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<article article-type="research-article" dtd-version="1.3" 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" xml:lang="ru"><front><journal-meta><journal-id journal-id-type="publisher-id">nodgo</journal-id><journal-title-group><journal-title xml:lang="ru">Российский журнал детской гематологии и онкологии (РЖДГиО)</journal-title><trans-title-group xml:lang="en"><trans-title>Russian Journal of Pediatric Hematology and Oncology</trans-title></trans-title-group></journal-title-group><issn pub-type="ppub">2311-1267</issn><issn pub-type="epub">2413-5496</issn><publisher><publisher-name>LTD “Graphica”</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="doi">10.21682/2311-1267-2019-6-4-93-96</article-id><article-id custom-type="elpub" pub-id-type="custom">nodgo-559</article-id><article-categories><subj-group subj-group-type="heading"><subject>Research Article</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="ru"><subject>КЛИНИЧЕСКИЕ НАБЛЮДЕНИЯ</subject></subj-group><subj-group subj-group-type="section-heading" xml:lang="en"><subject>CLINICAL CASES</subject></subj-group></article-categories><title-group><article-title>Билатеральная лейомиома надпочечников: редкий случай и дифференциальная диагностика с точки зрения рентгенолога</article-title><trans-title-group xml:lang="en"><trans-title>Bilateral adrenal leiomyoma: a rare case and differential diagnosis from the point of view of the radiologist</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-4164-004X</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Струмила</surname><given-names>Н. А.</given-names></name><name name-style="western" xml:lang="en"><surname>Strumila</surname><given-names>N. A.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Наталия Алексеевна Струмила - врач-рентгенолог, лаборант-исследователь отдела лучевой диагностики НМИЦ ДГОИ им. Дмитрия Рогачева.</p><p>117997, Москва, ул. Саморы Машела, 1</p></bio><bio xml:lang="en"><p>Research Assistant of Department Radiation Diagnosis.</p><p>1 Samory Mashela St., Moscow, 117997</p></bio><email xlink:type="simple">natalya.strumila@fccho-moscow.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0003-1099-9332</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Краснов</surname><given-names>А. С.</given-names></name><name name-style="western" xml:lang="en"><surname>Krasnov</surname><given-names>A. S.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Врач-рентгенолог, научный сотрудник отдела лучевой диагностики НМИЦ ДГОИ им. Дмитрия Рогачева.</p><p>117997, Москва, ул. Саморы Машела, 1</p></bio><bio xml:lang="en"><p>Researcher of Department Radiation Diagnosis.</p></bio><email xlink:type="simple">alexey.krasnov@fccho-moscow.ru</email><xref ref-type="aff" rid="aff-1"/></contrib><contrib contrib-type="author" corresp="yes"><contrib-id contrib-id-type="orcid">https://orcid.org/0000-0001-7317-7104</contrib-id><name-alternatives><name name-style="eastern" xml:lang="ru"><surname>Терещенко</surname><given-names>Г. В.</given-names></name><name name-style="western" xml:lang="en"><surname>Tereshchenko</surname><given-names>G. V.</given-names></name></name-alternatives><bio xml:lang="ru"><p>Кандидат медицинских наук, заведующая рентгенологическим отделением НМИЦ ДГОИ им. Дмитрия Рогачева.</p><p>117997, Москва, ул. Саморы Машела, 1</p></bio><bio xml:lang="en"><p>Cand. of Sci. (Med.), Head of Radiology Department.</p><p>1 Samory Mashela St., Moscow, 117997</p></bio><email xlink:type="simple">Galina.Tereshenko@fccho-moscow.iu</email><xref ref-type="aff" rid="aff-1"/></contrib></contrib-group><aff-alternatives id="aff-1"><aff xml:lang="ru"><institution>ФГБУ «НМИЦДГОИ им. Дмитрия Рогачева» Минздрава России</institution><country>Россия</country></aff><aff xml:lang="en"><institution>Dmitry Rogachev National Medical Research Center of Pediatric Hematology, Oncology and Immunology, Ministry of Health of Russia</institution><country>Russian Federation</country></aff></aff-alternatives><pub-date pub-type="collection"><year>2019</year></pub-date><pub-date pub-type="epub"><day>22</day><month>01</month><year>2020</year></pub-date><volume>6</volume><issue>4</issue><fpage>93</fpage><lpage>96</lpage><permissions><copyright-statement>Copyright &amp;#x00A9; Струмила Н.А., Краснов А.С., Терещенко Г.В., 2020</copyright-statement><copyright-year>2020</copyright-year><copyright-holder xml:lang="ru">Струмила Н.А., Краснов А.С., Терещенко Г.В.</copyright-holder><copyright-holder xml:lang="en">Strumila N.A., Krasnov A.S., Tereshchenko G.V.</copyright-holder><license xml:lang="ru" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>Данная работа распространяется под лицензией Creative Commons Attribution 4.0.</license-p></license><license xml:lang="en" license-type="creative-commons-attribution" xlink:href="https://creativecommons.org/licenses/by/4.0/" xlink:type="simple"><license-p>This work is licensed under a Creative Commons Attribution 4.0 License.</license-p></license></permissions><self-uri xlink:href="https://journal.nodgo.org/jour/article/view/559">https://journal.nodgo.org/jour/article/view/559</self-uri><abstract><p>Лейомиома — доброкачественная опухоль гладкомышечных клеток. Локализация данного образования в надпочечниках является крайне редкой, еще реже встречается поражение обоих надпочечников. В литературе нами было найдено менее 10 описанных случаев возникновения подобной патологии у детей. В статье представлен случай 17-летней девушки с жалобами на тахикардию и повышение давления, у которой впоследствии были выявлены билатеральные образования надпочечников. При гистологической верификации был установлен диагноз лейомиомы.</p></abstract><trans-abstract xml:lang="en"><p>Leiomyoma is a benign tumor of smooth muscle cells. Localization of this formation in the adrenal glands is extremely rare, even less common is the defeat of both adrenal glands. In the literature, we found less than 10 described cases of the occurrence of a similar pathology in children. The article presents a case of a 17-year-old girl with complaints of tachycardia and an increase in pressure, which subsequently revealed bilateral adrenal masses. Histological verification diagnosed leiomyoma.</p></trans-abstract><kwd-group xml:lang="ru"><kwd>образование надпочечника</kwd><kwd>компьютерная томография</kwd><kwd>магнитно-резонансная томография</kwd><kwd>детская онкология</kwd><kwd>доброкачественная опухоль</kwd></kwd-group><kwd-group xml:lang="en"><kwd>adrenal gland mass</kwd><kwd>computed tomography</kwd><kwd>magnetic resonance imaging</kwd><kwd>pediatric oncology</kwd><kwd>benign tumor</kwd></kwd-group></article-meta></front><back><ref-list><title>References</title><ref id="cit1"><label>1</label><citation-alternatives><mixed-citation xml:lang="ru">Ho Y.H., Yap W.M., Chuah K.L. Solitary fibrous tumor of the adrenal gland with unusual immunophenotype: a potential diagnostic problem and a brief review of endocrine organ solitary fibrous tumor. Endocr Pathol 2010;21(2):125-9. doi: m.m07/s12022-010-9113-z.</mixed-citation><mixed-citation xml:lang="en">Ho Y.H., Yap W.M., Chuah K.L. Solitary fibrous tumor of the adrenal gland with unusual immunophenotype: a potential diagnostic problem and a brief review of endocrine organ solitary fibrous tumor. Endocr Pathol 2010;21(2):125-9. doi: m.m07/s12022-010-9113-z.</mixed-citation></citation-alternatives></ref><ref id="cit2"><label>2</label><citation-alternatives><mixed-citation xml:lang="ru">Corti M., Carolis L.D., Veliz L., Campitelli A., Haab G.A. Adrenal Leiomyoma: A Rare Tumor Presented as an Incidentaloma in a Patient with AIDS. Mathews J HIV AIDS 2016;1(1):006.</mixed-citation><mixed-citation xml:lang="en">Corti M., Carolis L.D., Veliz L., Campitelli A., Haab G.A. Adrenal Leiomyoma: A Rare Tumor Presented as an Incidentaloma in a Patient with AIDS. Mathews J HIV AIDS 2016;1(1):006.</mixed-citation></citation-alternatives></ref><ref id="cit3"><label>3</label><citation-alternatives><mixed-citation xml:lang="ru">Lin J., Wasco M.J., Korobkin M., Doherty G., Giordano T.J. Leiomyoma of the adrenal gland presenting as a non-functioning adrenal incidentaloma: case report and review of the literature. Endocr Pathol 2007;18(4):239-43. doi: 10.1007/s12022-008-9013-7.</mixed-citation><mixed-citation xml:lang="en">Lin J., Wasco M.J., Korobkin M., Doherty G., Giordano T.J. Leiomyoma of the adrenal gland presenting as a non-functioning adrenal incidentaloma: case report and review of the literature. Endocr Pathol 2007;18(4):239-43. doi: 10.1007/s12022-008-9013-7.</mixed-citation></citation-alternatives></ref><ref id="cit4"><label>4</label><citation-alternatives><mixed-citation xml:lang="ru">Lack E. Smooth muscle neoplasms. AFIP Atlas of Tumor Pathology, Tumors of the Adrenal Glands and Extraadrenal Paraganglia. Fourth Series. Fascicle, 2007.</mixed-citation><mixed-citation xml:lang="en">Lack E. Smooth muscle neoplasms. AFIP Atlas of Tumor Pathology, Tumors of the Adrenal Glands and Extraadrenal Paraganglia. Fourth Series. Fascicle, 2007.</mixed-citation></citation-alternatives></ref><ref id="cit5"><label>5</label><citation-alternatives><mixed-citation xml:lang="ru">Huei T.J., Lip H.T.C., Rahman M., Arulanantham S. Large adrenal leiomyoma presented as adrenal incidentaloma in an AIDS patient: a rare entity. Med J Malaysia 2017;72(1):65-7. PMID: 28255146.</mixed-citation><mixed-citation xml:lang="en">Huei T.J., Lip H.T.C., Rahman M., Arulanantham S. Large adrenal leiomyoma presented as adrenal incidentaloma in an AIDS patient: a rare entity. Med J Malaysia 2017;72(1):65-7. PMID: 28255146.</mixed-citation></citation-alternatives></ref><ref id="cit6"><label>6</label><citation-alternatives><mixed-citation xml:lang="ru">Rha S.E., Byun J.Y., Jung S.E., Chun H.J., Lee H.G., Lee J.M. Neurogenic tumors in the abdomen: tumor types and imaging characteristics. Radiographics 2003;23(1):29-43. doi: 10.1148/rg.231025050.</mixed-citation><mixed-citation xml:lang="en">Rha S.E., Byun J.Y., Jung S.E., Chun H.J., Lee H.G., Lee J.M. Neurogenic tumors in the abdomen: tumor types and imaging characteristics. Radiographics 2003;23(1):29-43. doi: 10.1148/rg.231025050.</mixed-citation></citation-alternatives></ref><ref id="cit7"><label>7</label><citation-alternatives><mixed-citation xml:lang="ru">Lonergan G.J., Schwab C.M., Suarez E.S., Carlson C.L. From the archives of the AFIP: neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: radiologic-pathologic correlation. Radiographics 2002;22(4):911-34. doi: 10.1148/radiographics.22.4.g02jl15911.</mixed-citation><mixed-citation xml:lang="en">Lonergan G.J., Schwab C.M., Suarez E.S., Carlson C.L. From the archives of the AFIP: neuroblastoma, ganglioneuroblastoma, and ganglioneuroma: radiologic-pathologic correlation. Radiographics 2002;22(4):911-34. doi: 10.1148/radiographics.22.4.g02jl15911.</mixed-citation></citation-alternatives></ref><ref id="cit8"><label>8</label><citation-alternatives><mixed-citation xml:lang="ru">Pages P.M., Dufour C., Fasola S., Michon J., Boutard P., Gentet J.C., Hartmann O. Bilateral adrenal neuroblastoma. Pediatr Blood Cancer 2009;52(2):196-202. doi: 10.1002/pbc.21765.</mixed-citation><mixed-citation xml:lang="en">Pages P.M., Dufour C., Fasola S., Michon J., Boutard P., Gentet J.C., Hartmann O. Bilateral adrenal neuroblastoma. Pediatr Blood Cancer 2009;52(2):196-202. doi: 10.1002/pbc.21765.</mixed-citation></citation-alternatives></ref><ref id="cit9"><label>9</label><citation-alternatives><mixed-citation xml:lang="ru">Papaioannou G., McHugh K. Neuroblastoma in childhood: review and radiological findings. Cancer Imaging 2005;5(1):116-27. doi: 10.1102/1470-7330.2005.0104.</mixed-citation><mixed-citation xml:lang="en">Papaioannou G., McHugh K. Neuroblastoma in childhood: review and radiological findings. Cancer Imaging 2005;5(1):116-27. doi: 10.1102/1470-7330.2005.0104.</mixed-citation></citation-alternatives></ref><ref id="cit10"><label>10</label><citation-alternatives><mixed-citation xml:lang="ru">Blake M.A., Kalra M.K., Maher M.M., Sahani D.V., Sweeney A.T., Mueller P.R., Boland G.W. Pheochromocytoma: an imaging chameleon. Radiographics 2004;Suppl 1:S87-99. doi: 10.1148/rg.24si045506.</mixed-citation><mixed-citation xml:lang="en">Blake M.A., Kalra M.K., Maher M.M., Sahani D.V., Sweeney A.T., Mueller P.R., Boland G.W. Pheochromocytoma: an imaging chameleon. Radiographics 2004;Suppl 1:S87-99. doi: 10.1148/rg.24si045506.</mixed-citation></citation-alternatives></ref><ref id="cit11"><label>11</label><citation-alternatives><mixed-citation xml:lang="ru">Sarathi V. Characteristics of Pediatric Pheochromocytoma/ paraganglioma. Indian J Endocrinol Metab 2017;21(3):470-4. doi: 10.4103/ijem.IJEM_558_16.</mixed-citation><mixed-citation xml:lang="en">Sarathi V. Characteristics of Pediatric Pheochromocytoma/ paraganglioma. Indian J Endocrinol Metab 2017;21(3):470-4. doi: 10.4103/ijem.IJEM_558_16.</mixed-citation></citation-alternatives></ref><ref id="cit12"><label>12</label><citation-alternatives><mixed-citation xml:lang="ru">Prabhu M., Joseph T.T., Shetty N., Chaudhuri S. Saudi J Anaesth 2013;7(2):197-9. doi: 10.4103/1658-354X.114051.</mixed-citation><mixed-citation xml:lang="en">Prabhu M., Joseph T.T., Shetty N., Chaudhuri S. Saudi J Anaesth 2013;7(2):197-9. doi: 10.4103/1658-354X.114051.</mixed-citation></citation-alternatives></ref><ref id="cit13"><label>13</label><citation-alternatives><mixed-citation xml:lang="ru">Johnson P.T., Horton K.M., Fishman E.K. Adrenal mass imaging with multidetector CT: pathologic conditions, pearls, and pitfalls. Radiographics 2009;29(5):1333-51. doi: 10.1148/rg.295095027.</mixed-citation><mixed-citation xml:lang="en">Johnson P.T., Horton K.M., Fishman E.K. Adrenal mass imaging with multidetector CT: pathologic conditions, pearls, and pitfalls. Radiographics 2009;29(5):1333-51. doi: 10.1148/rg.295095027.</mixed-citation></citation-alternatives></ref><ref id="cit14"><label>14</label><citation-alternatives><mixed-citation xml:lang="ru">Mouchet F., Ninane J., Gosseye S., Verellen C., Bonnier C., Evrard P., Cornu G. Leiomyoma of the suprarenal gland in a child with ataxiatelangiectasia. Pediatr Hematol Oncol 1991;8(3):235-41. doi: 10.3109/08880019109033457.</mixed-citation><mixed-citation xml:lang="en">Mouchet F., Ninane J., Gosseye S., Verellen C., Bonnier C., Evrard P., Cornu G. Leiomyoma of the suprarenal gland in a child with ataxiatelangiectasia. Pediatr Hematol Oncol 1991;8(3):235-41. doi: 10.3109/08880019109033457.</mixed-citation></citation-alternatives></ref><ref id="cit15"><label>15</label><citation-alternatives><mixed-citation xml:lang="ru">Jimenez-Heffernan J.A., Hardisson D., Palacios J., Garcia-Viera M., Gamallo C., Nistal M. Adrenal gland leiomyoma in a child with acquired immunodeficiency syndrome. Pediatr Pathol Lab Med 1995;15(6):923-9. doi: 10.3109/15513819509027028.</mixed-citation><mixed-citation xml:lang="en">Jimenez-Heffernan J.A., Hardisson D., Palacios J., Garcia-Viera M., Gamallo C., Nistal M. Adrenal gland leiomyoma in a child with acquired immunodeficiency syndrome. Pediatr Pathol Lab Med 1995;15(6):923-9. doi: 10.3109/15513819509027028.</mixed-citation></citation-alternatives></ref><ref id="cit16"><label>16</label><citation-alternatives><mixed-citation xml:lang="ru">Demirel §., Erk O., Akkaya V., Tunaci A., Tanakol R., Terzioglu T., §enkal O. Multiple vascular leiomyomas involving bilateral adrenal glands, spleen, and epicardium, associated with bilateral testicular microlithiasis and empty sella turcica. J Pediatr Surg 1997;32(9): 1365-7. doi: 10.1016/s0022-3468(97)90324-9.</mixed-citation><mixed-citation xml:lang="en">Demirel §., Erk O., Akkaya V., Tunaci A., Tanakol R., Terzioglu T., §enkal O. Multiple vascular leiomyomas involving bilateral adrenal glands, spleen, and epicardium, associated with bilateral testicular microlithiasis and empty sella turcica. J Pediatr Surg 1997;32(9): 1365-7. doi: 10.1016/s0022-3468(97)90324-9.</mixed-citation></citation-alternatives></ref><ref id="cit17"><label>17</label><citation-alternatives><mixed-citation xml:lang="ru">Rosenfeld D.L., Girgis W.S., Underberg-Davis S.J. Bilateral smooth-muscle tumors of the adrenals in a child with AIDS. Pediatr Radiol 1999;29(5):376-8. doi: 10.1007/s002470050611.</mixed-citation><mixed-citation xml:lang="en">Rosenfeld D.L., Girgis W.S., Underberg-Davis S.J. Bilateral smooth-muscle tumors of the adrenals in a child with AIDS. Pediatr Radiol 1999;29(5):376-8. doi: 10.1007/s002470050611.</mixed-citation></citation-alternatives></ref><ref id="cit18"><label>18</label><citation-alternatives><mixed-citation xml:lang="ru">Chura J.C., Truskinovsky A.M., Judson P.L., Johnson L., Geller M.A., Downs L.S. Jr. Positron emission tomography and leiomyomas: clinicopathologic analysis of 3 cases of PET scan-positive leiomyomas and literature review. Gynecol Oncol 2007;104(1):247-52. doi: 10.1016/j.ygyno.2006.09.024.</mixed-citation><mixed-citation xml:lang="en">Chura J.C., Truskinovsky A.M., Judson P.L., Johnson L., Geller M.A., Downs L.S. Jr. Positron emission tomography and leiomyomas: clinicopathologic analysis of 3 cases of PET scan-positive leiomyomas and literature review. Gynecol Oncol 2007;104(1):247-52. doi: 10.1016/j.ygyno.2006.09.024.</mixed-citation></citation-alternatives></ref><ref id="cit19"><label>19</label><citation-alternatives><mixed-citation xml:lang="ru">Parelkar S.V., Sampat N.P., Sanghvi B.V., Joshi P.B., Sahoo S.K., Patel J.L., Oak S.N. Case report of bilateral adrenal leiomyoma with review of literature. Pediatr Surg Int 2013;29(6):655-8. doi: 10.1007/s00383-013-3264-1.</mixed-citation><mixed-citation xml:lang="en">Parelkar S.V., Sampat N.P., Sanghvi B.V., Joshi P.B., Sahoo S.K., Patel J.L., Oak S.N. Case report of bilateral adrenal leiomyoma with review of literature. Pediatr Surg Int 2013;29(6):655-8. doi: 10.1007/s00383-013-3264-1.</mixed-citation></citation-alternatives></ref><ref id="cit20"><label>20</label><citation-alternatives><mixed-citation xml:lang="ru">Monforte-Munoz H., Kapoor N., Saavedra J.A. Epstein-Barr virus-associated leiomyomatosis and posttransplant lymphoproliferative disorder in a child with severe combined immunodeficiency: case report and review of the literature. Pediatr Dev Pathol 2003;6(5):449-57. doi: 10.1007/s10024-003-8096-x.</mixed-citation><mixed-citation xml:lang="en">Monforte-Munoz H., Kapoor N., Saavedra J.A. Epstein-Barr virus-associated leiomyomatosis and posttransplant lymphoproliferative disorder in a child with severe combined immunodeficiency: case report and review of the literature. Pediatr Dev Pathol 2003;6(5):449-57. doi: 10.1007/s10024-003-8096-x.</mixed-citation></citation-alternatives></ref><ref id="cit21"><label>21</label><citation-alternatives><mixed-citation xml:lang="ru">Arleo E.K., Schwartz P.E., Hui P., McCarthy S. Review of leiomyoma variants. AJR Am J Roentgenol 2015;205(4):912-21. doi: 10.2214/AJR.14.13946.</mixed-citation><mixed-citation xml:lang="en">Arleo E.K., Schwartz P.E., Hui P., McCarthy S. Review of leiomyoma variants. AJR Am J Roentgenol 2015;205(4):912-21. doi: 10.2214/AJR.14.13946.</mixed-citation></citation-alternatives></ref><ref id="cit22"><label>22</label><citation-alternatives><mixed-citation xml:lang="ru">Kumar S., Nanjappa B., Agrawal P., Pushkarna A. Large bilateral adrenal leiomyomas presenting as calcified adrenal masses: a rare case report. Korean J Urol 2014;55(5):363-6. doi: 10.4111/kju.2014.55.5.363.</mixed-citation><mixed-citation xml:lang="en">Kumar S., Nanjappa B., Agrawal P., Pushkarna A. Large bilateral adrenal leiomyomas presenting as calcified adrenal masses: a rare case report. Korean J Urol 2014;55(5):363-6. doi: 10.4111/kju.2014.55.5.363.</mixed-citation></citation-alternatives></ref><ref id="cit23"><label>23</label><citation-alternatives><mixed-citation xml:lang="ru">Alvarez S., McCabe W.R. Extrapulmonary tuberculosis revisited: a review of experience at Boston City and other hospitals. Medicine (Baltimore) 1984;63(1):25-55. PMID: 6419006.</mixed-citation><mixed-citation xml:lang="en">Alvarez S., McCabe W.R. Extrapulmonary tuberculosis revisited: a review of experience at Boston City and other hospitals. Medicine (Baltimore) 1984;63(1):25-55. PMID: 6419006.</mixed-citation></citation-alternatives></ref><ref id="cit24"><label>24</label><citation-alternatives><mixed-citation xml:lang="ru">Lam K.Y., Lo C.Y. A critical examination of adrenal tuberculosis and a 28-year autopsy experience of active tuberculosis. Clin Endocrinol (Oxf) 2001;54(5):633-9. doi: 10.1046/j.1365-2265.2001.01266.x.</mixed-citation><mixed-citation xml:lang="en">Lam K.Y., Lo C.Y. A critical examination of adrenal tuberculosis and a 28-year autopsy experience of active tuberculosis. Clin Endocrinol (Oxf) 2001;54(5):633-9. doi: 10.1046/j.1365-2265.2001.01266.x.</mixed-citation></citation-alternatives></ref><ref id="cit25"><label>25</label><citation-alternatives><mixed-citation xml:lang="ru">Vinnard C., Blumberg E.A. Endocrine and Metabolic Aspects of Tuberculosis. Microbiol Spectr 2017;5(1). doi: 10.1128/microbiolspec.TNMI7-0035-2016.</mixed-citation><mixed-citation xml:lang="en">Vinnard C., Blumberg E.A. Endocrine and Metabolic Aspects of Tuberculosis. Microbiol Spectr 2017;5(1). doi: 10.1128/microbiolspec.TNMI7-0035-2016.</mixed-citation></citation-alternatives></ref></ref-list><fn-group><fn fn-type="conflict"><p>The authors declare that there are no conflicts of interest present.</p></fn></fn-group></back></article>
