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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="brief-report" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">N.N. Priorov Journal of Traumatology and Orthopedics</journal-id><journal-title-group><journal-title xml:lang="en">N.N. Priorov Journal of Traumatology and Orthopedics</journal-title><trans-title-group xml:lang="ru"><trans-title>Вестник травматологии и ортопедии им. Н.Н. Приорова</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0869-8678</issn><issn publication-format="electronic">2658-6738</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">47740</article-id><article-id pub-id-type="doi">10.17816/vto201522378-83</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Articles</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Статьи</subject></subj-group><subj-group subj-group-type="article-type"><subject>Short Communication</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Idiopathic Multifocal Osteolysis: Case of Surgical Treatment</article-title><trans-title-group xml:lang="ru"><trans-title>Идиопатический мультифокальный остеолиз: случай оперативного лечения</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Pozdeev</surname><given-names>A. P</given-names></name><name xml:lang="ru"><surname>Поздеев</surname><given-names>А. П</given-names></name></name-alternatives><bio xml:lang="ru"><p>доктор мед. наук, профессор, науч. руководитель отделения костной патологии НИДОИ им. Г.И. Турнера»</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zakhar’yan</surname><given-names>E. A</given-names></name><name xml:lang="ru"><surname>Захарьян</surname><given-names>Екатерина Анатольевна</given-names></name></name-alternatives><bio xml:lang="ru"><p>очный аспирант кафедры детской травматологии, ортопедии СЗГМУ им. И.И. Мечникова; Тел.: +7 (911) 095-88-81</p></bio><email>zax-2008@mail.ru</email><xref ref-type="aff" rid="aff2"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Buklaev</surname><given-names>D. S</given-names></name><name xml:lang="ru"><surname>Буклаев</surname><given-names>Д. С</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, зав. отделением артрогрипоза НИДОИ им. Г.И. Турнера</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Krasnogorskiy</surname><given-names>I. N</given-names></name><name xml:lang="ru"><surname>Красногорский</surname><given-names>И. Н</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд. мед. наук, доцент, врач-патологоанатом высшей категории НИДОИ им. Г.И. Турнера</p></bio><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Zubairov</surname><given-names>T. F</given-names></name><name xml:lang="ru"><surname>Зубаиров</surname><given-names>Т. Ф</given-names></name></name-alternatives><bio xml:lang="ru"><p>канд мед. наук, науч. сотр. отделения костной патологии НИДОИ им. Г.И. Турнера</p></bio><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Turner Scientific and Research Institute for Children’s Orthopedics</institution></aff><aff><institution xml:lang="ru">ФГБУ «Научно-исследовательский детский ортопедический институт им. Г.И. Турнера» Минздрава России</institution></aff></aff-alternatives><aff-alternatives id="aff2"><aff><institution xml:lang="en">North-Western State Medical University named after I.I. Mechnikov, St. Petersburg, Russia</institution></aff><aff><institution xml:lang="ru">ГБОУ ВПО «Северо-Западный государственный медицинский университет им. И.И. Мечникова» Минздрава России, Санкт-Петербург, РФ</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2015-09-15" publication-format="electronic"><day>15</day><month>09</month><year>2015</year></pub-date><volume>22</volume><issue>3</issue><issue-title xml:lang="en">NO3 (2015)</issue-title><issue-title xml:lang="ru">ТОМ 22, №3 (2015)</issue-title><fpage>78</fpage><lpage>83</lpage><history><date date-type="received" iso-8601-date="2020-10-20"><day>20</day><month>10</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2015, Eco-Vector</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2015, ООО "Эко-Вектор"</copyright-statement><copyright-year>2015</copyright-year><copyright-holder xml:lang="en">Eco-Vector</copyright-holder><copyright-holder xml:lang="ru">ООО "Эко-Вектор"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/></permissions><self-uri xlink:href="https://journals.eco-vector.com/0869-8678/article/view/47740">https://journals.eco-vector.com/0869-8678/article/view/47740</self-uri><abstract xml:lang="en"><p>Idiopathic osteolysis is a rare disorder characterized by spontaneous, massive and progressive resorption of bone tissue. Massive osteolysis results from proliferation of blood and lymphatic vessels with thin walls, resembling capillaries, in the bone and surrounding soft tissues. Literature review on this problem and clinical case of a patient successfully operated on using the technique elaborated at our clinic are presented. Surgical interventions enabled to achieve the restoration of tubular bones integrity and ensured conditions for independent patient’s movement. Possibility of the performance of reconstructive surgical interventions for the restoration of limb weight bearing ability that is reasonable to combine with bisphosphonate therapy.</p></abstract><trans-abstract xml:lang="ru"><p>Идиопатический остеолиз - редко встречающееся патологическое состояние, характеризующееся спонтанной, массивной и прогрессирующей резорбцией костной ткани. Массивный остеолиз является результатом пролиферации в костной и окружающих мягких тканях тонкостенных кровеносных и лимфатических сосудов, напоминающих капилляры. В статье представлены обзор литературы по данной проблеме и описание клинического наблюдения пациентки, успешно прооперированной с использованием разработанной в клинике методики. Выполненные вмешательства позволили добиться восстановления целостности трубчатых костей и обеспечили условия для самостоятельного передвижения. Продемонстрирована возможность проведения реконструктивных оперативных вмешательств с целью восстановления опороспособности конечностей, которые целесообразно сочетать с терапией бисфосфонатами.</p></trans-abstract><kwd-group xml:lang="en"><kwd>essential osteolysis</kwd><kwd>Gorham’s disease</kwd><kwd>pseudarthrosis</kwd><kwd>bone plastic operations</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>остеолиз</kwd><kwd>синдром Горхема</kwd><kwd>ложные суставы</kwd><kwd>костнопластические операции</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>1. Baba A.N., Bhat Y.J., Paljor S.D., Nazir A., Khan N.A. Gorham's disease of femur. Indian J. Orthop. 2011; 45 (6): 565-8.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>2. Оттева Э.Н., Кочерова Т.Ю., Шепичев Е.В. Синдром Горхема - Стоута: описания случая. Научно-практическая ревматология. 2010; 4: 83-6.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Liu Y., Zhong D.R., Zhou P.R., Lv F., Ma D.D., Xia W.B. et al. Gorham-Stout disease: radiological, histological, and clinical features of 12 cases and review of literature. Clin. Rheumatol. 2014; Sep 18.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>4. Torg J.S., DiGeorge A.M., Kirkpatrick J.A. Jr., et al. Hereditary multicentric osteolysis with recessive transmission: a new syndrome. J. Pediatr. 1969; 75: 243-52.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>5. Ozbayrak M., Yilmaz M.H., Kantarci F., Ozer H., Harmanci K., Babacan M., Dervisoglu S. A case of an idiopathic massive osteolysis with skip lesions. Korean J. Radiol. 2013; 14 (6): 946-50.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>6. Kilicoglu Z.G., Kizildemir Kis. N., Vardar Aker F., Berkman M.Z., Simsek M.M. Gorham disease of the craniocervical junction: X-ray, computed tomography, and magnetic resonance imaging findings. Spine J. 2013; 13 (5): e11-4.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>7. Pazzaglia U.E., Andrini L., Bonato M., Leuther M. Pathology of disappearing bone disease: a case report with immunohistochemical study. Int. Orthop. 1997; 121: 303-7.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Goldfarb C.A., Steffen J.A., Whyte M.P. Idiopathic multicentric osteolysis: upper extremity manifestations and surgical considerations during childhood. J. Hand Surg. Am. 2012; 37 (8): 1677-83.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>9. Gowin W., Rahmanzadeh R. Radiologic diagnosis of massive idiopathic osteolysis (Gorham-Stout Syndrome). Rontgenpraxis. 1985; 38: 128-34</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>10. Johnson P.M., McClure J.G. Observations of massive osteolysis: a review of the literature and report of a case. Radiology. 1958; 71: 28-42.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>11. Möller G., Priemel M., Amling M., Werner M., Kuhlmey A.S., Delling G. The Gorham-Stout syndrome (Gorham’s massive osteolysis). A report of six cases with histopathological findings. J. Bone Joint Surg. Br. 1999; 81 (3): 501-6.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Scheller K., Herrmann-Trost P., Diesel L., Busse C., Heinzelmann C. Unspecific, idiopathic isolated osteolysis (Gorham-Stout syndrome) of the mandibular condylar process with its radiological, histological and clinical features: a case report and review of literature. Oral Maxillofac Surg. 2014; 18 (1): 75-9.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Knoch H.-G. Die Gorhamsche Krankheit aus klinischer Sicht. Zentralbl Chir. 1963; 18: 674-83.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>14. Young J.W., Galbraith M., Cunningham J., Roof B.S., Vujic I., Gobien R.P. et al. Progressive vertebral collapse in diffuse angiomatosis. Metab. Bone Dis. Relat. Res. 1983; 5 (2): 53-60.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>15. Heyden G., Kindblom L.-G., Nielsen J.M. Disappearing bone disease: a clinical and histological study. J. Bone Joint Surg. Am. 1977; 59 (1): 57-61.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>16. Spieth M.E., Greenspan A., Forrester D.M., Ansari A.N., Kimura R.L., Gleason-Jordan I. Gorham,s disease of the radius: radiographic, scintigraphic, and MRI findings with pathological correlation: a case report and review of the literature. Skeletal. Radiol. 1997; 26: 659-63.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>17. Devlin R.D., Bone H.G., Roodman G.D. Interleukin-6: a potential mediator of the massive osteolysis in patients with Gorham-Stout disease. J. Clin. Endocrinol. Metab. 1996; 81: 1893-97.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>18. Hardegger F., Simpson L.A., Segmueller G. The syndrome of idiopathic osteolysis: classification, review and case report. J. Bone Joint Surg. Br. 1985; 67: 89-93.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Garbers E., Reuther F., Delling G. Report of a rare case of gorham-stout disease of both shoulders: bisphosphonate treatment and shoulder replacement. Case Rep. Rheumatol. 2011; 2011: 565142.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>20. Buerfeind A., Bürger H., Schlüter-Brust K., Eysel P., Delank K.S. Gorham-Stout syndrome (GSS) with fulminant aseptic osteonecrosis of the shoulder. Orthopade. 2010; 39 (10): 1003-8.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>21. Deveci M., Inan N., Corapçıoğlu F., Ekingen G. Gorham-Stout syndrome with chylothorax in a six-year-old boy. Indian J. Pediatr. 2011; 78 (6): 737-9.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Heyd R., Rabeneck D., Dörnenburg O., Tselis N., Zamboglou N. Gorham-Stout syndrome of the pelvic girdle treated by radiation therapy: a case report. Strahlenther Onkol. 2011; 187 (2): 140-3.</mixed-citation></ref></ref-list></back></article>
