Journals / Turkish Journal of Hematology / 2010 / Cilt: 27 - Sayı: 4

Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi

Acquired pure megakaryocytic aplasia successfully treated with cyclosporine

Pages
289–293
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

Treatment with prednisone and intravenous immunoglobulin failed, but he was successfully treated with cyclosporine, with complete remission after 90 days and normal platelet count maintained thereafter.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow.
📊
Key Findings & Data:We report a case of a 25-year-old male diagnosed as acquired pure megakaryocytic aplasia.
💡
Conclusion & Impact:Treatment with prednisone and intravenous immunoglobulin failed, but he was successfully treated with cyclosporine, with complete remission after 90 days and normal platelet count maintained thereafter.
🔬Design:Research Article
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Abstract

Acquired pure megakaryocytic aplasia is a rare hematological disorder characterized by thrombocytopenia with absent or markedly reduced megakaryocytes in the bone marrow. We report a case of a 25-year-old male diagnosed as acquired pure megakaryocytic aplasia. Treatment with prednisone and intravenous immunoglobulin failed, but he was successfully treated with cyclosporine, with complete remission after 90 days and normal platelet count maintained thereafter.

Özet

Kazanılmış saf megakaryositik aplazi, kemik iliğinde namevcut ya da anlamlı ölçüde azaltılmış megakaryosit içeren trombositopeni ile karakterize, nadir hematolojik bir hastalıktır. Kazanılmış saf megakaryositik aplazi teşhisi konmuş, prednizon ve intravenöz immunoglobulin ile tedavisi başarısız olmuş ve siklosporin ile başarılı biçimde tedavi edilerek 90 gün sonra tam remisyona ulaşan ve ondan sonra platelet sayımı normalleşen 25 yaşında erkek bir olgunun raporu sunulmuştur.

🔖

Cite This Article

OMRI, H. E., İBRAHIM, F., TAHA, R. Y., NEGM, R. H., KHINJI, A. A., YASSIN, M., HAJJI, İ. A., AYOUBI, H. E., BADEN, H. (2010). Siklosporin ile başarılı şekilde tedavi edilen kazanılmış saf megakaryositik aplazi. Turkish Journal of Hematology, Cilt: 27 - Sayı: 4, 289–293. https://ajindex.com/articles/412955

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (12)

  1. Felderbauer P, Ritter PR, Mattern D, Schmitz F, Bulut K, Ansorge N, Schmitt-Graeff A, Schmidt WE, Baier JE. Acquired pure megakaryocytic aplasia: a separate haematological disease entity or a syndrome with multiple causes? Eur J Haematol 2004;72:451-4
  2. Bhattacharyya J, Kumar R, Tyagi S, Kishore J, Mahapatra M, Choudhry VP. Human parvovirus B19-induced acquired pure amegakaryocytic thrombocytopenia. Br J Haematol 2005;128:128-9
  3. Kuwana M, Kaburaki J, Okazaki Y, Miyazaki H, Ikeda Y. Two types of autoantibody-mediated thrombocytopenia in patients with systemic lupus erythematosus. Rheumatology (Oxford) 2006;45:851-4
  4. Katsumata Y, Suzuki T, Kuwana M, Hattori Y, Akizuki S, Sugiura H, Matsuoka Y. Anti-c-Mpl (thrombopoietin receptor) autoantibody-induced amegakaryocytic thrombocytopenia in a patient with systemic sclerosis. Arthritis Rheum 2003;48:1647-51
  5. Chaudhary UB, Eberwine SF, Hege KM. Acquired amegakaryocytic thrombocytopenia purpura and eosinophilic fasciitis: a long relapsing and remitting course. Am J Hematol 2004;75:146-50
  6. Maslovsky I, Gefel D, Uriev L, Ben Dor D, Lugassy G. Malignant thymoma complicated by amegakaryocytic thrombocytopenic purpura. Eur J Intern Med 2005;16:523-4
  7. Lai DW, Loughran TP Jr, Maciejewski JP, Sasu S, Song SX, Epling-Burnette PK, Paquette RL. Acquired amegakaryocytic thrombocytopenia and pure red cell aplasia associated with occult large granular lymphocyte leukemia. Leuk Res 2008;32:823-7
  8. King JA, Elkhalifa MY, Latour LF. Rapid progression of acquired amegakaryocytic thrombocytopenia to aplastic anemia. Southern Med J 1997;90:91-4
  9. Erkurt MA, Kaya E, Baran M, Yitmen E, Snel S, Kuku I, Aydogdu I. Rapid progression of acquired amegakaryocytic thrombocytopenia to myelodysplastic syndrome: case report. Turk J Haematol 2005;22:205-8
  10. Niparuck P, Atichatakarn V, Chuncharunee S. Successful treatment of acquired amegakaryocytic thrombocytopenic purpura refractory to corticosteroids and intravenous immunoglobulin with antithymocyte globulin and cyclosporin. Int J Hematol 2008;88:223-6
  11. Benedetti F, de Sabata D, Perona G. T suppressor activated lymphocytes (CD8+/DR+) inhibit megakaryocyte progenitor cell differentiation in a case of acquired amegakaryocytic thrombocytopenic purpura. Stem Cells 1994;12):205-13
  12. Katai M, Aizawa T, Ohara N, Hiramatsu K, Hashizume K, Yamada T, Kitano K, Saito H, Shinoda T, Wakata S, Nakahata T. Acquired amegakaryocytic thrombocytopenic purpura with humoral inhibitor