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CASE REPORT article

Front. Oncol.

Sec. Thoracic Oncology

This article is part of the Research TopicMechanisms Linking Cancer and Metabolic Diseases: From Molecular Pathways to Therapeutic InterventionsView all 4 articles

Intraoperative Vascular Ligation Uncovers the Role of Tumor Vasculature in Doege-Potter Syndrome: A Case Report

Provisionally accepted
Lin  DuLin DuKai  WeiKai WeiNa  LiNa LiYajing  SunYajing SunDongmei  LiuDongmei LiuGeng  XuGeng XuTao  YangTao YangXiuqiang  ZhangXiuqiang Zhang*
  • Tianjin Fifth Center Hospital, Tianjin, China

The final, formatted version of the article will be published soon.

Solitary fibrous tumor (SFT) is a rare mesenchymal neoplasm that may present with non-islet cell tumor hypoglycemia (NICTH), also referred to as Doege-Potter syndrome, primarily due to aberrant secretion of big-IGF2. However, not all big-IGF2-producing SFTs result in hypoglycemia, implying the involvement of additional pathogenic factors. This article reports a case of a 60-year-old male who presented with hypoglycemic syncope secondary to Doege-Potter syndrome. Preoperative imaging identified a large, highly vascularized SFT, approximately 20 cm in diameter, located in the right thoracic cavity. Intraoperative continuous glucose monitoring (CGM) recorded a gradual normalization of blood glucose levels following sequential ligation of three dominant tumor vessels originated from veins-prior to tumor resection - underscoring the essential role of tumor vascular in facilitating big-IGF2 release. Our findings provide the first direct evidence that tumor vasculature is critical for manifesting clinically significant hypoglycemia, thereby complementing established molecular mechanisms such as IGF2 overexpression and impaired pro-IGF2 processing. These insights advance the understanding of NICTH pathogenesis and hold meaningful implications for refining surgical management strategies.

Keywords: Big-IGF2, Doege-Potter syndrome, Non-islet cell tumor hypoglycemia, Solitaryfibrous tumor, vascular

Received: 25 Sep 2025; Accepted: 13 Feb 2026.

Copyright: © 2026 Du, Wei, Li, Sun, Liu, Xu, Yang and Zhang. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Xiuqiang Zhang

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