Radiologic and pathologic correlation of a renal venous hemangioma

被引:2
|
作者
Elek, Alperen [1 ]
Kwon, Jung Woo [2 ]
Ertugrul, Sena [3 ]
Oren, Nisa Cem [4 ]
机构
[1] Ege Univ, Fac Med, Erzene Ave, TR-35040 Izmir, Turkiye
[2] Univ Chicago, Fac Med, Dept Pathol, 5801 S Ellis Ave, Chicago, IL 60637 USA
[3] Univ Hlth Sci, Gulhane Fac Med, Emrah Ave, TR-06018 Ankara, Turkiye
[4] Univ Chicago, Fac Med, Dept Radiol, 5801 S Ellis Ave, Chicago, IL 60637 USA
关键词
Renal; Venous; Hemangioma; MRI; CT; Pathology; CELL CARCINOMA; SPONTANEOUS RUPTURE; SIGNAL INTENSITY; FEATURES; KIDNEY; TUMORS; CT;
D O I
10.1007/s13691-023-00626-6
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Renal hemangiomas, including the rare subtype of venous hemangioma, are typically non-cancerous, often asymptomatic, and usually discovered incidentally during imaging studies. Here, we report a unique case of a 59-year-old African-American female with a renal venous hemangioma that initially mimicked papillary-type renal cell carcinoma (RCC-pt) on imaging studies. The patient's presentation included a long history of rectal bleeding and an incidental discovery of a hypoattenuating mass in the left kidney during a contrast-enhanced CT scan. Renal MRI revealed a 3.5 cm left renal lower pole mass, presenting as heterogeneously hyperintense on T1-weighted images and hypointense on T2-weighted images, with gradual mild enhancement post-contrast. Subsequent total nephrectomy confirmed the histopathological diagnosis of a venous hemangioma. This case underlines the need for recognizing unique imaging features of renal venous hemangiomas, contributing to the differential diagnosis of T2 dark hypoenhancing renal masses. Correct interpretation may prevent unnecessary invasive procedures and operations, thereby improving patient management and outcomes.
引用
收藏
页码:227 / 232
页数:6
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