Barinova I V, Buyanova S N, Kondrikov N I, Shchukina N A, Voloshchuk I N, Mgeliashvili M V, Petrakova S A, Aksenova A A
Moscow Regional Research Institute of Obstetrics and Gynecology, Moscow, Russia.
Arkh Patol. 2020;82(1):62-67. doi: 10.17116/patol20208201162.
To reveal the morphological characteristics of simultaneously diagnosed leiomyoma of the corpus uteri and vulva.
The paper describes a case of multiple uterine leiomyomas concurrent with vulvar leiomyoma in a 39-year-old patient with progressive tumor nodule growth over 2 years. Vulvar tumor was biopsied simultaneously with extirpation of the uterus; vulvar leiomyoma was removed six months later. Histological and immunohistochemical studies: such as hematoxylin and eosin staining, the expression of smooth muscle actin, desmin, and progesterone and estrogen receptors, S100, CD10, and determination of Ki-67 proliferation index, were conducted.
The largest (14-cm) multiple tumor nodule in the corpus uteri had the structure of leiomyoma of uncertain malignant potential; the large (8-cm) vulvar tumor was a leiomyoma with hyalinosis. The immunohistochemical profile of uterine and vulvar leiomyoma (smooth muscle actin+, desmin+, progesterone+, estrogen+ receptors, CD117-, and Ki-67) was the same (1-3%). The vulvar leiomyoma was assumed to be a tumor of metastatic origin.
Vulvar leiomyoma is rare; it can arise from smooth muscle tissue of various anatomical structures of the skin and soft tissues. The pathogenesis of the so-called metastatic leiomyoma is unclear; there are concepts of a metaplastic transformation of subcelomic mesenchyme and multifocal smooth muscle proliferation. The presented case demonstrates the synchronous development of uterine and vulvar leiomyoma.
揭示同时诊断出的子宫体平滑肌瘤和外阴平滑肌瘤的形态学特征。
本文描述了一例39岁患者,患有多发性子宫平滑肌瘤并伴有外阴平滑肌瘤,肿瘤结节在2年中逐渐增大。在外阴肿瘤切除子宫的同时进行活检;6个月后切除外阴平滑肌瘤。进行了组织学和免疫组织化学研究:如苏木精和伊红染色、平滑肌肌动蛋白、结蛋白、孕激素和雌激素受体的表达、S100、CD10以及Ki-67增殖指数的测定。
子宫体最大的(14厘米)多发性肿瘤结节具有恶性潜能不确定的平滑肌瘤结构;较大的(8厘米)外阴肿瘤是伴有透明变性的平滑肌瘤。子宫和外阴平滑肌瘤的免疫组织化学特征(平滑肌肌动蛋白阳性、结蛋白阳性、孕激素阳性、雌激素受体阳性、CD117阴性、Ki-67)相同(1%-3%)。外阴平滑肌瘤被认为是转移性肿瘤。
外阴平滑肌瘤罕见;它可起源于皮肤和软组织各种解剖结构的平滑肌组织。所谓转移性平滑肌瘤的发病机制尚不清楚;存在间皮间充质化生和多灶性平滑肌增殖的概念。本病例展示了子宫和外阴平滑肌瘤的同步发展。