Çocukluk Yaş Grubunda Benign Renal Kitlesel Lezyonlar

Authors

Deniz Kızmazoğlu
Demet Alaygut

Synopsis

In childhood, renal masses are mostly detected incidentally during routine examinations or evaluations for other conditions. Since malignant renal masses are rare, accounting for only 7% of all pediatric cancers, accurately differentiating benign from malignant lesions is of paramount importance. This differentiation requires a multidisciplinary approach involving pediatric nephrology, pediatric oncology, radiology, surgery, and pathology. During the diagnostic process, cross-sectional imaging modalities such as ultrasonography (US), computed tomography (CT), and magnetic resonance imaging (MRI) are utilized alongside clinical history, physical examination, and laboratory findings. While US enables the differentiation between cystic and solid structures, MRI stands out due to its high soft-tissue contrast and lack of radiation exposure. Benign renal lesions identified in children include simple cysts, which are the most common and classified under Bosniak Categories 1 and 2; angiomyolipomas, which are associated with tuberous sclerosis in 80% of cases and can be treated with mTOR inhibitors; metanephric adenoma, a rare epithelial/stromal tumor; oncocytoma, which contains a central scar; reninoma, characterized by hypertension, hypokalemia, and high renin activity; ossifying renal tumor of infancy, causing painless gross hematuria; multicystic cystic nephroma, which may require surgical resection; and renal pseudotumors secondary to focal pyelonephritis or congenital anomalies.

References

Fernandez CV, Geller JJ, Ehrlich PF et al. Renal Tumors, In: Pizzo PA, Poplack DG. Principles and Practice of Pediatric Oncology. 7 th ed. Philadelphia, Wolters Kluwer. 2021. Chapter 24, p.637-92.

O'Connor SD, Pickhardt PJ, Kim DH, et al. Incidental finding of renal masses at unenhanced CT: prevalence and analysis of features for guiding management. AJR Am J Roentgenol 2011; 197:139.

Carrim ZI, Murchison JT. The prevalence of simple renal and hepatic cysts detected by spiral computed tomography. Clin Radiol 2003; 58:626.

Herts BR, Silverman SG, Hindman NM, et al. Management of the Incidental Renal Mass on CT: A White Paper of the ACR Incidental Findings Committee. J Am Coll Radiol 2018; 15:264.

Tada S, Yamagishi J, Kobayashi H, et al. The incidence of simple renal cyst by computed tomography. Clin Radiol 1983; 34:437.

Bosniak MA. The current radiological approach to renal cysts. Radiology 1986; 158:1.

Thompson RH, Kurta JM, Kaag M, et al. Tumor size is associated with malignant potential in renal cell carcinoma cases. J Urol 2009; 181:2033.

Rendon RA, Stanietzky N, Panzarella T, et al. The natural history of small renal masses. J Urol 2000; 164:1143.

Suzuki R, Gondo A, Jimi K, et al. [Two cases of incidentally detected renal arteriovenous fistula over ten years after renal biopsy]. Nihon Jinzo Gakkai Shi 2016; 58:33.

Kwon T, Jeong IG, Yoo S, et al. Role of MRI in indeterminate renal mass: diagnostic accuracy and impact on clinical decision making. Int Urol Nephrol 2015; 47:585.

Atri M, Tabatabaeifar L, Jang HJ, et al. Accuracy of Contrast-enhanced US for Differentiating Benign from Malignant Solid Small Renal Masses. Radiology 2015; 276:900.

Graversen JA, Mues AC, Pérez-Lanzac de Lorca A, Landman J. Active surveillance of renal cortical neoplasms: a contemporary review. Postgrad Med 2011; 123:105.

Kang SK, Zhang A, Pandharipande PV, et al. DWI for Renal Mass Characterization: Systematic Review and Meta-Analysis of Diagnostic Test Performance. AJR Am J Roentgenol 2015; 205:317.

Mytsyk Y, Dutka I, Yuriy B, et al. Differential diagnosis of the small renal masses: role of the apparent diffusion coefficient of the diffusion-weighted MRI. Int Urol Nephrol 2018; 50:197.

Newatia A, Khatri G, Friedman B, Hines J. Subtraction imaging: applications for nonvascular abdominal MRI. AJR Am J Roentgenol 2007; 188:1018.

Tsili AC, Argyropoulou MI, Gousia A, et al. Renal cell carcinoma: value of multiphase MDCT with multiplanar reformations in the detection of pseudocapsule. AJR Am J Roentgenol 2012; 199:379.

Zhang J, Pedrosa I, Rofsky NM. MR techniques for renal imaging. Radiol Clin North Am 2003; 41:877.

Kohashi K, Oda Y, Nakamori M, et al. Multifocal metanephric adenoma in childhood. Pathol Int. 2009;59(1):49–52

Mei H, Zheng L, Zhou C, Tong Q. Metanephric adenoma in a 2-year-old child: case report and immunohistochemical observations. J Pediatr Hematol Oncol. 2010;32(6):489–493

Küpeli S, Baydar DE, Canakl F, et al. Metanephric adenoma in a 6-year-old child with hemihypertrophy. J Pediatr Hematol Oncol. 2009;31(6):453–455

Hartman DJ, Maclennan GT. Renal metanephric adenoma J Urol. 2007;178(3 Pt 1):1058

Xi S, Chen H, Wu X, et al. Malignant renal angiomyolipoma with metastases in a child. Int J Surg Pathol. 2014;22(2): 160–166.

Astigueta JC, Abad MA, Pow-Sang MR, et al. Epithelioid angiomyolipoma: a rare variant of renal angiomyolipoma. Arch Esp Urol. 2009;62(6):493–497.

Siegel MJ, Chung EM. Wilms’ Tumor and Other Pediatric Renal Masses. Magn Reson Imaging Clin N Am 2008; 16: 479-97.

Choh NA, Choh SA, Yousuf R, Jehangir M. A giant aneurysm arising from renal angiomyolipoma in tuberous sclerosis. Arch Dis Child. 2009;94(1):47–48).

Alpin D Malkan, Amos Loh, Armita Bahrami, Fariba Navid, Jamie Coleman, Daniel M Green, Andrew M Davidoff, John A Sandoval. An approach to renal masses in pediatrics Pediatrics 2015 Jan;135(1):142-58. doi: 10.1542/peds.2014-1011.

Ito M, Sugamura Y, Ikari H, Sekine I. Angiomyolipoma of the lung. Arch Pathol Lab Med. 1998;122(11): 1023–1025.

Umeoka S, Koyama T, Miki Y, Akai M, Tsutsui K, Togashi K. Pictorial review of tuberous sclerosis in various organs. Radiographics. 2008;28(7):e32.

Schieda N, Kielar AZ, Al Dandan O, McInnes MD, Flood TA. Ten uncommon and unusual variants of renal angiomyolipoma (AML): radiologic-pathologic correlation. Clin Radiol. 2015 Feb;70(2):206-20.

Silverman SG, Gan YU, Mortele KJ, Tuncali K, Cibas ES. Renal masses in the adult patient: the role of percutaneous biopsy Radiology. 2006;240(1):6.

Sooriakumaran P, Gibbs P, Coughlin G, Attard V, Elmslie F, Kingswood C, Taylor J, Corbishley C, Patel U, Anderson C. Angiomyolipomata: challenges, solutions, and future prospects based on over 100 cases treated. BJU Int. 2010 Jan;105(1):101-6.

Samuels JA. Treatment of Renal Angiomyolipoma and Other Hamartomas in Patients with Tuberous Sclerosis Complex. Clin J Am Soc Nephrol 2017;12:1196-1202.

Bissler JJ, Franz DN, Frost MD et al. The effect of everolimus on renal angiomyolipoma in pediatric patients vith tuberous sclerosis being treated for subependymal giant cell astrocytoma. Pediatr Nephrol 2018;33(1):101-109.

Versteege I, Sévenet N, Lange J, et al. Truncating mutations of hSNF5/INI1 in aggressive paediatric cancer. Nature. 1998;394(6689):203–206.

Lee EY. CT imaging of mass-like renal lesions in children. Pediatr Radiol. 2007; 37(9):896–907

Israel GM, Silverman SG. The incidental renal mass. Radiol Clin North Am. 2011; 49(2):369–383.

Ciftci AO, Talim B, Senocak ME et al. Renal Oncocytoma: diagnostic and therapeutic aspects. J Pediatr Surg 2000;35(9):1396-8.

Perez-Ordonez B, Hamed G, Campbell S, Erlandson RA, Russo P, Gaudin PB, Reuter VE Renal oncocytoma: a clinicopathologic study of 70 cases Am J Surg Pathol. 1997;21(8):871

Yusenko MV. Molecular Pathology of renal oncocytoma: a review. Int J Urol 2010;17(7):602-12.

Bhatt S, MacLennan G, Dogra V Renal pseudotumors. AJR Am J Roentgenol. 2007;188(5):1380.

Craig WD, Wagner BJ, Travis MD Pyelonephritis: radiologic-pathologic review. Radiographics. 2008;28(1):255.

Mehra BR, Thawait AP, Akther MJ, Narang RR. Multicystic nephroma masquerading as Wilms’ tumor: a clinical diagnostic challenge. Saudi J Kidney Dis Transpl. 2011;22(4):774–778

Babu S, Agarwal R, Narayansamy K, Rajendranath R, Balasubramanian S. Cystic renal neoplasm causing hypertension in a 2-year-old child. Saudi J Kidney Dis Transpl. 2011;22(4):779–781.

Bhardwaj AK, Sharma PD, Mittal A, Sharma A. Bilateral cystic nephroma with pleuropulmonary blastoma. BMJ Case Rep. 2011

Kacar A, Azili MN, Cihan BS, Demir HA, Tiryaki HT, Argani P. Metanephric stromal tumor: a challengingdiagnostic entity in children. J Pediatr Surg. 2011;46(12):e7–e10

Argani P, Beckwith JB. Metanephric stromal tumor: report of 31 cases of a distinctive pediatric renal neoplasm. Am J Surg Pathol. 2000; 24(7):917–926.

Xu B, Zhang Q, Jin J. Hypertension secondary to reninoma treated with laparoscopic nephron-sparing surgery in a child. Urology. 2012;80(1):210–213

Gottardo F, Cesari M, Morra A, Gardiman M, Fassina A, Dal Bianco M. A kidney tumor in an adolescent with severe hypertension and hypokalemia: an uncommon case—case report and review of the literature on reninoma. Urol Int. 2010;85(1):121–124.

Markey RB, MacLennan GT. Juxtaglomerular cell tumor of the kidney. J Urol. 2006;175(2):730.

Wenbin Guan, Yu Yan , Wenguang He , Meng Qiao , Yi Liu , Yanhua Wang , Bo Jiang , Wenwei Yu , Ruifen Wang , Lifeng Wang Ossifying renal tumor of infancy (ORIT): The clinicopathological and cytogenetic feature of two cases and literature review Pathol Res Pract 2016 Nov;212(11):1004-1009. doi: 10.1016/j.prp.2016.08.008. Epub 2016 Sep 2

S.H. Lee, Y.H. Choi, W.S. Kim, et al., Ossifying renal tumor of infancy: findingsat ultrasound, CT and MRI, Pediatr. Radiol. 44 (2014) 625–628.

L.H. Lowe, B.H. Isuani, R.M. Heller, et al., Pediatric renal masses: wilms tumorand beyond, Radiographics 20 (2000) 1585–1603.

Merchant SA, Badhe PB. Nephroblastomatosis- pathologic and imaging characteristics. J Postgrad med. 1995;41: 72-80.

Published

October 2, 2021

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