Suppr超能文献

转移性绒毛膜癌作为无原发性子宫病变时小肠穿孔的首发表现:一例报告

Metastatic choriocarcinoma as initial presentation of small bowel perforation in absence of primary uterine lesion: a case report.

作者信息

Cho En Bee, Byun Jung Mi, Jeong Dae Hoon, Yoon Hye Kyoung, Kim Young Nam, Sung Moon Su, Lee Kyung Bok, Kim Ki Tae

机构信息

Department of Obstetrics and Gynecology, Busan Paik Hospital, Inje University, Busan - Korea.

Paik Institute for Clinical Research, Busan Paik Hospital, Inje University, Busan - Korea.

出版信息

Tumori. 2016 Nov 11;102(Suppl. 2):D07579C9-2D29-4270-B169-20841C554FB7. doi: 10.5301/tj.5000379.

Abstract

BACKGROUND

Choriocarcinoma is a highly malignant tumor of gestational trophoblastic neoplasia that characteristically spreads via the bloodstream. Small bowel metastasis is very rare, and a small number of cases of choriocarcinoma metastasis to small bowel have been reported.

METHODS

We report a case of a 40-year-old woman presenting with acute abdominal pain and vaginal bleeding due to small bowel perforation secondary to jejunal metastasis. In our case, metastatic choriocarcinoma was present in the small bowel, lung, and liver, but no primary lesion was apparent.

RESULTS

After resection and anastomosis of the perforated small bowel, chemotherapy was performed. The patient began chemotherapy with etoposide, methotrexate, actinomycin D, cyclophosphamide, and vincristine (EMA-CO) for 9 cycles. When the 4th cycle of chemotherapy was finished, β-human chorionic gonadotropin (hCG) level was normalized and follow-up computed tomography scans showed regression of the liver metastasis and small bowel lesion and significantly decreased lung metastasis. After 9 cycles of chemotherapy were completed, the patient showed complete response.

CONCLUSIONS

If patients have high β-hCG of unknown origin and suspected panperitonitis, which are suspicious of choriocarcinoma metastasis to small bowel, the pathologic findings are important. It is essential to confirm the histopathologic diagnosis postoperatively. Choriocarcinoma can spread to various organs and show aggressive manifestations. Therefore, we should be aware of possible metastatic sites and remain alert to its diagnosis.

摘要

背景

绒毛膜癌是妊娠滋养细胞肿瘤中一种高度恶性的肿瘤,其特征是通过血液扩散。小肠转移非常罕见,仅有少数绒毛膜癌转移至小肠的病例报道。

方法

我们报告一例40岁女性患者,因空肠转移继发小肠穿孔出现急性腹痛和阴道出血。在我们的病例中,小肠、肺和肝脏均存在转移性绒毛膜癌,但未发现明显的原发灶。

结果

对穿孔的小肠进行切除和吻合后,进行了化疗。患者开始使用依托泊苷、甲氨蝶呤、放线菌素D、环磷酰胺和长春新碱(EMA-CO)进行化疗,共9个周期。在化疗第4个周期结束时,β-人绒毛膜促性腺激素(hCG)水平恢复正常,后续的计算机断层扫描显示肝转移和小肠病变消退,肺转移明显减少。完成9个周期的化疗后,患者显示完全缓解。

结论

如果患者β-hCG升高且来源不明,同时怀疑有弥漫性腹膜炎,怀疑绒毛膜癌转移至小肠,病理结果很重要。术后确认组织病理学诊断至关重要。绒毛膜癌可扩散至各个器官并表现出侵袭性。因此,我们应了解可能的转移部位,并对其诊断保持警惕。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验