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一例极为罕见的恶性腺瘤合并巨大囊性肿瘤导致尿路梗阻的病例。

An extremely rare case of adenoma malignum with large cystic tumor which resulted in urinary obstruction.

作者信息

Gotoh Tomoko, Kikuchi Yoshihiro, Takano Masashi, Kita Tsunekazu, Ogata Sho, Aida Shinsuke, Anzai Mikio

机构信息

Department of Obstetrics and Gynecology, National Defense Medical College, Namiki 3-2, Tokorozawa, Saitama 359-8513, Japan.

出版信息

Gynecol Oncol. 2002 Feb;84(2):339-43. doi: 10.1006/gyno.2001.6530.

Abstract

BACKGROUND

Adenoma malignum is a rare variant of uterine cervical adenocarcinoma. In this report, we present an extremely rare case of adenoma malignum with large cystic lesions (diameter of more than 10 cm) which elicited urinary obstruction.

CASE

A 46-year-old Japanese woman, gravida 2, para 2, visited her local doctor for urinary obstruction, and 950 ml of urine was catheterized. Since abdominal ultrasonography suggested ovarian cystic tumor, she was referred to our hospital. Vaginal examination and ultrasonography revealed a child-head-sized multilocular cystic tumor in the Douglas pouch. Abnormal massive discharge was not observed at the time of admission. During preoperative examination, massive mucinous discharge suddenly occurred without pain. The cystic tumor size shrank from x10 cm to x4.0 cm in maximum diameter. Emergent abdominal hysterectomy was performed. The operative findings revealed collapsed cystic lesions in the posterior wall of the uterine cervix. Microscopically, the multiple cysts in the cervix were composed of high columnar and slightly atypical monolayer cells similar to endocervical mucinous cells. Vaginal invasion was also partly observed. Most of the tumor cells were positive for carcinoembryonic antigen and HIK1083 in their cytoplasm, and scattered chromogranin A-positive endocrine cells were also found in tumor glands, corresponding to minimal deviation adenocarcinoma (adenoma malignum). These lesions were diagnosed as FIGO stage IIa. The patient is disease-free 2 years after primary surgery.

CONCLUSION

In the present report, we describe an extremely rare case of adenoma malignum with large cystic lesions reaching a diameter of 12 cm which resulted in urinary obstruction.

摘要

背景

恶性腺瘤是子宫颈腺癌的一种罕见变异型。在本报告中,我们呈现了一例极其罕见的伴有大囊性病变(直径超过10厘米)并引发尿路梗阻的恶性腺瘤病例。

病例

一名46岁的日本女性,孕2产2,因尿路梗阻前往当地医生处就诊,导尿950毫升。由于腹部超声提示卵巢囊性肿瘤,她被转诊至我院。阴道检查和超声显示Douglas窝有一个儿童头大小的多房囊性肿瘤。入院时未观察到异常大量分泌物。在术前检查期间,突然无痛出现大量黏液性分泌物。囊性肿瘤大小最大直径从10厘米缩小至4.0厘米。急诊行腹式子宫切除术。手术所见显示子宫颈后壁有塌陷的囊性病变。显微镜下,宫颈的多个囊肿由高柱状且略有异型的单层细胞组成,类似于宫颈黏液细胞。还部分观察到阴道浸润。大多数肿瘤细胞胞质内癌胚抗原和HIK1083呈阳性,在肿瘤腺体内还发现散在的嗜铬粒蛋白A阳性内分泌细胞,符合微偏腺癌(恶性腺瘤)。这些病变被诊断为国际妇产科联盟(FIGO)IIa期。患者在初次手术后2年无疾病复发。

结论

在本报告中,我们描述了一例极其罕见的恶性腺瘤病例,其大囊性病变直径达12厘米,导致尿路梗阻。

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