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肝脏低度恶性肌纤维母细胞肉瘤误诊为囊腺瘤:一例报告。

Low-grade myofibroblastic sarcoma of the liver misdiagnosed as cystadenoma: A case report.

机构信息

Department of Ultrasonic Imaging, Xiangya Hospital, Central South University, Changsha 410008, Hunan Province, China.

出版信息

World J Gastroenterol. 2022 Aug 21;28(31):4456-4462. doi: 10.3748/wjg.v28.i31.4456.

Abstract

BACKGROUND

Low-grade myofibroblastic sarcoma (LGMS) is a rare malignant tumor. It has no specific clinical manifestations and commonly occurs in the head and neck, extremities and other body parts, with the liver not as its predisposing site.

CASE SUMMARY

We report a case report of a 58-year-old man with right upper abdominal pain for 11 d. Contrast-enhanced computed tomography (CECT), CE magnetic resonance imaging and CE ultrasound (US) all showed a cystic-solid mass in the right liver. As the initial clinical diagnosis was hepatic cystadenoma, surgical resection was performed, and the postoperative pathology indicated hepatic LGMS. The 3-mo follow-up showed favorable recovery of the patient. However, at 7-mo follow-up, two-dimensional US and CECT showed a suspected metastatic lesion in the right-middle abdomen.

CONCLUSION

Hepatic MS is particularly rare and easily misdiagnosed, more cases will contribute to the understanding and the diagnosis accuracy.

摘要

背景

低度恶性肌纤维母细胞肉瘤(LGMS)是一种罕见的恶性肿瘤。它没有特定的临床表现,常见于头颈部、四肢等身体部位,肝脏不是其易患部位。

病例总结

我们报告了一例 58 岁男性,右上腹痛 11 天。增强计算机断层扫描(CECT)、CE 磁共振成像和 CE 超声(US)均显示右肝有一个囊实性肿块。由于最初的临床诊断是肝囊腺瘤,所以进行了手术切除,术后病理提示肝 LGMS。3 个月的随访显示患者恢复良好。然而,在 7 个月的随访中,二维 US 和 CECT 显示右中腹部疑似转移病灶。

结论

肝 MS 极为罕见,易误诊,更多病例有助于提高认识和诊断准确性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa77/9453762/6e7713779c63/WJG-28-4456-g004.jpg

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