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  1. AU="Lin, Li-Er"
  2. AU=Goulard Marie
  3. AU=Rosner Mitchell H
  4. AU="Murphy, Bríd"
  5. AU="Tsuneyoshi, Isao"
  6. AU="Tram, Le Thi Hong"
  7. AU="Veli-Pekka Jaakola"
  8. AU="Erduğan, Hüseyin"

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  1. Artikel ; Online: A rare BCR-ABL1 transcript in chronic myeloid leukemia: Case report and literature review.

    Zhao, Zhen-Yu / Tang, Nan / Lin, Li-Er

    Leukemia research

    2023  Band 133, Seite(n) 107369

    Abstract: Background: The purpose of this report is to enhance our scientific understanding of the clinicopathologic features of chronic myeloid leukemia (CML) with the e12a3 transcript and to provide insights into potential treatment options for this rare ... ...

    Abstract Background: The purpose of this report is to enhance our scientific understanding of the clinicopathologic features of chronic myeloid leukemia (CML) with the e12a3 transcript and to provide insights into potential treatment options for this rare subtype of CML.
    Case summary: We present the case of a 21-year-old Chinese male patient who was diagnosed with chronic myeloid leukemia (CML) with the e12a3 transcript. Biopsy of his left iliac soft tissue mass indicated that he was in the blast crisis phase of CML. The patient was treated with tyrosine kinase inhibitor (TKI) drugs and achieved remission, but relapsed soon after. Despite receiving prognostic chemotherapy, the disease progressed and eventually led to the patient's death.
    Conclusion: To avoid missed diagnosis and misdiagnosis, it is recommended to conduct a thorough clinical evaluation and actively identify the underlying etiology.
    Mesh-Begriff(e) Male ; Humans ; Young Adult ; Adult ; Fusion Proteins, bcr-abl/genetics ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/diagnosis ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/drug therapy ; Leukemia, Myelogenous, Chronic, BCR-ABL Positive/genetics ; Blast Crisis/genetics ; Blast Crisis/drug therapy ; Prognosis ; Protein Kinase Inhibitors
    Chemische Substanzen Fusion Proteins, bcr-abl (EC 2.7.10.2) ; Protein Kinase Inhibitors
    Sprache Englisch
    Erscheinungsdatum 2023-08-08
    Erscheinungsland England
    Dokumenttyp Case Reports ; Review ; Letter ; Research Support, Non-U.S. Gov't
    ZDB-ID 752396-8
    ISSN 1873-5835 ; 0145-2126
    ISSN (online) 1873-5835
    ISSN 0145-2126
    DOI 10.1016/j.leukres.2023.107369
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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  2. Artikel: Secondary light chain amyloidosis with Waldenström's macroglobulinemia and intermodal marginal zone lymphoma: A case report.

    Zhao, Zhen-Yu / Tang, Nan / Fu, Xiang-Jun / Lin, Li-Er

    World journal of clinical cases

    2019  Band 10, Heft 29, Seite(n) 10779–10786

    Abstract: Background: The co-existence of Waldenström's macroglobulinemia (WM) with internodal marginal zone lymphoma (INMZL) is rare and often associated with poor prognosis.: Case summary: We present a Chinese female patient who developed secondary light ... ...

    Abstract Background: The co-existence of Waldenström's macroglobulinemia (WM) with internodal marginal zone lymphoma (INMZL) is rare and often associated with poor prognosis.
    Case summary: We present a Chinese female patient who developed secondary light chain amyloidosis due to WM and INMZL and provides opinions on its systemic treatment. A 65-year-old woman was diagnosed with WM 6 years ago and received Bruton tyrosine kinase inhibitor monotherapy for two years. Her INMZL was confirmed due to left cervical lymphadenopathy. The patient presented with oedema in both lower limbs one year ago, and was diagnosed with secondary light chain amyloidosis. Treatment with the BC regimen (rituximab 375 mg/m
    Conclusion: A detailed clinical evaluation and active identification of the aetiology are recommended to avoid missed diagnosis and misdiagnosis.
    Sprache Englisch
    Erscheinungsdatum 2019-11-13
    Erscheinungsland United States
    Dokumenttyp Case Reports
    ISSN 2307-8960
    ISSN 2307-8960
    DOI 10.12998/wjcc.v10.i29.10779
    Datenquelle MEDical Literature Analysis and Retrieval System OnLINE

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