Çocukluk Yaş Grubunda Benign Renal Kitlesel Lezyonlar
Özet
Çocukluk çağında renal kitleler çoğunlukla rutin incelemeler veya diğer hastalıkların değerlendirilmesi sırasında insidental olarak tespit edilir. Renal malign kitleler tüm çocukluk çağı kanserlerinin %7'sini oluşturacak kadar nadir olduğundan, tespit edilen kitlesel lezyonların benign ve malign ayrımının doğru şekilde yapılması büyük önem taşır. Bu ayrımda pediatrik nefroloji, pediatrik onkoloji, radyoloji, cerrahi ve patoloji uzmanlarını kapsayan multidisipliner bir yaklaşım benimsenmelidir. Tanı aşamasında klinik öykü, fizik muayene ve laboratuvar bulgularının yanı sıra ultrasonografi (US), bilgisayarlı tomografi (BT) ve manyetik rezonans görüntüleme (MRG) gibi kesitsel görüntüleme yöntemlerinden yararlanılır. US kistik ve solid yapıların ayırt edilmesini sağlarken; yüksek doku kontrastına sahip MRG, radyasyon riski içermemesi nedeniyle ön plana çıkar. Çocuklarda saptanan benign renal lezyonlar arasında en sık rastlanan ve Bosniak Kategori 1 ile 2 altında değerlendirilen basit kistler; %80 olguda tuberoskleroza eşlik eden ve mTOR inhibitörleri ile tedavi edilebilen anjiyomiyolipomlar; nadir epitelyal/stromal tümörlerden olan metanefrik adenom; merkezinde skar dokusu barındıran onkositom; hipertansiyon, hipokalemi ve yüksek renin aktivitesiyle karakterize reninoma; ağrısız makroskopik hematüriye yol açan infantın ossifiye renal tümörü; cerrahi rezeksiyon gerektirebilen multikistik kistik nefroma ve fokal piyelonefrit veya konjenital anomalilere sekonder gelişen renal psödotümörler bulunmaktadır.
Referanslar
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.