ČESKÁ UROLOGIE / CZECH UROLOGY – 1 / 2020
40 PŘEHLEDOVÝ ČLÁNEK Ces Urol 2020; 24(1): 26–41 30. El‑Hashemite N, Walker V, Zhang H, Kwiatkowski DJ. Loss of Tsc1 or Tsc2 induces vascular endothelial growth factor production through mammalian target of rapamycin. Cancer Res. 2003; 63(17): 5173–5177. 31. Chen YB, Mirsadraei L, Jayakumaran G, et al. Somatic Mutations of TSC2 or MTOR Characterize a Morphologically Distinct Subset of Sporadic Renal Cell Carcinoma With Eosinophilic and Vacuolated Cytoplasm. Am J Surg Pathol. 2019; 43(1): 121–131. 32. Franz DN, Budde K, Kingswood JC, et al. Effect of everolimus on skin lesions in patients treated for subependymal giant cell astrocytoma and renal angiomyolipoma: final 4-year results from the randomized EXIST-1 and EXIST-2 studies. J Eur Acad Dermatol Venereol. 2018; 32(10): 1796–1803. 33. Bissler JJ, Kingswood JC, Radzikowska E, et al. Everolimus long‑term use in patients with tuberous sclerosis complex: Four‑year update of the EXIST-2 study. PLoS One. 2017; 12(8): e0180939. 34. Bissler JJ, Kingswood JC, Radzikowska E, et al. Everolimus for angiomyolipoma associated with tuberous sclerosis complex or sporadic lymphangioleiomyomatosis (EXIST-2): a multicentre, randomised, double‑blind, placebo‑controlled trial. Lancet 2013; 381(9869): 817–824. 35. Staehler M, Sauter M, Helck A, et al. Nephron‑sparing resection of angiomyolipoma after sirolimus pretreatment in patients with tuberous sclerosis. Int Urol Nephrol. 2012; 44(6): 1657–1661. 36. Ürge T, Pitra T, Chudáček Z, et al. Nové trendy v léčbě renalního angiomyolipomu. Ces Urol. 2015; 19(2): 106–117. 37. Moch H, Cubilla AL, Humphrey PA, Reuter VE, Ulbright TM. The 2016 WHO Classification of Tumours of the Urinary System and Male Genital Organs‑Part A: Renal, Penile, and Testicular Tumours. Eur Urol. 2016; 70(1): 93–105. 38. Hora M, Ürge T, Kalusová K, et al. Novelizovaná klasifikace nádorů ledvin 2013 (International Society of Urological Pathology Vancouver Classification of Renal Neoplasia). Ces Urol 2014; 18(1): 9–20. 39. Schmidt LS, Linehan WM. Hereditary leiomyomatosis and renal cell carcinoma. Int J Nephrol Reno‑ vasc, DiS. 2014; 7: 253–260. 40. Trpkov K, Hes O, Agaimy A, et al. Fumarate Hydratase‑deficient Renal Cell Carcinoma Is Strongly Correlated With Fumarate Hydratase Mutation and Hereditary Leiomyomatosis and Renal Cell Carcinoma Syndrome. Am J Surg Pathol. 2016; 40(7): 865–875. 41. Pivovarcikova K, Martinek P, Grossmann P, et al. Fumarate hydratase deficient renal cell carcinoma: Chromosomal numerical aberration analysis of 12 cases. Ann Diagn Pathol. 2019; 39: 63–68. 42. Kuroda N, Ohe C, Kato I, et al. Review of hereditary leiomyomatosis renal cell carcinoma with focus on clinical and pathobiological aspects of renal tumors. Pol J Pathol. 2017; 68(4): 284–290. 43. Plevová P, Hladíková A, Tesařová M. Hereditary leiomyomatosis and renal cell cancer – HLRCC/multiple cutaneous and uterine leimomyomatosis – MCUL. Klin Onkol. 2012; 25 Suppl: S55–58. 44. PrzybycinCG, Magi‑Galluzzi C, McKenney JK. Hereditary syndromeswith associated renal neoplasia: a practi‑ cal guide to histologic recognition in renal tumor resection specimens. Adv Anat Pathol. 2013; 20(4): 245–263. 45. Choyke PL, Walther MM, Glenn GM, et al. Imaging features of hereditary papillary renal cancers. J Comput Assist Tomogr. 1997; 21(5): 737–741. 46. Choueiri TK, Vaishampayan U, Rosenberg JE, et al. Phase II and biomarker study of the dual MET/ VEGFR2 inhibitor foretinib in patients with papillary renal cell carcinoma. J Clin Oncol. 2013; 31(2): 181–186. 47. Schmidt LS, Nickerson ML, Angeloni D, et al. Early onset hereditary papillary renal carcinoma: germ‑ line missense mutations in the tyrosine kinase domain of the met proto‑oncogene. J Urol. 2004; 172(4 Pt 1): 1256–1261. 48. Menko FH, van Steensel MA, Giraud S, et al. Birt‑Hogg‑Dubé syndrome: diagnosis and management. Lancet Oncol. 2009; 10(12): 1199–1206.
Made with FlippingBook
RkJQdWJsaXNoZXIy NDA4Mjc=