Справка
x
Поиск
Закладки
Озвучить книгу
Изменить режим чтения
Изменить размер шрифта
Оглавление
Для озвучивания и цитирования книги перейдите в режим постраничного просмотра.
Приобретенная чистая красноклеточная аплазия (эритробластопения)
Список литературы
Поставить закладку
Means R.T. Pure red cell aplasia // Blood. 2016. Vol. 128, № 21.
Means R.T. Pure red cell aplasia: The second hundred years // American Journal of the Medical Sciences. 2023. Vol. 366, № 3.
Narla A., Lipton J.M., Means R.T. Red cell aplasia: Acquired and congenital disorders // Wintrobe’s Clinical Hematology: Fourteenth Edition. 2018.
Ruggero D., Shimamura A. Marrow failure: A window into ribosome biology // Blood. 2014. Vol. 124, № 18.
Frickhofen N. et al. Parvovirus B19 as a cause of acquired chronic pure red cell aplasia // Br J Haematol. 1994. Vol. 87, № 4.
Brown K.E. et al. Resistance to Parvovirus B19 Infection Due to Lack of Virus Receptor (Erythrocyte P Antigen) // New England Journal of Medicine. 1994. Vol. 330, № 17.
Жукова Л.Ю. Х.А.В., К.О.Л., С.Н.Е., Т.А.Н. Транзиторная эритробластопения детского возраста: обзор 39 случаев // Педиатр. 2015. Vol. 6, № 15. P. 44–53.
Sawada K., Fujishima N., Hirokawa M. Acquired pure red cell aplasia: Updated review of treatment // British Journal of Haematology. 2008. Vol. 142, № 4.
Gurnari C., Maciejewski J.P. How I manage acquired pure red cell aplasia in adults // Blood. 2021. Vol. 137, № 15.
Lobbes H. et al. Pure red cell aplasia in systemic lupus erythematosus, a nationwide retrospective cohort and review of the literature // Rheumatology (United Kingdom). 2022. Vol. 61, № 1.
Aung F.M. et al. Incidence and natural history of pure red cell aplasia in major ABO-mismatched haematopoietic cell transplantation // Br J Haematol. 2013. Vol. 160, № 6.
Masuda M. et al. Clonal T cells of pure red-cell aplasia // Am J Hematol. 2005. Vol. 79, № 4.
Visco C. et al. Autoimmune cytopenias in chronic lymphocytic leukemia // American Journal of Hematology. 2014. Vol. 89, № 11.
Fujishima N. et al. Long-term responses and outcomes following immunosuppressive therapy in large granular lymphocyte leukemia-associated pure red cell aplasia: A Nationwide Cohort Study in Japan for the PRCA Collaborative Study Group // Haematologica. 2008. Vol. 93, № 10.
Mijovic A. et al. Chronic myeloid leukemia associated with pure red cell aplasia and terminating in promyelocytic transformation // Am J Hematol. 1989. Vol. 31, № 2.
Bernard C. et al. Thymoma associated with autoimmune diseases: 85 cases and literature review // Autoimmunity Reviews. 2016. Vol. 15, № 1.
Carson K.R. et al. Clinical characteristics of erythropoietin-associated pure red cell aplasia // Best Practice and Research: Clinical Haematology. 2005. Vol. 18, № 3 SPEC. ISS.
Choudry M.A., Moffett B.K., Laber D.A. Pure red-cell aplasia secondary to pregnancy, characterization of a syndrome // Ann Hematol. 2007. Vol. 86, № 4.
Nakazawa H. et al. Incidence of acquired pure red cell aplasia: a nationwide epidemiologic analysis with 2 registry databases in Japan // Blood Adv. 2022. Vol. 6, № 24.
Balasubramanian S.K. et al. Rational management approach to pure red cell aplasia // Haematologica. 2018. Vol. 103, № 2.
Masaoka A. et al. Thymomas associated with pure red cell aplasia. Histologic and follow‐up studies // Cancer. 1989. Vol. 64, № 9.
Seifi S. et al. Thymoma recurrence and its predisposing factors in Iranian population: A single center study // Tanaffos. 2019. Vol. 18, № 4.
Hishida T. et al. Clinical features and prognostic impact of coexisting autoimmune disease other than myasthenia gravis in resected thymomas: Analysis of a Japanese multi-institutional retrospective database // European Journal of Cardio-thoracic Surgery. 2021. Vol. 59, № 3.
Maggi G. et al. Thymoma: Results of 241 operated cases // The Annals of Thoracic Surgery. 1991. Vol. 51, № 1.
Qiu Z.Y. et al. Methotrexate therapy of T-cell large granular lymphocytic leukemia impact of STAT3 mutation // Oncotarget. 2016. Vol. 7, № 38.
Kawahara S. et al. Clinical analysis of 52 patients with granular lymphocyte proliferative disorder (GLPD) showed frequent anemia in indolent T-cell GLPD in Japan // Eur J Haematol. 2009. Vol. 82, № 4.
Kwong Y.L. et al. T-cell large granular lymphocyte leukemia: An Asian perspective // Annals of Hematology. 2010. Vol. 89, № 4.
Hampel P.J. et al. Autoimmune cytopenias in patients with chronic lymphocytic leukaemia treated with ibrutinib in routine clinical practice at an academic medical centre // Br J Haematol. 2018. Vol. 183, № 3.
Tsang M. et al. Pure Red Cell Aplasia (PRCA) in Chronic Lymphocytic Leukemia (CLL): Etiology, Therapy, and Outcomes // Blood. 2015. Vol. 126, № 23.
Longval T. et al. Treatment for pure red cell aplasia after major ABO-incompatible allogeneic stem cell transplantation: a multicentre study // Br J Haematol. 2021. Vol. 193, № 4.
World Health Organization. ICD-10: international statistical classification of diseases and related health problems: tenth revision. 2nd ed. Geneva PP - Geneva: World Health Organization.
Petrenko A.A. et al. Pure red cell aplasia of the bone marrow in combination with thymoma. A literature review and own data // Ter Arkh. 2019. Vol. 91, № 7.
Shimizu R. et al. Efficacy and safety of oral deferasirox treatment for transfusional iron overload in pure red cell aplasia patients after allogeneic stem cell transplantation // Annals of Hematology. 2019. Vol. 98, № 7.
Hevessy Z. et al. Algorithm of differential diagnosis of anemia involving laboratory medicine specialists to advance diagnostic excellence // Clin Chem Lab Med. 2024. Vol. 62, № 3.
Soma P., Ellemdin S., Mashoeshoe K.S. The differential diagnosis of HIV related anaemia should include pure red cell aplasia // HIV and AIDS Review. 2013. Vol. 12, № 4.
Teague D. et al. Hepatitis C Infection Associated with Acquired Pure Red Cell Aplasia // Trop Med Infect Dis. 2023. Vol. 8, № 1.
Fu R. et al. The clinical characteristics and therapy response of patients with acquired pure red cell aplasia // Hematology. 2018. Vol. 23, № 9.
Pivnik A. V. et al. Pure red cell aplasia with M-gradient: A literature review and clinical experience // Klinicheskaya Onkogematologiya/Clinical Oncohematology. 2018. Vol. 11, № 3.
Zhu P. et al. Prevalence of Pure Red Cell Aplasia Following Major ABO-Incompatible Hematopoietic Stem Cell Transplantation // Front Immunol. 2022. Vol. 13.
Shokrgozar N., Tamaddon G. ABO blood grouping mismatch in hematopoietic stem cell transplantation and clinical guides // International Journal of Hematology-Oncology and Stem Cell Research. 2018. Vol. 12, № 4.
Charles R.J. et al. The pathophysiology of pure red cell aplasia: Implications for therapy // Blood. 1996. Vol. 87, № 11.
Lacy M.Q., Kurtin P.J., Tefferi A. Pure red cell aplasia: Association with large granular lymphocyte leukemia and the prognostic value of cytogenetic abnormalities // Blood. 1996. Vol. 87, № 7.
Crabol Y. et al. Intravenous immunoglobulin therapy for pure red cell aplasia related to human parvovirus B19 infection: A retrospective study of 10 patients and review of the literature // Clinical Infectious Diseases. 2013. Vol. 56, № 7.
Thompson D.F., Gales M.A. Drug‐Induced Pure Red Cell Aplasia // Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy. 1996. Vol. 16, № 6.
Mouthon L., Guillevin L., Tellier Z. Intravenous immunoglobulins in autoimmune- or parvovirus B19-mediated pure red-cell aplasia // Autoimmunity Reviews. 2005. Vol. 4, № 5.
Kurhade K. et al. Multiple modalities in treating pediatric pure red cell aplasia: A case series // Pediatric Hematology Oncology Journal. 2023. Vol. 8, № 3.
Lobbes H. et al. Treatment strategy for acquired pure red cell aplasia: a systematic review and meta-analysis // Blood Advances. 2023. Vol. 7, № 21.
Biswal N., Narayanan P., Chetan G. Cyclosporine A responsive pure red cell aplasia in a child with systemic lupus erythematosus // Indian Journal of Hematology and Blood Transfusion. 2007. Vol. 23, № 3–4.
Long Z. et al. Successful treatment of refractory/relapsed acquired pure red cell aplasia with sirolimus // Ann Hematol. 2018. Vol. 97, № 11.
Huang Y. et al. Sirolimus is effective for refractory/relapsed/intolerant acquired pure red cell aplasia: results of a prospective single-institutional trial // Leukemia. 2022. Vol. 36, № 5.
Yang Y. et al. Sirolimus versus cyclosporine A in patients with primary acquired pure red cell aplasia: a prospective cohort study // Blood Cancer Journal. 2023. Vol. 13, № 1.
Salama Y. et al. Isolated anemia in patients with large granular lymphocytic leukemia (LGLL) // Blood Cancer J. 2022. Vol. 12, № 2.
Ghazal H. Successful treatment of pure red cell aplasia with rituximab in patients with chronic lymphocytic leukemia // Blood. 2002. Vol. 99, № 3.
Khan F. et al. Subcutaneous bortezomib is highly effective for pure red cell aplasia after ABO-incompatible haematopoietic stem cell transplantation // Transfusion Medicine. 2014. Vol. 24, № 3.
Harris S.I., Weinberg J.B. Treatment of red cell aplasia with antithymocyte globulin: Repeated inductions of complete remissions in two patients // Am J Hematol. 1985. Vol. 20, № 2.
Gomez-Arteaga A. et al. Use of anti-thymocyte globulin (ATG) for the treatment of pure red cell aplasia and immune-mediated cytopenias after allogeneic hematopoietic cell transplantation: a case series // Bone Marrow Transplantation. 2020. Vol. 55, № 12.
Mangla A H.H. Pure red cell aplasia // Treasure Island, FL: FL: StatPearls Publishing. 2021.
Passweg J.R., Rabusin M. Hematopoetic stem cell transplantation for immune thrombocytopenia and other refractory autoimmune cytopenias // Autoimmunity. 2008. Vol. 41, № 8.
Halkes C. et al. Allogeneic stem cell transplantation for acquired pure red cell aplasia // American Journal of Hematology. 2019. Vol. 94, № 11.
Кузьмина Л. А. Петинати Н. А. Л.Л.С. и др. Применение избирательной сорбции изогемагглютининов альфа у больной парциальной красноклеточной аплазией после трансплантации аллогенного костного мозга // Гематология и трансфузиология. 2011. P. 40–44.
Dellacasa C.M. et al. Efficacy of plasmapheresis for the treatment of pure red blood cell aplasia after allogeneic stem cell transplantation // Transfusion (Paris). 2015. Vol. 55, № 12.
Zhidong W., Hongmin Y., Hengxiang W. Successful treatment of pure red cell aplasia with a single low dose of rituximab in two patients after major ABO incompatible peripheral blood allogeneic stem cell transplantation // Transfusion Medicine. 2012. Vol. 22, № 4.
Busca A. et al. Eltrombopag for the Treatment of Refractory Pure RBC Aplasia after Major ABO Incompatible Hematopoietic Stem Cell Transplantation // Biology of Blood and Marrow Transplantation. 2018. Vol. 24, № 8.
Rautenberg C. et al. Daratumumab for treatment of pure red cell aplasia after allogeneic stem cell transplantation // Bone Marrow Transplantation. 2020. Vol. 55, № 6.
Martino R., García-Cadenas I., Esquirol A. Daratumumab may be the most effective treatment for post-engraftment pure red cell aplasia due to persistent anti-donor isohemagglutinins after major ABO-mismatched allogeneic transplantation // Bone Marrow Transplantation. 2022. Vol. 57, № 2.
Verholen F. et al. Resistant pure red cell aplasia after allogeneic stem cell transplantation with major ABO mismatch treated by escalating dose donor leukocyte infusion // Eur J Haematol. 2004. Vol. 73, № 6.
Marco-Ayala J. et al. Pure red cell aplasia after major or bidirectional ABO incompatible hematopoietic stem cell transplantation: to treat or not to treat, that is the question // Bone Marrow Transplantation. 2021. Vol. 56, № 4.
Thompson C.A., Steensma D.P. Pure red cell aplasia associated with thymoma: Clinical insights from a 50-year single-institution experience // Br J Haematol. 2006. Vol. 135, № 3.
Yen C.C. et al. Pure Red Cell Aplasia and Other Haematological Diseases Associated With Thymoma: A Case Series and Systematic Review // Front Med (Lausanne). 2021. Vol. 8.
Moriyama S. et al. Pure red cell aplasia associated with thymoma: A report of a single-center experience // J Thorac Dis. 2018. Vol. 10, № 8.
Камельских Д. В К.М.Е. Подбор компонентов донорской крови в случае трансплантации аллогенного костного мозга и/или аллогенных гемопоэтических стволовых клеток // Гематология и трансфузиология. 2022. P. 112–113.
Carreras E D.C.M.M.K.N. (editors). The EBMT Handbook: Hematopoietic Stem Cell Transplantation and Cellular Therapies, 7th edition. Cham (CH): Springer. 2019. 163–169 p.
Для продолжения работы требуется
Регистрация
Предыдущая страница
Следующая страница
Оглавление
Список сокращений
Термины и определения
Приобретенная чистая красноклеточная аплазия (эритробластопения)
+
Список литературы
Приложение А1. Состав рабочей группы по разработке и пересмотру клинических рекомендаций
Приложение А2. Методология разработки клинических рекомендаций
Приложение А3. Справочные материалы, включая соответствие показаний к применению и противопоказаний, способов применения и доз лекарственных препаратов, инструкции по применению лекарственного препарата
Приложение Б. Алгоритмы действий врача
Приложение В. Информация для пациента
Приложение Г1-ГN. Шкалы оценки, вопросники и другие оценочные инструменты состояния пациента, приведенные в клинических рекомендациях
Данный блок поддерживает скрол*