Hereditary Leiomyomatosis and Renal Cell Cancer (HLRCC) Syndrome.

IF 1 4区 医学 Q4 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING Journal of the Belgian Society of Radiology Pub Date : 2024-09-11 eCollection Date: 2024-01-01 DOI:10.5334/jbsr.3687
Karel Mercken, Brecht Van Berkel, Liesbeth De Wever
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Abstract

In hereditary leiomyomatosis and renal cell carcinoma syndrome, fumarate hydratase-deficient renal cell carcinomas typically present as aggressive, unilateral, often cystic masses with heterogeneous enhancement. These tumors can metastasize early, making appropriate imaging and staging critical for diagnosis and management. Teaching point: When a renal lesion suspected of RCC is identified in a patient with cutaneous and uterine leiomyomas, HLRCC should be evaluated, which is important for future genetic counseling.

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遗传性骨髓瘤病和肾细胞癌(HLRCC)综合征。
在遗传性骨髓瘤病和肾细胞癌综合征中,富马酸氢化酶缺陷型肾细胞癌通常表现为侵袭性、单侧、常为囊性肿块并伴有异质强化。这些肿瘤可早期转移,因此适当的成像和分期对诊断和治疗至关重要。教学要点:当在患有皮肤和子宫肌瘤的患者中发现疑似 RCC 的肾脏病变时,应评估 HLRCC,这对未来的遗传咨询非常重要。
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来源期刊
Journal of the Belgian Society of Radiology
Journal of the Belgian Society of Radiology Medicine-Radiology, Nuclear Medicine and Imaging
CiteScore
0.70
自引率
5.00%
发文量
96
期刊介绍: The purpose of the Journal of the Belgian Society of Radiology is the publication of articles dealing with diagnostic and interventional radiology, related imaging techniques, allied sciences, and continuing education.
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