Primary hepatic angiosarcoma mistaken for a giant hemangioma.

IF 1.6 Q2 MEDICINE, GENERAL & INTERNAL Intractable & rare diseases research Pub Date : 2025-02-28 DOI:10.5582/irdr.2024.01045
Xu Jing Qian, Safwat Girgis, Mitchell P Wilson, Gavin Low
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引用次数: 0

Abstract

Primary hepatic angiosarcoma (PHA) is a rare hepatic mesenchymal tumor that accounts for 2% of all primary malignant liver tumors. It typically presents with nonspecific symptoms, is highly aggressive, and there are limited treatment options. Imaging characteristics of PHA overlap with that of hepatic hemangioma, a common benign hepatic lesion, creating a potential diagnostic pitfall. We present a case of PHA that mimicked hepatic hemangioma on imaging. We review the differentiating characteristics between these two hepatic tumors. PHAs demonstrate irregular/infiltrating margins, higher lesion multiplicity, higher risk of tumor rupture, and rapid growth, which are not typically seen with hepatic hemangiomas.

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原发性肝血管肉瘤被误认为巨大的血管瘤。
原发性肝血管肉瘤(PHA)是一种罕见的肝脏间质肿瘤,占所有原发性恶性肝脏肿瘤的2%。它通常表现为非特异性症状,具有高度侵袭性,治疗方案有限。肝血管瘤是一种常见的良性肝脏病变,PHA的影像学特征与肝血管瘤重叠,从而造成潜在的诊断缺陷。我们报告一例PHA在影像学上模仿肝血管瘤。我们回顾这两种肝肿瘤的鉴别特征。pha表现为不规则/浸润性边缘,病变多样性高,肿瘤破裂风险高,生长迅速,这些在肝血管瘤中并不常见。
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来源期刊
Intractable & rare diseases research
Intractable & rare diseases research MEDICINE, GENERAL & INTERNAL-
CiteScore
2.10
自引率
0.00%
发文量
29
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