伪装为肝脓肿的原发性肝平滑肌肉瘤1例。

IF 1.8 4区 医学 Q3 GASTROENTEROLOGY & HEPATOLOGY
Fang-Nan Wu, Min Zhang, Kun Zhang, Xin-Liang Lv, Jing-Qiang Guo, Chao-Yong Tu, Qing-Yun Zhou
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引用次数: 0

摘要

背景:原发性肝纤维肉瘤(PHL)是一种罕见的恶性肿瘤,其临床表现和影像学特征均无特异性,因此术前诊断具有挑战性。病例摘要:患者为一名 34 岁女性,入院前 4 天出现右上腹痛和发热。根据患者的病史、实验室检查和影像学检查,怀疑是肝脓肿。经皮肝穿刺活检确诊为间质瘤,并进行了肝部分切除术。术后病理结果显示为 PHL。患者目前正在接受 AD 方案静脉化疗,没有复发迹象:结论:当肝脏病变壁厚、血供丰富,并伴有大量不均匀的低密度区时,应考虑 PHL。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Primary hepatic leiomyosarcoma masquerading as liver abscess: A case report.

Background: Primary hepatic leiomyosarcoma (PHL) is a rare malignant tumor and has non-specific clinical manifestations and imaging characteristics, making preoperative diagnosis challenging. Here, we report a case of PHL presenting primarily with fever, with computed tomography imaging showing a thick-walled hepatic lesion with low-density areas, resembling liver abscess.

Case summary: The patient was a 34-year-old woman who presented with right upper abdominal pain and fever over 4 days before admission. Based on the patient's medical history, laboratory examinations, and imaging examinations, liver abscess was suspected. Mesenchymal tumor was diagnosed by percutaneous liverbiopsy and partial hepatectomy was performed. Postoperative pathology revealed PHL. The patient is currently undergoing intravenous chemotherapy with the AD regimen and shows no signs of recurrence.

Conclusion: When there is a thick wall and rich blood supply in the hepatic lesion with a large proportion of uneven low-density areas, PHL should be considered.

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