肾细胞癌一例瘤内动脉瘤和肾外同步囊性肿瘤。

Case Reports in Urology Pub Date : 2021-04-06 eCollection Date: 2021-01-01 DOI:10.1155/2021/8878429
Supun De Silva, Lalani De Silva, Susantha De Silva, Priyani Amarathunga
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引用次数: 0

摘要

背景:肾细胞癌是一种起源于肾脏的异质性恶性肿瘤。我们报告一例肾细胞癌合并两个非常罕见的肿瘤,即一个巨大的瘤内动脉瘤和在主要肿瘤外的同步肾外囊性肿瘤。案例演示。31岁女性,表现为无痛性血尿及腰部疼痛,x线检查诊断为肾大肿块,大小为15 × 9 × 8.5 cm,病灶内动脉瘤大小为4.5 × 3.5 cm。在手术中,除了肾肿块外,还在肾前内侧发现了一个单独的囊性肿瘤,尺寸为5 × 4.5 × 4 cm,血管供应明显。主要肿瘤的组织学符合t(6:11)型小眼相关转录因子(MiT)家族易位RCC。动脉瘤在组织学上为静脉源性,影像学上可证实为动静脉瘘。肾外囊肿也表现出与主要肿瘤相似的组织学,没有淋巴结变性的证据。讨论。虽然很少有病例报道与肾肿瘤相关的各种血管异常,但这是第一例发现位于恶性肾肿块内的动静脉瘘伴继发性静脉动脉瘤的病例。同样,没有实性肾细胞癌合并肾外恶性囊性结节的报道。肾外恶性囊肿的预后和肿瘤学意义尚不清楚。这两种不同寻常的特征都没有在术前影像学上得到正确的识别。当有病理报告时,回顾术前影像有助于克服对复杂病例做出最终诊断的困难。结论:rcc可出现动静脉瘘、静脉动脉瘤等血管异常,并可合并肾外恶性囊性结节。
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An Intratumoral Aneurysm and an Extrarenal Synchronous Cystic Tumour in a Case of a Renal Cell Carcinoma.

Background: Renal cell carcinoma is a heterogeneous group of malignant tumors originating from the kidney. We report a case of a renal cell carcinoma with two very rare associates, i.e., a large intratumoral aneurysm and a synchronous extrarenal cystic tumor outside the main tumor. Case Presentation. A 31-year-old woman, who presented with painless hematuria and loin pain, was diagnosed to have a large renal mass measuring 15 × 9 × 8.5 cm with an intralesional arterial aneurysm measuring 4.5 × 3.5 cm on radiological examination. During surgery, a separate cystic tumor measuring 5 × 4.5 × 4 cm with distinct vascular supply was noted anteromedial to the kidney, in addition to the renal mass. The histology of the main tumor was compatible with t(6:11) type microphthalmia-associated transcription factor (MiT) family translocation RCC. The aneurysm was of venous origin histologically, and a radiologically demonstrable arteriovenous fistula was recognized retrospectively. The extrarenal cyst has also showed similar histology to that of main tumor and had no evidence of a degenerated lymph node. Discussion. Although few cases were reported with various vascular anomalies associated with a renal tumor, this is the first ever case to find an arteriovenous fistula with a secondary venous aneurysm located inside a malignant renal mass. Similarly, no solid RCC is reported to present with an extrarenal malignant cystic nodule. The prognostic and oncological significance of the extrarenal malignant cyst is unclear. Both of these extraordinary features of this case were not properly identified on preoperative imaging. Reviewing the preoperative imaging when pathology reports are available helps to overcome difficulties in making the final diagnosis of complex cases.

Conclusion: RCCs can house vascular anomalies like arteriovenous fistula and venous aneurysms and can exist with concomitant extrarenal malignant cystic nodules.

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