oedema, hyalinisation and perinodular hydropic change. Cellular atypia, mitoses and coagulative necrosis were absent. The patient is alive and well 18 months after surgery. It is important to recognize this benign and unusual appearing variant of leiomyoma in order to prevent inappropriate treatment.
子宫叶状分离性平滑肌瘤是一种最近才被描述的罕见的子宫良性平滑肌瘤变体。我们报告一例52岁女性的子宫叶状分离性平滑肌瘤病例,该患者表现为月经过多和腹痛。超声扫描显示子宫增大,左卵巢附近有一个囊性不均质肿块。在子宫切除术中,切除了左侧阔韧带肿块。该肿块与子宫肌层底部一个边界不清的结节状区域相连。显微镜检查显示子宫肌层有良性平滑肌增生,延伸至子宫外并进入阔韧带。病变似乎在分离子宫肌纤维,并显示出水肿、玻璃样变和结节周围水样变性区域。未见细胞异型性、核分裂象和凝固性坏死。患者术后18个月健在。认识到这种外观良性但不寻常的平滑肌瘤变体很重要,以避免不适当的治疗。