A case report: Masson's tumor (intravascular papillary endothelial hyperplasia) of the abdominal cavity.

IF 2 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY Journal of gastrointestinal oncology Pub Date : 2026-02-28 Epub Date: 2026-01-16 DOI:10.21037/jgo-2025-635
Yiran Ren, Xiangrong Yu
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Abstract

Background: Masson's tumor, also known as intravascular papillary endothelial hyperplasia (IPEH), is a rare benign vascular lesion that can arise in a wide range of anatomical sites, most frequently within the dermis and subcutaneous tissues. Because its clinical manifestations and radiological appearances are nonspecific and may closely mimic those of malignant vascular neoplasms or soft-tissue sarcomas, it is frequently misinterpreted as a malignant tumor, particularly in the preoperative setting. To draw attention to this important diagnostic pitfall, we present a case of IPEH that was initially misdiagnosed as a malignant lesion, with the aim of improving recognition of its characteristic features and thereby enhancing diagnostic accuracy and reducing the likelihood of future misdiagnosis.

Case description: A 52-year-old woman was incidentally found to have a well-circumscribed, hypervascular intra-abdominal mass during a chest computed tomography (CT) scan. Magnetic resonance imaging showed a T1-hypointense/T2-hyperintense lesion with restricted diffusion and progressive enhancement. Given its marked hypervascularity and intra-abdominal location, a neoplastic process was initially suspected. However, following surgical exploration with complete excision of the mass and histopathological evaluation, the lesion was ultimately diagnosed as IPEH.

Conclusions: Intra-abdominal Masson's tumor is exceedingly rare, and its imaging characteristics have not been systematically defined. In this report, we describe a surgically confirmed case of intra-abdominal Masson's tumor and place particular emphasis on its radiological features, including a well-circumscribed hyper vascular mass with progressive enhancement but without overt signs of malignancy. Despite these suggestive imaging findings, the definitive diagnosis continues to depend on histopathological assessment combined with immunohistochemical staining. By presenting this case, we hope to raise awareness of this benign yet deceptive vascular lesion and highlight that a pattern of progressive enhancement in the absence of malignant imaging features may prompt consideration of Masson's tumor in the differential diagnosis, thereby facilitating earlier and more accurate diagnosis.

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腹腔马松瘤(血管内乳头状内皮增生)1例报告。
背景:马松肿瘤,也被称为血管内乳头状内皮增生(IPEH),是一种罕见的良性血管病变,可发生在广泛的解剖部位,最常见于真皮和皮下组织。由于其临床表现和影像学表现是非特异性的,可能与恶性血管肿瘤或软组织肉瘤非常相似,因此经常被误认为是恶性肿瘤,尤其是在术前。为了引起人们对这一重要诊断缺陷的注意,我们报告了一例最初被误诊为恶性病变的IPEH,目的是提高对其特征的认识,从而提高诊断准确性,减少未来误诊的可能性。病例描述:一名52岁女性在胸部计算机断层扫描(CT)时偶然发现有一个界限清楚的高血管腹内肿块。磁共振成像显示t1 -低信号/ t2 -高信号病变,扩散受限,进行性增强。鉴于其明显的血管扩张和腹腔内的位置,最初怀疑是肿瘤过程。然而,经过手术探查,完全切除肿块和组织病理学评估,病变最终被诊断为IPEH。结论:腹内马松肿瘤极为罕见,其影像学特征尚未系统界定。在本报告中,我们描述了一例手术确诊的腹内马松肿瘤,并特别强调了其放射学特征,包括一个界限明确的高血管肿块,呈进行性增强,但没有明显的恶性肿瘤迹象。尽管有这些暗示性的影像学发现,最终的诊断仍然依赖于组织病理学评估和免疫组织化学染色。通过这个病例,我们希望提高人们对这种良性但具有欺骗性的血管病变的认识,并强调在没有恶性影像学特征的情况下,渐进式增强的模式可能会促使在鉴别诊断中考虑Masson肿瘤,从而促进早期和更准确的诊断。
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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
171
期刊介绍: ournal of Gastrointestinal Oncology (Print ISSN 2078-6891; Online ISSN 2219-679X; J Gastrointest Oncol; JGO), the official journal of Society for Gastrointestinal Oncology (SGO), is an open-access, international peer-reviewed journal. It is published quarterly (Sep. 2010- Dec. 2013), bimonthly (Feb. 2014 -) and openly distributed worldwide. JGO publishes manuscripts that focus on updated and practical information about diagnosis, prevention and clinical investigations of gastrointestinal cancer treatment. Specific areas of interest include, but not limited to, multimodality therapy, markers, imaging and tumor biology.
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