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腹壁低度恶性黏液纤维肉瘤:坦桑尼亚的一例罕见病例报告

Low grade myxofibrosarcoma of the abdominal wall: A rare case report from Tanzania.

作者信息

Nkenguye William, Suleiman Jamil, Jaffer Shaneabbas, Hassan Orujul, Lodhia Jay

机构信息

Department of Epidemiology and Applied Biostatistics, Kilimanjaro Christian Medical University College, P.O. Box 2240, Moshi, Tanzania; Kilimanjaro Clinical Research Institute, Kilimanjaro Christian Medical Centre, P.O. Box 3010, Moshi, Tanzania.

Department of General Medicine, Tiba healthcare Specialized Polyclinic, Upanga, Dar-es-Salaam, Tanzania.

出版信息

Int J Surg Case Rep. 2025 Feb;127:111001. doi: 10.1016/j.ijscr.2025.111001. Epub 2025 Jan 31.

Abstract

INTRODUCTION AND IMPORTANCE

Myxofibrosarcoma (MFS) is a rare malignant soft tissue sarcoma, typically affecting older adults and commonly arising in the extremities. Its occurrence in younger individuals and in atypical locations, such as the abdominal wall, is uncommon.

CASE PRESENTATION

A 27-year-old female presented with a three-year history of a progressively enlarging, painless mass on the left lateral aspect of her abdomen. Initial imaging suggested a benign lesion; however, histopathological examination of the excised mass revealed a spindle cell neoplasm with myxoid changes. Immunohistochemistry confirmed a diagnosis of low-grade MFS. The patient underwent surgical excision with clear margins and remains under regular follow-up with no signs of recurrence to date.

CLINICAL DISCUSSION

This case underscores the diagnostic challenges of MFS, particularly in younger patients and atypical anatomical locations. The nonspecific imaging features highlight the necessity of histopathological examination for accurate diagnosis. Surgical excision with clear margins remains the cornerstone of MFS treatment, and the absence of adverse features in this case negated the need for adjuvant therapy. Regular follow-up is essential due to the high propensity for local recurrence.

CONCLUSION

This case contributes to the limited data on MFS in sub-Saharan Africa, emphasizing the need for increased awareness and reporting to better understand its epidemiology and inform management strategies in this region.

摘要

引言与重要性

黏液纤维肉瘤(MFS)是一种罕见的恶性软组织肉瘤,通常影响老年人,常见于四肢。其在年轻个体以及非典型部位(如腹壁)发生的情况并不常见。

病例介绍

一名27岁女性,左侧腹部外侧有一个逐渐增大的无痛性肿块,病史三年。初始影像学检查提示为良性病变;然而,对切除肿块的组织病理学检查显示为具有黏液样改变的梭形细胞瘤。免疫组织化学确诊为低级别MFS。患者接受了切缘清晰的手术切除,目前仍在定期随访中,至今无复发迹象。

临床讨论

该病例强调了MFS的诊断挑战,尤其是在年轻患者和非典型解剖部位。非特异性的影像学特征凸显了组织病理学检查对于准确诊断的必要性。切缘清晰的手术切除仍然是MFS治疗的基石,该病例中不存在不良特征,因此无需辅助治疗。由于局部复发倾向较高,定期随访至关重要。

结论

该病例为撒哈拉以南非洲地区关于MFS的有限数据做出了贡献,强调需要提高认识并进行报告,以更好地了解其流行病学情况,并为该地区的管理策略提供依据。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/499d/11840528/f5c8d17c6350/gr1.jpg

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