手术治疗后经组织病理学诊断为巨大肾脏利肌瘤的罕见病例:病例报告

IF 0.6 Q4 SURGERY
Anak Agung Ngurah Krisnanta Adnyana, Novitasari, I Wayan Suarsana, Ida Bagus Oka Widya Putra
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引用次数: 0

摘要

简介肾细肌瘤是一种罕见的肾肿瘤,起源于平滑肌。在现有的所有肾脏良性肿瘤中,肾细肌瘤是最不常见的肾脏良性肿瘤之一:我们报告了一例 43 岁男性的病例,患者主诉左上腹可触及肿块、腹部不适和血尿。对比增强 CT 扫描显示左肾上有一异质实性肿块,与左腹壁粘连,并将脾脏推向头颅。患者接受了根治性肾切除术,组织病理结果显示为肾癌。术后两周,患者无任何症状:讨论:肾脏利肌瘤的影像学检查可提供线索,一般发现肿瘤边缘清晰,无局部侵犯。在我们的病例中,术前 CT 检查结果显示肾脏肿块与腹壁粘连,因此初步诊断并不明确。只有通过组织病理学检查才能明确诊断:结论:根治性肾切除术仍然是术前诊断不明确时的主要治疗方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
A rare case of large renal leiomyoma diagnosed histopathologically after surgical management: A case report.

Introduction: Renal leiomyoma is a rare renal tumor that originates from smooth muscle. Among all existing benign renal tumors, leiomyoma is one of the least common benign renal tumors.

Case presentation: We report of a case report of a 43-year-old male complaints of palpable mass on the upper left abdomen, abdominal discomfort and hematuria. Contrast-enhanced CT scan revealed a solid heterogenous mass on the left kidney, adherent to the left abdominal wall and pushed the spleen cranially. Patient underwent radical nephrectomy and histopathology results revealed leiomyoma. Two weeks after surgery, the patient was asymptomatic.

Discussion: Imaging of renal leiomyoma may provide a clue with a general finding of a well-defined tumor margin and no local invasion. In our case preoperative CT findings made the initial diagnosis inconclusive since it showed the renal mass was adherent to the abdominal wall. Definitive diagnosis was only possible through histopathologic examination.

Conclusion: Radical nephrectomy remains as the mainstay of treatment in inconclusive preoperative diagnosis.

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CiteScore
1.10
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审稿时长
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