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

被引:0
作者
Nkenguye, William [1 ,2 ]
Suleiman, Jamil [3 ]
Jaffer, Shaneabbas [3 ]
Hassan, Orujul [4 ]
Lodhia, Jay [5 ,6 ,7 ]
机构
[1] Kilimanjaro Christian Med Univ Coll, Dept Epidemiol & Appl Biostat, POB 2240, Moshi, Tanzania
[2] Kilimanjaro Clin Res Inst, Kilimanjaro Christian Med Ctr, POB 3010, Moshi, Tanzania
[3] Tiba Healthcare Specialized Polyclin, Dept Gen Med, Dar Es Salaam, Tanzania
[4] Aga Khan Univ, Dept Family Med, Dar Es Salaam 2289, Tanzania
[5] Kilimanjaro Christian Med Ctr, Dept Gen Surg, POB 3010, Moshi, Tanzania
[6] Kilimanjaro Christian Med Univ Coll, Fac Med, POB 2240, Moshi, Tanzania
[7] Manchester Univ NHS Fdn Trust, Dept Renal & Pancreat Transplantat, Manchester, England
关键词
Myxofibrosarcoma; Abdomen; Soft tissue sarcoma; Immunohistochemistry; Tanzania;
D O I
10.1016/j.ijscr.2025.111001
中图分类号
R61 [外科手术学];
学科分类号
摘要
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 followup 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.
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