Clement P B, Scully R E
Department of Pathology, Vancouver General Hospital, Canada.
Int J Gynecol Pathol. 1992 Jul;11(3):163-73.
Three cases of endometrial stromal sarcoma (ESS) with prominent glandular differentiation within the primary or recurrent tumors are described. Each case posed a problem in diagnosis and classification. The patients, who ranged in age from 41 to 47 years, presented with abnormal uterine bleeding, a pelvic mass, or a combination thereof. All the patients underwent hysterectomy with or without bilateral salpingo-oophorectomy. There was no evidence of extrauterine spread of tumor in any case. Polypoid tumors involved the endometrium in two cases, and in one of them, tumor deeply invaded the myometrium. The tumor in the third case was an infiltrative mass that was confined to the myometrium and its vessels. On microscopic examination, the tumors were low-grade ESSs that contained large numbers of endometrioid glands, which were benign appearing in two cases, and in the third varied from atypical to carcinomatous. In one of the cases in the first group, the glandular component was present only in recurrent tumor excised 10 years after hysterectomy; prominent foci of sex-cord-like differentiation were also present in the recurrent tumor. This patient was clinically free of tumor 27 months later; follow-up in the other two patients was uneventful. ESSs with prominent numbers of benign-appearing glands should be distinguished from adenomyosis, endometriosis, ESSs arising in adenomyosis or endometriosis, ESSs with sex-cord-like differentiation, and müllerian adenosarcomas. ESSs with carcinomatous glands should be distinguished from endometrial adenocarcinomas and malignant müllerian mixed tumors (carcinosarcomas). Extrauterine lesions that have been designated "aggressive endometriosis" may be examples of extrauterine ESS with prominent glandular differentiation.
本文描述了3例原发性或复发性肿瘤内具有显著腺体分化的子宫内膜间质肉瘤(ESS)。每例病例在诊断和分类方面都存在问题。患者年龄在41至47岁之间,表现为子宫异常出血、盆腔肿块或两者兼有。所有患者均接受了子宫切除术,部分患者还接受了双侧输卵管卵巢切除术。所有病例均无肿瘤宫外转移的证据。2例息肉样肿瘤累及子宫内膜,其中1例肿瘤深度浸润肌层。第3例肿瘤为浸润性肿块,局限于肌层及其血管。显微镜检查显示,这些肿瘤为低级别ESS,含有大量子宫内膜样腺体,其中2例腺体外观良性,第3例则从非典型到癌性不等。在第一组的1例病例中,腺体成分仅存在于子宫切除术后10年切除的复发性肿瘤中;复发性肿瘤中也存在显著的性索样分化灶。该患者在27个月后临床无肿瘤;另外2例患者的随访情况良好。具有大量外观良性腺体的ESS应与子宫腺肌病、子宫内膜异位症、起源于子宫腺肌病或子宫内膜异位症的ESS、具有性索样分化的ESS以及苗勒管腺肉瘤相鉴别。具有癌性腺体的ESS应与子宫内膜腺癌和恶性苗勒管混合瘤(癌肉瘤)相鉴别。被称为“侵袭性子宫内膜异位症”的宫外病变可能是具有显著腺体分化的宫外ESS的例子。