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子宫内膜癌脾转移 1 例报告并文献复习

Splenic metastasis from endometrial carcinoma: report of a case and review of literature.

机构信息

Department of Obstetrics and Gynecology, Soroka Medical Center, Ben-Gurion University of the Negev, Beersheba, Israel.

出版信息

Arch Gynecol Obstet. 2009 Dec;280(6):1001-6. doi: 10.1007/s00404-009-1039-7. Epub 2009 Mar 21.

Abstract

INTRODUCTION

Splenic metastasis from endometrial carcinoma is a rare clinical event, with only 11 cases documented previously in the literature.

CASE REPORT

A 58-year-old woman had surgery and radiotherapy for stage IIB endometrial carcinoma. Eighteen months later, PET scan discovered a hypermetabolic splenic mass and two hypermetabolic lung nodules. Spleen biopsy showed metastasis from endometrial carcinoma. Chemotherapy with six cycles of cyclophosphamide, adriamycin and cisplatin effected a partial response of the splenic and lung metastasis. After few months, however, splenectomy was performed because of substantial growth of the spelnic metastasis and it confirmed that the splenic metastasis was of endometrial origin and solitary in the peritoneal cavity. After splenectomy, the patient received chemotherapy with six cycles of paclitaxel. To date, 6 months after splenectomy, she is alive with no intraperitoneal disease and with few stable lung metastases.

CONCLUSION

This is the 12th reported case of splenic metastasis from endometrial carcinoma. Splenic metastasis from endometrial carcinoma is usually solitary splenic metastasis limited to the splenic parenchyma. Splenectomy is an appropriate treatment to avoid splenic rupture, splenic vein thrombosis and painful splenomegaly, to circumvent the splenic metastasis being a source of secondary metastatic disease, and to provide the potential for cure or extended survival. Since patients with splenic metastasis may be asymptomatic and the interval between the diagnoses of endometrial carcinoma and splenic metastasis may be prolonged, careful and extended follow-up after primary treatment of endometrial carcinoma is warranted.

摘要

简介

脾转移来自子宫内膜癌是一种罕见的临床事件,文献中此前仅记录了 11 例。

病例报告

一名 58 岁女性因 IIB 期子宫内膜癌接受了手术和放疗。18 个月后,PET 扫描发现脾脏有高代谢性肿块和两个高代谢性肺结节。脾活检显示为子宫内膜癌转移。接受 6 个周期环磷酰胺、阿霉素和顺铂化疗后,脾和肺转移的部分反应。然而,几个月后,由于脾转移的大量生长,进行了脾切除术,证实脾转移来自子宫内膜癌且在腹膜腔内为单发。脾切除术后,患者接受了 6 个周期紫杉醇化疗。截至目前,脾切除术后 6 个月,患者无腹腔内疾病且肺部转移灶稳定。

结论

这是第 12 例报道的来自子宫内膜癌的脾转移病例。来自子宫内膜癌的脾转移通常为单发局限于脾脏实质的脾转移。脾切除术是一种合适的治疗方法,可避免脾破裂、脾静脉血栓形成和疼痛性脾肿大,避免脾转移成为继发性转移疾病的来源,并为治愈或延长生存提供可能。由于脾转移患者可能无症状且子宫内膜癌和脾转移之间的间隔时间可能延长,因此有必要在子宫内膜癌的初始治疗后进行仔细和延长的随访。

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