<?xml version="1.0" encoding="UTF-8"?>
<!DOCTYPE root>
<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="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Terapevticheskii arkhiv</journal-id><journal-title-group><journal-title xml:lang="en">Terapevticheskii arkhiv</journal-title><trans-title-group xml:lang="ru"><trans-title>Терапевтический архив</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0040-3660</issn><issn publication-format="electronic">2309-5342</issn><publisher><publisher-name xml:lang="en">LLC Obyedinennaya Redaktsiya</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">31567</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Editorial article</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Передовая статья</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Secondary dysmyelopoiesis in patients with myelodysplastic syndromes: A review of literature and the authors' data</article-title><trans-title-group xml:lang="ru"><trans-title>Вторичный дисмиелопоэз у больных миелодиспластическими синдромами</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Dvirnyk</surname><given-names>V N</given-names></name><name xml:lang="ru"><surname>Двирнык</surname><given-names>В Н</given-names></name></name-alternatives><email>dvirnyk.v@blood.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kokhno</surname><given-names>A V</given-names></name><name xml:lang="ru"><surname>Кохно</surname><given-names>А В</given-names></name></name-alternatives><email>anilako@rambler.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Parovichnikova</surname><given-names>E N</given-names></name><name xml:lang="ru"><surname>Паровичникова</surname><given-names>Е Н</given-names></name></name-alternatives><email>elenap@blood.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en"></institution></aff><aff><institution xml:lang="ru">ФГБУ "Гематологический научный центр" Минздрава России, Москва</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2014-07-15" publication-format="electronic"><day>15</day><month>07</month><year>2014</year></pub-date><volume>86</volume><issue>7</issue><issue-title xml:lang="en">VOL 86, NO7 ()</issue-title><issue-title xml:lang="ru">ТОМ 86, №7 (2014)</issue-title><fpage>97</fpage><lpage>103</lpage><history><date date-type="received" iso-8601-date="2020-04-10"><day>10</day><month>04</month><year>2020</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2014, Consilium Medicum</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2014, ООО "Консилиум Медикум"</copyright-statement><copyright-year>2014</copyright-year><copyright-holder xml:lang="en">Consilium Medicum</copyright-holder><copyright-holder xml:lang="ru">ООО "Консилиум Медикум"</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">https://creativecommons.org/licenses/by-nc-sa/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://ter-arkhiv.ru/0040-3660/article/view/31567">https://ter-arkhiv.ru/0040-3660/article/view/31567</self-uri><abstract xml:lang="en"><p>To interpret hematopoietic cell myelodysplastic changes found during the primary diagnosis of myelodysplastic syndromes or other diseases and during therapy is an enormously complex clinical and laboratory problem. In what cases do these changes serve as a manifestation of clonal disease and in what cases are these changes a result of various effects? Alimentary, toxic factors, infectious agents, and iatrogenic effects may cause myelodysplastic signs in the hematopoietic cells. This review depicts diverse hematopoietic cell dysplastic changes that can be observed as a result of the effects of one drug or another, toxic factors, and infectious agents.</p></abstract><trans-abstract xml:lang="ru"><p>Аннотация. Трактовка миелодиспластических изменений кроветворных клеток, обнаруженных при первичной диагностике миелодиспластических синдромов или других заболеваний и в процессе терапии, является исключительно сложной клинико-лабораторной задачей. В каких случаях эти изменения служат проявлением клонального заболевания, а в каких - следствием разнообразных воздействий? Алиментарные, токсичные факторы, инфекционные агенты, а также ятрогенные воздействия могут быть причиной появления миелодиспластических признаков в кроветворных клетках. В настоящем обзоре описаны разнообразные диспластические изменения кроветворных клеток, которые можно наблюдать как результат влияния тех или иных лекарственных препаратов, токсичных факторов, инфекционных агентов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>myelodysplastic syndrome</kwd><kwd>secondary myelodysplasia</kwd><kwd>hematopoietic cell morphology</kwd><kwd>iatrogenic effect</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>миелодиспластический синдром</kwd><kwd>вторичная миелодисплазия</kwd><kwd>морфология кроветворных клеток</kwd><kwd>ятрогенные воздействия</kwd></kwd-group></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><mixed-citation>Swerdlow S.H. Campo E., Harris N.L. et al. WHO Classification of Tumors of Haematopoietic and Lymphoid Tissues. Lyon: IARS-press 2008; 439.</mixed-citation></ref><ref id="B2"><label>2.</label><mixed-citation>Schmitz L.L., McClure J.S., Litz C.E. et al. Morphologic and quantitave changes in blood and marrow cells following growth factor therapy. Am О Сlin Pathol 1994; 101: 67-75.</mixed-citation></ref><ref id="B3"><label>3.</label><mixed-citation>Scott J.M., Weir D.G. Drug-induced megaloblastic change. Clin Haematol 1980; 9 (3): 587-606.</mixed-citation></ref><ref id="B4"><label>4.</label><mixed-citation>Lindenbaum J. Drugs and vitamin B12 and folate metabolism. Curr Concepts Nutr 1983; 12: 73-87.</mixed-citation></ref><ref id="B5"><label>5.</label><mixed-citation>Bielenberg J. Folic acid and vitamin deficiency caused by oral contraceptives. Med Monatsschr Pharm 1991; 14 (8): 244-247.</mixed-citation></ref><ref id="B6"><label>6.</label><mixed-citation>Piso R.J., Kriz K., Desax M.-C. Severe isoniazid related sideroblastic anemia. Hematol Rep 2011; 3 (1): 3-4.</mixed-citation></ref><ref id="B7"><label>7.</label><mixed-citation>Sharp R.A., Lowe J.G., Johnston R.N. Antituberculous drugs and sideroblastic anaemia. Br J Clin Pract 1990; 44: 706-707.</mixed-citation></ref><ref id="B8"><label>8.</label><mixed-citation>Yoshimoto S., Takeuchi M., Tada A. Secondary sideroblastic anemia caused by long term administration of anti-tuberculous agents including isoniazid]. Rinsho Ketsueki 1992; 33: 986-990.</mixed-citation></ref><ref id="B9"><label>9.</label><mixed-citation>Girdwood R.H. Drug-induced anaemias. Drugs 1976; 11 (5): 394-404.</mixed-citation></ref><ref id="B10"><label>10.</label><mixed-citation>Gregg K.T., Reddy V., Prchal J.T. Cooper deficiency masquerading as myelodysplastic syndrome. Blood 2002; 100 (4): 1493-1495.</mixed-citation></ref><ref id="B11"><label>11.</label><mixed-citation>Huff J.D., Keung Y.K., Thakuri M. et al. Am J Hematol 2007; 82 (7): 625-630.</mixed-citation></ref><ref id="B12"><label>12.</label><mixed-citation>Heidemann E., Nerke O., Waller H.D. Alcohol induced changes in hemopoiesis. Klin Wochenschr 1981; 59 (23): 1303-1312.</mixed-citation></ref><ref id="B13"><label>13.</label><mixed-citation>Casagrande G., Michot F. Alcohol-induced bone marrow damage: status before and after a 4-week period of abstinence from alcohol with or without disulfiram. A randomized bone marrow study in alcohol-dependent individuals. Blut 1989; 59 (3): 231-236.</mixed-citation></ref><ref id="B14"><label>14.</label><mixed-citation>Hellerich U., Budde R. Toxic alcohol dysmyelopoiesis - bone marrow histology studies of a forensic medicine autopsy sample. Beitr Gerichtl Med 1992; 50: 69-74.</mixed-citation></ref><ref id="B15"><label>15.</label><mixed-citation>Latvala J., Parkkila S., Niemelä O. Excess alcohol consumption is common in patients with cytopenia: studies in blood and bone marrow cells. Alcohol Clin Exp Res 2004; 28 (4): 619-624.</mixed-citation></ref><ref id="B16"><label>16.</label><mixed-citation>Niemelä O., Parkkila S. Alcoholic macrocytosis - is there a role for acetaldehyde and adducts? Addict Biol 2004; 9 (1): 3-10.</mixed-citation></ref><ref id="B17"><label>17.</label><mixed-citation>Hoffmann K., Dreger C.K., Olins A.L. et al. Mutations in the gene encoding the lamin B receptor produce an altered nuclear morphology in granulocytes (Pelger-Huёt anomaly). Nat Genet 2002; 31: 410-414.</mixed-citation></ref><ref id="B18"><label>18.</label><mixed-citation>Pelger K. Demonstrate van een paar zeldzaam voorkomende typen van bloedlichaampjes en bespreking der patienten. Ned Tijdschr Geneeskd 1928; 72: 1178.</mixed-citation></ref><ref id="B19"><label>19.</label><mixed-citation>Huёt G.J. Familiaire anomalie der leucocyten. Ned Tijdschr Geneeskd 1931; 75: 5956-5959.</mixed-citation></ref><ref id="B20"><label>20.</label><mixed-citation>Speeckaert M.M., Verhelst C., Koch A. et al. Pelger-Huёt anomaly: a critical review of the literature. Acta Haematol 2009; 121: 202-206.</mixed-citation></ref><ref id="B21"><label>21.</label><mixed-citation>Cunningham J.M., Patnaik M.M., Hammerschmidt D.E. et al. Historical perspective and clinical implications of the Pelger-Hьet cell. Am J Hematol 2009; 84: 116-119.</mixed-citation></ref><ref id="B22"><label>22.</label><mixed-citation>Cunningham I., MacCallum S.J., Nicholls M.D. et al. The myelodysplastic syndromes: an analysis of prognostic factors in 226 cases from a single institution. Br J Haematol 1995; 90: 602-606.</mixed-citation></ref><ref id="B23"><label>23.</label><mixed-citation>Kuriyama K., Tomonaga M., Matsuo T. et al. Diagnostic significance of detecting pseudo-Pelger-Huёt anomalies and micro-megakaryocytes in myelodysplastic syndrome. Br J Haematol 1986; 63: 665-669.</mixed-citation></ref><ref id="B24"><label>24.</label><mixed-citation>Germing U., Strupp C., Giagounidis A. Detalied morphologic finding in 2773 patients with myelodysplastic syndromes. Leuk Res 2009; 33: 34.</mixed-citation></ref><ref id="B25"><label>25.</label><mixed-citation>Juneja S.K., Matthews J.P., Luzinat R. et al. Association of acquired Pelger-Huёt anomaly with taxoid therapy. Br J Haematol 1996; 93: 139-141.</mixed-citation></ref><ref id="B26"><label>26.</label><mixed-citation>Teshima T., Shibuya T., Harada M. et al. Effects of G-CSF, GM-CSF, and IL-5 on nuclear segmentation of neutrophils and eosinophils in congenital or acquired Pelger-Huёt anomaly. Exp Hematol 1991; 19: 322-325.</mixed-citation></ref><ref id="B27"><label>27.</label><mixed-citation>Moreira A.M., Vieira L.M., Rios D.R. et al. Acquired Pelger-Huёt anomaly associated with ibuprofen therapy [letter] [published correction appears in Clin Chim Acta. 2010; 411: 1397]. Clin Chim Acta 2009; 409: 140-141.</mixed-citation></ref><ref id="B28"><label>28.</label><mixed-citation>Kaplan J.M., Barrett O. Jr. Reversible pseudo-Pelger anomaly related to sulfisoxazole therapy. N Engl J Med 1967; 277: 421-422.</mixed-citation></ref><ref id="B29"><label>29.</label><mixed-citation>Levin J.M. Pelger-Huёt anomaly and d-penicillamine [letter]. J Rheumatol 1980; 7: 418-419.</mixed-citation></ref><ref id="B30"><label>30.</label><mixed-citation>Wang E., Boswell E., Siddiqi I. et al. Pseudo-Pelger-Huёt Anomaly Induced by Medications. A Clinicopathologic Study in Comparison With Myelodysplastic Syndrome-Related Pseudo-Pelger-Huёt Anomaly. Am J Clin Pathol 2011; 135: 291-303.</mixed-citation></ref><ref id="B31"><label>31.</label><mixed-citation>Etzell J.E., Wang E. Acquired Pelger-Huёt anomaly in association with concomitant tacrolimus and mycophenolate mofetil in a liver transplant patient: a case report and review of the literature. Arch Pathol Lab Med 2006; 130: 93-96.</mixed-citation></ref><ref id="B32"><label>32.</label><mixed-citation>Asmis L.M., Hadaya K., Majno P. et al. Acquired and reversible Pelger-Huёt anomaly of polymorphonuclear neutrophils in three transplant patients receiving mycophenolate mofetil therapy. Am J Hematol 2003; 73: 244-248.</mixed-citation></ref><ref id="B33"><label>33.</label><mixed-citation>Kennedy G.A., Kay T.D., Johnson D.W. et al. Neutrophil dysplasia characterised by a pseudo-Pelger-Huёt anomaly occurring with the use of mycophenolate mofetil and ganciclovir following renal transplantation: a report of five cases. Pathology 2002; 34: 263-266.</mixed-citation></ref><ref id="B34"><label>34.</label><mixed-citation>Gondo H., Okamura C., Osaki K. et al. Acquired Pelger-Huёt anomaly in association with concomitant tacrolimus and fluconazole therapy following allogeneic bone marrow transplantation. Bone Marrow Transplant 2000; 26: 1255-1257.</mixed-citation></ref><ref id="B35"><label>35.</label><mixed-citation>Taegtmeyer A., Halil O., Bell A. et al. Neutrophil dysplasia (acquired pseudo-pelger anomaly) caused by ganciclovir. Transplantation 2005; 80 (1): 127-130.</mixed-citation></ref><ref id="B36"><label>36.</label><mixed-citation>Gondo H., Okamura C., Osaki K. et al. Acquired Pelger-Huёt anomaly in association with concomitant tacrolimus and fluconazole therapy following allogeneic bone marrow transplantation. Bone Marrow Transplant 2000; 26: 1255-1257.</mixed-citation></ref><ref id="B37"><label>37.</label><mixed-citation>Teshima T., Shibuya T., Harada M. et al. Effects of G-CSF, GM-CSF, and IL-5 on nuclear segmentation of neutrophils and eosinophils in congenital or acquired Pelger-Huёt anomaly. Exp Hematol 1991; 19: 322-325.</mixed-citation></ref><ref id="B38"><label>38.</label><mixed-citation>Cicchitto G., Parravicini M., De Lorenzo S. et al. Tuberculosis and Pelger-Huёt anomaly: case report. Panminerva Med 1999; 41: 367-369.</mixed-citation></ref><ref id="B39"><label>39.</label><mixed-citation>Rosell Arnold E., Rodrіguez Miguélez J.M., Roquer González J.M. et al. Reversible Pelger-Huёt anomaly associated with acute gastroenteritis caused by salmonella group D [in Spanish]. An Esp Pediatr 1989; 30: 143-144.</mixed-citation></ref><ref id="B40"><label>40.</label><mixed-citation>van Hook L., Spivack C., Duncanson F.P. Acquired Pelger-Huёt anomaly associated with Mycoplasma pneumoniae pneumonia. Am J Clin Pathol 1985; 84: 248-251.</mixed-citation></ref><ref id="B41"><label>41.</label><mixed-citation>Speeckaert M.M., Verhelst C., Koch A. et al. Pelger-Huёt anomaly: a critical review of the literature. Acta Haematol 2009; 21: 202-205.</mixed-citation></ref><ref id="B42"><label>42.</label><mixed-citation>Рудницкая Ю.В., Морозова Е.В., Мамаев Н.Н. и др. Аллогенная трансплантация гемопоэтических стволовых клеток крови с использованием режимов кондиционирования со сниженной интенсивностью у пациентов с миелодиспластическим синдромом. Клин онкогематол 2011; 3: 196-200.</mixed-citation></ref><ref id="B43"><label>43.</label><mixed-citation>Wang E., Boswell E., Siddiqi I. et al. Pseudo-Pelger-Huёt Anomaly Induced by Medications. A Clinicopathologic Study in Comparison With Myelodysplastic Syndrome-Related Pseudo-Pelger-Huёt Anomaly. Am J Clin Pathol 2011; 135: 291-303.</mixed-citation></ref><ref id="B44"><label>44.</label><mixed-citation>Клясова Г.А. Профилактика и лечение инфекционных осложнений. Руководство по гематологии. Под ред. А.И. Воробьева. М 2007: 465-486.</mixed-citation></ref><ref id="B45"><label>45.</label><mixed-citation>Miyahara M., Shimamoto Y., Yamada H. et al. Cytomegalovirus-associated myelodysplasia and thrombocytopenia in an immunocompetent adult. Ann Hematol 1997; 74 (2): 99-101.</mixed-citation></ref><ref id="B46"><label>46.</label><mixed-citation>Mizutani K., Azuma E., Komada Y. et al. An infantile case of cytomegalovirus induced idiopathic thrombocytopenic purpura with predominant proliferation of CD10 positive lymphoblast in bone marrow. Acta Paediatr Jpn 1995; 37 (1): 71-74.</mixed-citation></ref><ref id="B47"><label>47.</label><mixed-citation>Гармаева Т.Ц., Куликов С.М., Карякин А.В. и др. Мониторирование факторов риска и индикаторов инфицированности вирусами гепатитов В и С гематологических больных. Гематол и трансфузиол 2006; 1: 23-27.</mixed-citation></ref><ref id="B48"><label>48.</label><mixed-citation>Февралева И.С., Глинщикова О.А., Элижбаева М.А. и др. Распространенность парвовируса В19 среди больных гематологического стационара. Гематол и трансфузиол 2011; 6: 24-28.</mixed-citation></ref><ref id="B49"><label>49.</label><mixed-citation>Гайдамака Н.В., Паровичникова Е.Н., Завалишина Л.Э. и др. Длительные аплазии костного мозга после химиотерапии у больных острыми лейкозами. Тер арх 2010; 7: 12-18.</mixed-citation></ref><ref id="B50"><label>50.</label><mixed-citation>Heegaard E.D., Brown K.E. Human parvovirus B19. Clin Microbiol Rev 2002; 15: 485-505.</mixed-citation></ref><ref id="B51"><label>51.</label><mixed-citation>Slavov S.N., Kashima S., Pinto A.C., Covas D.T. Human parvovirus B19: general considerations and impact on patients with sickle-cell disease and thalassemia and on blood transfusions. FEMS Immunol Med Microbiol 2011; 3 (62): 247-262.</mixed-citation></ref><ref id="B52"><label>52.</label><mixed-citation>Carpenter S.L., Zimmerman S.A., Ware R.E. Acute parvovirus B19 infection mimicking congenital dyserythropoietic anemia. J Pediatr Hematol Oncol 2004; 26: 133-135.</mixed-citation></ref><ref id="B53"><label>53.</label><mixed-citation>Weiland H.T., Salimans M.M., Fibbe W.E. et al. Prolonged parvovirus B19 infection with severe anaemia in a bone marrow transplant patient. Br J Haematol 1989; 71: 300.</mixed-citation></ref><ref id="B54"><label>54.</label><mixed-citation>Solano C., Juan O., Gimeno C., Garcia-Conde J. Engraftment failure associated with peripheral blood stem cell transplantation after B19 parvovirus infection. Blood 1996; 88: 1515-1517.</mixed-citation></ref><ref id="B55"><label>55.</label><mixed-citation>Azzi A., Fanci R., Ciappi S. et al. Human parvovirus B19 infection in bone marrow transplantation patients. Am J Hematol 1993; 44: 207-209.</mixed-citation></ref><ref id="B56"><label>56.</label><mixed-citation>Broliden K. Parvovirus B19 infection in pediatric solid-organ and bone marrow transplantation. Pediatr Transplant 2001; 5: 320-330.</mixed-citation></ref><ref id="B57"><label>57.</label><mixed-citation>Frickhofen N., Arnold R., Hertenstein B. et al. Parvovirus B19 infection and bone marrow transplantation. Ann Hematol 1992; 64 (Suppl): A121-124.</mixed-citation></ref><ref id="B58"><label>58.</label><mixed-citation>Niitsu H., Takatsu H., Miura I. et al. Pure red cell aplasia induced by B19 parvovirus during allogeneic bone marrow transplantation. Rinsho Ketsueki 1990; 31: 1566-1571.</mixed-citation></ref><ref id="B59"><label>59.</label><mixed-citation>Гармаева Т.Ц. Вирусные гепатиты В и С у больных заболеваниями системы крови: Автореф. дис. ... д-ра мед. наук. М 2012; 46.</mixed-citation></ref><ref id="B60"><label>60.</label><mixed-citation>Савченко В.Г., Троицкая В.В., Мисюрин А.В. и др. Цитомегаловирусная инфекция у пациентов с гемобластозами Тер арх 2003; 7: 52-58.</mixed-citation></ref><ref id="B61"><label>61.</label><mixed-citation>Miyahara M., Shimamoto Y., Yamada H. Cytomegalovirus-associated myelodysplasia and thrombocytopenia in an immunocompetent adult. Ann Hematol 1997; 74 (2): 99-101.</mixed-citation></ref><ref id="B62"><label>62.</label><mixed-citation>Bain B.J. The haematological features of HIV infection. Br J Haematol 1997; 99: 1-8.</mixed-citation></ref><ref id="B63"><label>63.</label><mixed-citation>Pande А., Bhattacharyya M., Pain S. Study of bone marrow changes in antiretroviral naive human immunodeficiency virus-infected anemic patients. Indian J Pathol Microbiol 2011; 54 (3): 542-546.</mixed-citation></ref><ref id="B64"><label>64.</label><mixed-citation>Kopterides P., Halikias S., Tsavaris N. Visceral leishmaniasis masquerading as myelodysplasia. Am J Hematol 2003; 74: 198-199.</mixed-citation></ref><ref id="B65"><label>65.</label><mixed-citation>Клясова Г.А. Рациональное лечение инфекционных осложнений цитостатической терапии в условиях иммуносупрессии. Вестн Московского онкологического общества 2009; 1: 5-8.</mixed-citation></ref><ref id="B66"><label>66.</label><mixed-citation>Bernstein W.B., Trotta R.F., Rector J.T. et al. Mechanisms for linezolid-induced anemia and thrombocytopenia. Ann Pharmacother 2003; 37 (4): 517-520.</mixed-citation></ref><ref id="B67"><label>67.</label><mixed-citation>Gerson S.L., Kaplan S.L., Bruss J.B. et al. Hematologic Effects of Linezolid: Summary of Clinical Experience. Antimicrob Agents Chemother. 2002; 46 (8): 2723-2726.</mixed-citation></ref><ref id="B68"><label>68.</label><mixed-citation>Farber B.F., Moellering R.C. Retrospective Study of the Toxicity of Preparations of Vancomycin from 1974 to 1981. Antimicrob Agents Chemother 1983; 23 (1): 138-141.</mixed-citation></ref><ref id="B69"><label>69.</label><mixed-citation>Rao N., Ziran B.H., Wagener M.M. et al. Similar Hematologic Effects of Long-Term Linezolid and Vancomycin Therapy in a Prospective Observational Study of Patients with Orthopedic Infections. Clin Infect Dis 2004; 38 (8): 1058-1064.</mixed-citation></ref><ref id="B70"><label>70.</label><mixed-citation>Rouveix B., Lassoued K., Vittecoq D., Regnier B. Neutropenia due to beta lactamine antibodies. Br Med J (Clin Res Ed) 1983; 287 (6408): 1832-1834.</mixed-citation></ref><ref id="B71"><label>71.</label><mixed-citation>Bernstein L.S. Adverse reactions to trimethoprim-sulfamethoxazole, with particular reference to long-term therapy. Can Med Assoc J 1975; 112 (13 Spec No): 96-98.</mixed-citation></ref><ref id="B72"><label>72.</label><mixed-citation>Jewkes R.F., Edwards M.S., Grant B.J. Haematological changes in a patient on long-term treatment with a trimethoprim-sulphonamide combination. Postgrad Med J 1970; 46 (542): 723-726.</mixed-citation></ref><ref id="B73"><label>73.</label><mixed-citation>Parmentier S., Schetelig J., Lorenz K. et al. Assessment of dysplastic hematopoiesis: lessons from healthy bone marrow donors. Hematologica 2012; 97 (5): 723-730.</mixed-citation></ref><ref id="B74"><label>74.</label><mixed-citation>Куликов С.М., Гармаева Т.Ц., Зингерман Б.В. и др. Вирусная безопасность гемотрансфузий и методы ее оценки. Гематол и трансфузиол 2008; 4: 3-5.</mixed-citation></ref><ref id="B75"><label>75.</label><mixed-citation>Троицкая В.В. Диагностика и лечение цитомегаловирусной инфекции у больных гемобластозами: Автореф. дис. ... канд. мед. наук. М 2004.</mixed-citation></ref><ref id="B76"><label>76.</label><mixed-citation>Lee S.H., Erber W.N., Porwit A. et al. ICSH guidelines for the standardization of bone marrow specimens and reports. Int J Lab Hematol 2008; 30 (5): 349-364.</mixed-citation></ref><ref id="B77"><label>77.</label><mixed-citation>Bain B.J. Blood cells: a practical guide. 4th ed. Malden, Mass: Blackwell 2006.</mixed-citation></ref></ref-list></back></article>
