Podczaski E, Kaminski P F, Pees R C, Singapuri K, Sorosky J I
Department of Obstetrics & Gynecology, M. S. Hershey Medical Center, Pennsylvania State University, Hershey 17033.
Gynecol Oncol. 1991 Jul;42(1):74-8. doi: 10.1016/0090-8258(91)90234-v.
A patient with Peutz-Jeghers syndrome, a sex cord tumor with annular tubules, and an initially unrecognized adenoma malignum of the cervix is described. The patient presented with a mucinous adenocarcinoma in the vaginal apex. Review of the hysterectomy slides demonstrated an adenoma malignum of the cervix. In addition to a microscopic sex cord tumor with annular tubules of the right ovary, the left ovary contained mucinous cystadenomas. Adenoma malignum remains a difficult diagnosis and is frequently made only after hysterectomy for a presumed benign indication; pathology frequently demonstrates a deeply invasive, unusually well-differentiated adenocarcinoma of the cervix. Patients with Peutz-Jeghers syndrome need careful clinical and cytologic follow-up to exclude such lesions.
本文描述了一名患有黑斑息肉综合征、环形小管性索肿瘤以及最初未被识别的宫颈恶性腺瘤的患者。该患者阴道顶端出现黏液性腺癌。对子宫切除术后的切片进行复查发现了宫颈恶性腺瘤。除右侧卵巢有一个显微镜下可见的环形小管性索肿瘤外,左侧卵巢还含有黏液性囊腺瘤。宫颈恶性腺瘤仍然是一个难以诊断的疾病,通常仅在因假定为良性指征而进行子宫切除术后才能确诊;病理检查常常显示为宫颈的一种深度浸润、分化异常良好的腺癌。黑斑息肉综合征患者需要进行仔细的临床和细胞学随访以排除此类病变。