Spermatic cord liposarcoma presented as scrotal swelling: a case report

IF 0.5 Q4 UROLOGY & NEPHROLOGY African Journal of Urology Pub Date : 2024-09-06 DOI:10.1186/s12301-024-00446-x
Mohamed Salah Ayyad, Ibrahim Elgaml, Alrawy Ali Mohammad, Amr Mohamed Rizq, Samira Ebrahim
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Abstract

Liposarcoma is considered the most common among spermatic cord sarcomas. It usually presents as a progressively enlarging inguinoscrotal mass. The resemblance between the spermatic cord liposarcoma and the inguinal hernia allows the swelling to be tolerated for a long duration giving time for hematogenous dissemination. In this article, we share the experience of a unique case of metastatic liposarcoma of the spermatic cord that showed a stationary course of the lower abdominal satellite lesions on follow-up following palliative resection. We present a case of a 53-year-old male with progressively enlarging painless scrotal swelling over 1-year duration. A heterogeneous lesion of the right hemiscrotum and spermatic cord with non-specific radiological features was described by imaging. Two lower abdominal skip lesions were also discovered synchronously in addition to the primary one and were designated inoperable as they were adherent to the nearby bowel loops. The patient underwent cytoreductive surgery of the primary tumour which was proven to be an undifferentiated liposarcoma with free safety margins based on histopathology. Finally, the patient was referred for adjuvant chemotherapy and sequential follow-up. Despite being a rare tumour, the radiologist should always consider the liposarcoma of the spermatic cord in the differential diagnosis of inguinoscrotal lesions even in the absence of typical imaging features. The diagnosis and management of spermatic cord liposarcoma remain a challenge with no clear accepted guidelines.
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表现为阴囊肿胀的精索脂肪肉瘤:病例报告
脂肪肉瘤被认为是精索肉瘤中最常见的一种。它通常表现为逐渐增大的腹股沟肿块。精索脂肪肉瘤与腹股沟疝之间的相似性使得肿物可以长期存在,从而为血行播散提供了时间。在本文中,我们分享了一例独特的精索转移性脂肪肉瘤病例的经验,该病例在姑息性切除术后的随访中发现下腹部卫星病灶呈静止状态。我们报告了一例 53 岁男性的病例,他的无痛性阴囊肿物在 1 年内逐渐增大。影像学描述了右侧半阴囊和精索的异质性病变,具有非特异性放射学特征。除原发病灶外,还同步发现了两个下腹部跳部病灶,由于与附近肠襻粘连,无法手术。患者接受了原发肿瘤的细胞减灭术,组织病理学证实这是一种未分化脂肪肉瘤,安全边缘游离。最后,患者被转诊接受辅助化疗和连续随访。尽管精索脂肪肉瘤是一种罕见肿瘤,但放射科医生在鉴别诊断阴囊腹股沟病变时,即使没有典型的影像学特征,也应始终考虑精索脂肪肉瘤。精索脂肪肉瘤的诊断和治疗仍是一项挑战,目前尚无明确的公认指南。
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来源期刊
African Journal of Urology
African Journal of Urology UROLOGY & NEPHROLOGY-
CiteScore
1.00
自引率
0.00%
发文量
58
审稿时长
9 weeks
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