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原发性淋巴结胃泌素瘤伴肝转移导致卓-艾综合征的治疗。

Management of Primary Lymph Nodal Gastrinoma With Liver Metastases Resulting in Zollinger-Ellison Syndrome.

机构信息

From the Departments of Nuclear Medicine.

Gastroentrology.

出版信息

Clin Nucl Med. 2019 Jan;44(1):e36-e39. doi: 10.1097/RLU.0000000000002368.

Abstract

Primary lymph node gastrinoma has been defined as gastrin-producing tumor present in lymph nodes and predominantly found in well-defined anatomical region known as gastrinoma triangle. They are usually localized preoperatively with imaging, and their surgical resection results in long-term relief. The authors report a case of unresectable primary lymph nodal gastrinoma with liver metastases in a 14-year-old adolescent boy with proven histopathology detected on Ga-DOTANOC whole-body PET/CT scan followed by preoperative multiple Lu-DOTATATE cycles for cytoreduction. Subsequent surgical resection of residual mass resulted in complete response with a follow-up of around 4 years in this unusual case of Zollinger-Ellison syndrome.

摘要

原发性淋巴结胃泌素瘤被定义为存在于淋巴结中的胃泌素产生肿瘤,主要位于称为胃泌素瘤三角的明确解剖区域。它们通常可以通过影像学在术前定位,并且手术切除可获得长期缓解。作者报告了一例 14 岁青少年患有不可切除的原发性淋巴结胃泌素瘤伴肝转移的病例,该病例通过 Ga-DOTANOC 全身 PET/CT 扫描证实了组织病理学,并随后进行了多次 Lu-DOTATATE 术前周期以进行细胞减灭术。在这种不寻常的 Zollinger-Ellison 综合征病例中,残余肿瘤的后续手术切除导致完全缓解,随访约 4 年。

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