Spatz A, Bouron D, Pautier P, Castaigne D, Duvillard P
Department of Pathology, Institut Gustave-Roussy, Villejuif, 94805, France.
Gynecol Oncol. 1998 Aug;70(2):285-8. doi: 10.1006/gyno.1998.5036.
A 49-year-old woman was admitted with abnormal vaginal bleeding of 5 months duration. Hysteroscopy showed polypoid formations in the uterine cavity. Biopsy of a polyp revealed an anaplastic malignant tumor. A total hysterectomy with bilateral salpingo-oophorectomy and iliac lymphadenectomy were performed. A polypoid soft white-yellowish tumor originated from the endometrium. The biopsies plus sections of the operative specimen were histologically similar and displayed typical features of yolk sac tumor (YST) with tubulo-papillary pattern. Schiller-Duval bodies and PAS-positive, diastase-resistant, hyaline droplets were present. There was no neoplastic involvement of the cervix, ovaries, and iliac lymph nodes. Tumor cells and hyaline globules were strongly immunoreactive with alpha-fetoprotein antibody. The patient refused chemotherapy and was subsequently treated by external radiotherapy. The patient remained free of disease 28 months after surgery. There are only four additional cases of primary YST of the endometrium reported in literature. On the basis of the small number of cases reported, such tumors appear to have clinical and pathological features similar to their ovarian counterparts.
一名49岁女性因持续5个月的异常阴道出血入院。宫腔镜检查显示宫腔内有息肉样肿物。对一个息肉进行活检,结果显示为间变性恶性肿瘤。遂行全子宫切除术、双侧输卵管卵巢切除术及髂淋巴结清扫术。一个息肉样的软质黄白色肿瘤起源于子宫内膜。手术标本的活检及切片在组织学上相似,呈现出卵黄囊瘤(YST)典型的小管乳头状结构特征。可见席勒-杜瓦尔小体以及PAS阳性、抗淀粉酶、透明样小滴。宫颈、卵巢及髂淋巴结均无肿瘤累及。肿瘤细胞及透明样小球对甲胎蛋白抗体呈强免疫反应性。患者拒绝化疗,随后接受了体外放疗。术后28个月患者无疾病复发。文献中仅另外报道了4例原发性子宫内膜YST病例。基于所报道的病例数量较少,此类肿瘤似乎具有与其卵巢同类肿瘤相似的临床和病理特征。