Ben Amara Fethi, Jouini Hassen, Nasr Meher, Malek Monia, Neji Khaled, Reziga Hedi, Mrad Karima, Ben Romdhane Khaled
Department B of Obstetrics and Gynecology, CMNT, Tunisia.
Tunis Med. 2007 Jul;85(7):591-5.
Primary broad ligament leiomyosarcoma (LMS) is an extremely rare tumor with few well-documented cases. We are aware of 15 previously reported observations.
Report of a new case.
In this report we report a case of a right pelvic sidewall leiomyosarcoma with involvement of the appendix in a 49-year-old woman. A hysterectomy, bilateral salpingo-oophorectomy, omentectomy and appendicectomy were done, without complications. The patient died five months later. The case illustrates the difficulty of correct diagnosis before intervention. On this occasion, review of the literature confirms that this site remains unusual and the management is difficult.
原发性阔韧带平滑肌肉瘤（LMS）是一种极其罕见的肿瘤，仅有少数病例有充分的文献记载。我们知晓此前有15例报告病例。
报告一例新病例。
在本报告中，我们报告了一例49岁女性右侧盆腔侧壁平滑肌肉瘤累及阑尾的病例。患者接受了子宫切除术、双侧输卵管卵巢切除术、大网膜切除术和阑尾切除术，未出现并发症。患者于五个月后死亡。该病例说明了干预前正确诊断的困难。此次文献回顾证实，该部位仍然不常见，且治疗困难。
