The problem of rare tumors in gynecology: a clinical case of benign retroperitoneal sclerosing pelvic pecoma in 49-year-old woman

V. I. Lanchinsky, Y. Chushkov, A. B. Ponomarev, Y. Osmanov, A. I. Ishchenko, N. V. Vorobev
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Abstract

The tumor lesions of the reproductive system organs carry the leading position in the structure of gynecological diseases. One of the rare tumors that can affect the organs of the reproductive system is pecoma, which is a tumor of mesenchymal origin. Because of it’s rare occurrence the gynecologists often misinterpret available clinical data and the results of patient`s examination, diagnosing and treating the tumor as a myoma before having received the results of the histological examination. Our article describes a clinical case of a patient who had a preliminary diagnosis of uterine fibroids, and because of this fact the planned surgical treatment was carried out. But a retroperitoneal tumor originating from the uterine vein was detected during the surgery. The diagnosis of sclerosing pecoma was established by histological and immunohistochemical studies. The article analyzes the clinical features of the patient`s disease, as well as the available results of instrumental methods of examination which can lead to final diagnosis of pecoma, also difficult issues of diagnosis and tactics of diagnostic search are noted.The literature data on the frequency of detection of pecomas, the features of their structure are presented. It is marked, that there is also a possibility of pecoma`s localization in various organs, for example, lungs, liver, kidneys, as well as in soft tissues. The possibility of multiple lesions – pecomatosis is emphasized. It is noted that among the pelvic organs the uterus is affected most often, but furthermore, the pelvic lymph nodes, the broad ligament, the omentum, the peritoneum of the pelvis and the rectum wall can be also involved in the pathological process. Risk factor of pecomas malignancy is discussed separately, the presence of three types of pecomas is determined. This fact significantly effects the probability of relapse of the tumor after surgical removal and, respectively, the tactics of postoperative follow‑up of such patients.
妇科罕见肿瘤的问题:49岁女性良性腹膜后硬化性盆腔pecoma 1例
生殖系统器官肿瘤病变在妇科疾病结构中占据主导地位。pecoma是一种罕见的影响生殖系统器官的肿瘤,它是一种起源于间充质的肿瘤。由于其罕见,妇科医生往往会误解现有的临床资料和患者的检查结果,在没有得到组织学检查结果之前就将肿瘤诊断为肌瘤并进行治疗。我们的文章描述了一个初步诊断为子宫肌瘤的患者的临床病例,因为这个事实,计划的手术治疗是进行的。但是手术中发现了一个起源于子宫静脉的腹膜后肿瘤。通过组织学和免疫组织化学研究确定了硬化性pecoma的诊断。文章分析了患者疾病的临床特点,以及可用于最终诊断pecoma的仪器检查方法的现有结果,并指出了诊断难点和诊断搜索策略。文献资料的检测频率pecomas,他们的结构特点提出。值得注意的是,pecoma也有可能定位于不同的器官,如肺、肝、肾,以及软组织。多重病变- pecomatosis的可能性被强调。值得注意的是,在盆腔器官中,子宫是最常受影响的,此外,盆腔淋巴结、阔韧带、大网膜、骨盆腹膜和直肠壁也可参与病理过程。分别讨论了胸腺瘤恶性的危险因素,确定了胸腺瘤存在的三种类型。这一事实显著影响了手术切除后肿瘤的复发率,并分别影响了此类患者的术后随访策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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