Sengottaiyan Jagadheeswari, Balasubramanian Archana, Gunabooshanam Barathi
Pathology, Sri Ramachandra Institute of Higher Education and Research, Chennai, IND.
Cureus. 2025 May 31;17(5):e85124. doi: 10.7759/cureus.85124. eCollection 2025 May.
Introduction Leiomyosarcoma (LMS) is a malignant tumor of smooth muscle origin, most prevalent in soft tissues and the gynecologic tract. The molecular alteration associated with this condition is genomic instability, leading to complex genotypes. Aim This study aimed to study the demographic and histopathological profile of LMS cases (80 cases) diagnosed in our hospital over seven years. Materials and methods This is a retrospective study of histologically proven LMS cases from January 2017 to December 2023 using the laboratory information system from our institution. The variables to be studied included clinical demographic data and histopathological findings. Results Out of 80 cases studied, 45 were resected specimens, 25 were biopsies, and 10 were referral cases. Fifty-eight out of 80 cases were primary LMS, 17 were metastases from various sites, and five were recurrent lesions. The most common site of primary lesion was the uterus, with 26% (n=15), followed by the retroperitoneum, with 21% (n=12), and the thigh, with 12% (n=7). Infrequent sites included the prostate, intestine, omentum, kidney, and testis, each constituting about 2% (n=1), with a male:female ratio of 1:1.7 and a mean age of presentation of 55 years. The average size of the excised tumor ranged from 5.5 cm to 15 cm, and around 73% presented with histological grade 2. Almost all the cases tested for immunohistochemical (IHC) expression of smooth muscle actin (SMA) and desmin showed positivity, along with a median Ki-67 labeling index of 30%. Metastatic lesions were found primarily in the liver, lungs, and soft tissues and rarely in bone. Conclusion The results of our study witnessed the incidence of LMS at diverse anatomical locations and dimensions along with advanced grade at presentation that determined the overall prognosis, though uterine LMS tend to be more aggressive and are prone to metastasize. Hence, the comprehensive assessment at the time of diagnosis, along with close follow-up of the patients, is recommended for early detection and management of metastatic lesions.
引言
平滑肌肉瘤(LMS)是一种起源于平滑肌的恶性肿瘤,最常见于软组织和生殖道。与这种疾病相关的分子改变是基因组不稳定,导致复杂的基因型。
目的
本研究旨在研究我院七年间诊断的80例LMS病例的人口统计学和组织病理学特征。
材料和方法
这是一项回顾性研究,使用我院的实验室信息系统,对2017年1月至2023年12月组织学确诊的LMS病例进行研究。研究的变量包括临床人口统计学数据和组织病理学结果。
结果
在研究的80例病例中,45例为切除标本,25例为活检标本,10例为转诊病例。80例病例中58例为原发性LMS,17例为来自不同部位的转移瘤,5例为复发病变。原发性病变最常见的部位是子宫,占26%(n = 15),其次是腹膜后,占21%(n = 12),大腿占12%(n = 7)。少见部位包括前列腺、肠道、大网膜、肾脏和睾丸,各占约2%(n = 1),男女比例为1:1.7,平均发病年龄为55岁。切除肿瘤的平均大小在5.5厘米至15厘米之间,约73%的病例组织学分级为2级。几乎所有检测平滑肌肌动蛋白(SMA)和结蛋白免疫组化(IHC)表达的病例均呈阳性,Ki-67标记指数中位数为30%。转移瘤主要见于肝脏、肺和软组织,很少见于骨骼。
结论
我们的研究结果显示了LMS在不同解剖位置和大小的发病率,以及就诊时的高级别,这决定了总体预后,尽管子宫LMS往往更具侵袭性且易于转移。因此,建议在诊断时进行全面评估,并对患者进行密切随访,以便早期发现和处理转移瘤。