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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="other" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Cancer Urology</journal-id><journal-title-group><journal-title xml:lang="en">Cancer Urology</journal-title><trans-title-group xml:lang="ru"><trans-title>Онкоурология</trans-title></trans-title-group></journal-title-group><issn publication-format="print">1726-9776</issn><issn publication-format="electronic">1996-1812</issn><publisher><publisher-name xml:lang="en">Publishing House ABV Press</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">1178</article-id><article-id pub-id-type="doi">10.17650/1726-9776-2006-2-2-14-21</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>DIAGNOSIS AND TREATMENT OF URINARY SYSTEM TUMORS. RENAL CANCER</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>ДИАГНОСТИКА И ЛЕЧЕНИЕ ОПУХОЛЕЙ МОЧЕПОЛОВОЙ СИСТЕМЫ. Рак почки</subject></subj-group><subj-group subj-group-type="article-type"><subject></subject></subj-group></article-categories><title-group><article-title xml:lang="en">Renal angiomyolipoma: diagnosis and treatment</article-title><trans-title-group xml:lang="ru"><trans-title>Ангиомиолипома почки: диагностика и лечение</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Matveyev</surname><given-names>V. B.</given-names></name><name xml:lang="ru"><surname>Матвеев</surname><given-names>В. Б.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Sorokin</surname><given-names>K. V.</given-names></name><name xml:lang="ru"><surname>Сорокин</surname><given-names>К. В.</given-names></name></name-alternatives><address><country country="RU">Russian Federation</country></address><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">N.N. Blokhin Russian Cancer Research Center, Russian Academy of Medical Sciences</institution></aff><aff><institution xml:lang="ru">ГУ РОНЦ им. Н.Н. Блохина РАМН</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2006-06-30" publication-format="electronic"><day>30</day><month>06</month><year>2006</year></pub-date><volume>2</volume><issue>2</issue><issue-title xml:lang="en"/><issue-title xml:lang="ru"/><fpage>14</fpage><lpage>21</lpage><history><date date-type="received" iso-8601-date="2020-02-18"><day>18</day><month>02</month><year>2020</year></date><date date-type="accepted" iso-8601-date="2020-02-18"><day>18</day><month>02</month><year>2020</year></date></history><permissions><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://oncourology.abvpress.ru/oncur/article/view/1178">https://oncourology.abvpress.ru/oncur/article/view/1178</self-uri><abstract xml:lang="en"><p>Renal angiomyolipoma (RAML) is a most common benign tumor. It consists of fat, vascular, epithelioid cells, and smooth-muscle elements. Two types are described: isolated RAML and RAML associated with tuberous sclerosis. Tuberous sclerosis-associated RAML accounts for 20% of the tumors; these lesions are typically larger than RAMLs; they are often bilateral and multiple and tend to grow. The adequate diagnostic tools for RAML include ultrasonography and computed tomography. Fine-needle biopsy can elucidate the diagnosis of RAML in difficult cases. Most minor lesions are asymptomatic and those smaller than 5 cm need only a regular follow-up without intervention. Nephronsparing surgery is recommended if large RAMLs or symptomatic lesions are present. In these cases, the optimum treatment is partial nephrectomy or selective renal embolization. Angioembolization of RAML is a new technique which obviates surgical disadvantages. Positive immunoreactivity to HMB-45 and α-smooth muscle actin is diagnostic for RAML and distinguishes it from renal cell carcinoma.</p></abstract><trans-abstract xml:lang="ru"><p>.</p></trans-abstract><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">1. Stone C.H., Lee M.W., Amin M.B. et al. Renal Angiomyolipoma. Further Immunophenotypic Characterization of an Expanding Morphologic Spectrum. Arch Pathol Lab Med 2001; 125: 751–8.</mixed-citation><mixed-citation xml:lang="ru">Stone C.H., Lee M.W., Amin M.B. et al. Renal Angiomyolipoma. Further Immunophenotypic Characterization of an Expanding Morphologic Spectrum. Arch Pathol Lab Med 2001; 125: 751–8.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">2. Nelson C.P., Sanda M.G. Contemporary diagnosis and management of renal angiomyolipoma. 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