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行保留胰腺的节段性十二指肠切除术治疗十二指肠胃肠道间质瘤,行脾切除术治疗脾血管肉瘤。

Pancreas-preserving segmental duodenectomy for gastrointestinal stromal tumor of the duodenum and splenectomy for splenic angiosarcoma.

机构信息

Department of General Surgery, La Sapienza University of Rome, Rome, Italy.

出版信息

Hepatobiliary Pancreat Dis Int. 2012 Jun;11(3):325-9. doi: 10.1016/s1499-3872(12)60169-6.

Abstract

BACKGROUND

Gastrointestinal stromal tumors are the most common mesenchymal tumors of the gastrointestinal tract and occur rarely in the duodenum. Splenic angiosarcoma is an aggressive neoplasm with an extremely poor prognosis.

METHODS

We report a case of a 70-year-old man hospitalized for abdominal pain in the upper quadrants, dyspepsia and nausea, previously treated for Hodgkin lymphoma 30 years ago. Abdominal CT showed a solid nodular lesion in the third portion of the duodenum, the presence of retropancreatic, aortic and caval lymph nodes, and four nodular splenic masses. (111)In-octreotide scintigraphy revealed pathological tissue accumulation in the duodenal region, and in the retropancreatic, retroduodenal, aortic and caval lymph nodes, suggesting a nonfunctioning neuroendocrine peripancreatic tumor.

RESULTS

At exploratory laparotomy, an exophytic soft tumor was found originating from the third portion of the duodenum. Pancreas-preserving duodenectomy with duodenojejunostomy, splenectomy and lymphnodectomy of retropancreatic aortic and caval lymph nodes were performed. Pathological evaluation and immunohistochemical studies showed the presence of a duodenal gastrointestinal stromal tumor with low mitotic activity and a well-differentiated angiosarcoma localized to the spleen and invading lymph nodes.

CONCLUSIONS

We speculated that the angiosarcoma and duodenal gastrointestinal stromal tumors of this patient were due to the treatment of Hodgkin lymphoma with radiotherapy 30 years ago. Pancreas-preserving segmental duodenectomy can be used to treat non-malignant neoplasms of the duodenum and avoid extensive surgery. Splenectomy is the treatment of choice for localized angiosarcomas but a strict follow-up is mandatory because of the possibility of recurrence.

摘要

背景

胃肠道间质瘤是胃肠道最常见的间叶性肿瘤,在十二指肠中很少见。脾血管肉瘤是一种侵袭性肿瘤,预后极差。

方法

我们报告了一例 70 岁男性患者,因上腹部疼痛、消化不良和恶心住院,30 年前曾接受霍奇金淋巴瘤治疗。腹部 CT 显示十二指肠第三部分有一个实性结节状病变,胰后、主动脉和腔静脉淋巴结存在,还有四个结节状脾肿块。(111)In-奥曲肽闪烁显像显示十二指肠区域、胰后、十二指肠后、主动脉和腔静脉淋巴结存在病理性组织积聚,提示为无功能胰腺周围神经内分泌肿瘤。

结果

在剖腹探查时,发现一个来源于十二指肠第三部分的外生软肿瘤。行保留胰腺的十二指肠切除术,行十二指肠空肠吻合术、脾切除术和胰后、主动脉和腔静脉淋巴结切除术。病理评估和免疫组织化学研究显示,存在低有丝分裂活性的十二指肠胃肠道间质瘤和局限于脾脏和侵犯淋巴结的分化良好的血管肉瘤。

结论

我们推测该患者的血管肉瘤和十二指肠胃肠道间质瘤是由于 30 年前接受霍奇金淋巴瘤放射治疗所致。保留胰腺的节段性十二指肠切除术可用于治疗十二指肠非恶性肿瘤,并避免广泛手术。脾切除术是局限性血管肉瘤的治疗选择,但由于有复发的可能,需要严格随访。

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