[Doege-Potter syndrome and intra-abdominal giant solitary fibrous tumor: Case report].

Antonio Lira-Díaz, Daniel Arizpe-Vilana, María Guadalupe Jazmín de Anda-González
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Abstract

Background: Doege-Potter syndrome has been reported in solitary fibrous tumors and it is characterized by severe, sustained, and refractory hypoglycemia associated with non-pancreatic tumors, particularly solitary fibrous tumor of the pleura. An uncommon case of solitary fibrous tumor associated with severe hypoglycemia and abdominal location is reported.

Clinical case: A 63-year-old woman presented with difficult-to-control hypoglycemia, intestinal obstruction, and subsequent sepsis. Imaging studies showed an abdominal-predominant neoplasm infiltrating the spine. Histopathological examination of the biopsy and surgical specimen confirmed a solitary fibrous tumor. Once resected, the hypoglycemia diminished and Doege-Potter syndrome was diagnosed.

Conclusion: This case stands out due to its presentation with severe refractory hypoglycemia, the location of the tumor in the abdomen, and vertebral invasion, given that most solitary fibrous tumors are found in the lungs and originate from the pleura. Uncommon causes of hypoglycemia in non-diabetic patients should be considered, such as Doege-Potter syndrome.

[doge - potter综合征合并腹腔内巨大孤立性纤维性肿瘤1例]。
背景:Doege-Potter综合征在孤立性纤维性肿瘤中已有报道,其特征是与非胰腺肿瘤,特别是胸膜孤立性纤维性肿瘤相关的严重、持续和难治性低血糖。本文报告一例罕见的孤立性纤维性肿瘤伴严重低血糖及腹部病变。临床病例:一名63岁女性,表现为难以控制的低血糖,肠梗阻,随后脓毒症。影像学检查显示以腹部为主的肿瘤浸润脊柱。组织病理学检查活检和手术标本证实一个孤立的纤维性肿瘤。一旦切除,低血糖降低,诊断为多吉-波特综合征。结论:该病例表现为严重难治性低血糖,肿瘤位于腹部,并侵犯椎体,因为大多数孤立的纤维性肿瘤见于肺部并起源于胸膜。非糖尿病患者低血糖的不常见原因应考虑,如多吉-波特综合征。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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