Thanasa Anna, Thanasa Efthymia, Kamaretsos Evangelos, Grapsidi Vasiliki, Xydias Emmanouil, Ziogas Apostolos, Gerokostas Evangelos-Ektoras, Antoniou Ioannis-Rafail, Paraoulakis Ioannis, Thanasas Ioannis
Department of Health Sciences, Medical School, Aristotle University of Thessaloniki, 54124 Thessaloniki, Greece.
Department of Obstetrics and Gynecology, General Hospital of Trikala, 42100 Trikala, Greece.
Med Int (Lond). 2023 Dec 1;4(1):2. doi: 10.3892/mi.2023.126. eCollection 2024 Jan-Feb.
Intraligamental leiomyomas of the uterus are rare. Extremely rare are the huge intraligamental fibroids (>20 cm), whose pre-operative diagnosis and surgical management poses a challenge to everyday clinical practice. The present study describes the case of patient who was subjected to surgical treatment for a huge intraligamental leiomyoma of the uterus, which weighed 3,370 g. A 48-year-old patient, without menstrual disorders and with a medical history of atypical symptoms from the digestive tract, was referred for a gynecological examination. Upon a physical examination, the abdomen was found to be bloated and distended, with no signs of peritoneal irritation. An intra-abdominal mass was suspected, the upper margin of which was palpable at about the level of the xiphoid process. The findings of computed tomography and magnetic resonance imaging confirmed the presence of a huge intra-abdominal mass, which probably originated from the internal genital organs. Following consultation with the patient, surgical treatment with laparotomy was decided. Intraoperatively, a large pedunculated subserosal leiomyoma was found, arising from the right lateral wall of the uterus with retroperitoneal extension within the leaves of broad ligament. Following the resection of the intraligamental leiomyoma, which had significant surgical challenges, a total hysterectomy with bilateral adnexectomy was performed. The post-operative course was smooth. In addition, in the present study, a brief review of intraligamental leiomyomas of the uterus is presented, emphasizing the significant diagnostic and surgical challenges and potential intraoperative complications that may arise in the management of patients with this condition.
子宫韧带内平滑肌瘤较为罕见。巨大的子宫韧带内肌瘤(>20 cm)极为罕见,其术前诊断和手术处理对日常临床实践构成挑战。本研究描述了一例因重达3370 g的巨大子宫韧带内平滑肌瘤接受手术治疗的患者病例。一名48岁患者,无月经紊乱,有消化道非典型症状病史,前来接受妇科检查。体格检查时,发现腹部膨隆,无腹膜刺激征。怀疑有腹腔内肿块,其上限可在剑突水平触及。计算机断层扫描和磁共振成像结果证实存在一个巨大的腹腔内肿块,可能起源于内生殖器。与患者协商后,决定行剖腹手术治疗。术中发现一个带蒂的大浆膜下平滑肌瘤,起源于子宫右侧壁,在阔韧带叶内有腹膜后延伸。在切除具有重大手术挑战的韧带内平滑肌瘤后,行全子宫切除术加双侧附件切除术。术后过程顺利。此外,本研究还对子宫韧带内平滑肌瘤进行了简要综述,强调了在处理此类患者时可能出现的重大诊断和手术挑战以及潜在的术中并发症。