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  1. Article ; Online: Atypical amyloid deposits.

    Jorge, Iago Farias / Kaufman, Jacques / Hirth, Carlos Gustavo

    International journal of hematology

    2016  Volume 104, Issue 4, Page(s) 409–410

    MeSH term(s) Amyloidosis/pathology ; Animals ; Humans ; Plaque, Amyloid/pathology
    Language English
    Publishing date 2016-10
    Publishing country Japan
    Document type Letter
    ZDB-ID 1076875-0
    ISSN 1865-3774 ; 0917-1258 ; 0925-5710
    ISSN (online) 1865-3774
    ISSN 0917-1258 ; 0925-5710
    DOI 10.1007/s12185-016-2066-3
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    In stock of ZB MED Cologne/Königswinter

    Zs.A 269: Show issues Location:
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  2. Article ; Online: Sézary syndrome with T/NK phenotype: A variant phenotype or a distinct clinical entity?

    Matos, Daniel Mazza / Kaufman, Jacques / Scrideli, Carlos Alberto / Falcão, Roberto Passetto

    Cytometry. Part B, Clinical cytometry

    2016  Volume 94, Issue 4, Page(s) 561–563

    MeSH term(s) Humans ; Lymphoma, Extranodal NK-T-Cell/immunology ; Lymphoma, Extranodal NK-T-Cell/pathology ; Male ; Middle Aged ; Phenotype ; Sezary Syndrome/immunology ; Sezary Syndrome/pathology ; Skin Neoplasms/immunology ; Skin Neoplasms/pathology
    Language English
    Publishing date 2016-10-28
    Publishing country United States
    Document type Case Reports ; Letter
    ZDB-ID 2099657-3
    ISSN 1552-4957 ; 1552-4949 ; 0196-4763
    ISSN (online) 1552-4957
    ISSN 1552-4949 ; 0196-4763
    DOI 10.1002/cyto.b.21381
    Database MEDical Literature Analysis and Retrieval System OnLINE

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    In stock of ZB MED Cologne/Königswinter

    Zs.A 1688: Show issues Location:
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  3. Article ; Online: Abnormal ABO typing.

    Brunetta, Denise M / Kaufman, Jacques / Albuquerque, Lilian M de / Carlos, Luciana M de Barros / Barroso-Duarte, Fernando

    British journal of haematology

    2015  Volume 171, Issue 1, Page(s) 12

    MeSH term(s) ABO Blood-Group System/blood ; Adult ; Blood Grouping and Crossmatching ; Female ; Hematologic Neoplasms/blood ; Humans
    Chemical Substances ABO Blood-Group System
    Language English
    Publishing date 2015-10
    Publishing country England
    Document type Case Reports ; Journal Article
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.13565
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  4. Article: T-cell/myeloid mixed-phenotype acute leukemia with monocytic differentiation and isolated 17p deletion.

    Lopes, Germison Silva / Leitão, João Paulo de Vasconcelos / Kaufman, Jacques / Duarte, Fernando Barroso / Matos, Daniel Mazza

    Revista brasileira de hematologia e hemoterapia

    2014  Volume 36, Issue 4, Page(s) 293–296

    Abstract: Mixed phenotype acute leukemia is a rare subtype of leukemia that probably arises from a hematopoietic pluripotent stem cell. The co-expression of two of myeloid, B- or T-lymphoid antigens is the hallmark of this disease. Herein, the case of a 28-year- ... ...

    Abstract Mixed phenotype acute leukemia is a rare subtype of leukemia that probably arises from a hematopoietic pluripotent stem cell. The co-expression of two of myeloid, B- or T-lymphoid antigens is the hallmark of this disease. Herein, the case of a 28-year-old female patient is reported who presented with hemoglobin of 5.8g/dL, white blood cell count of 138×10(9)/L and platelet count of 12×10(9)/L. The differential count of peripheral blood revealed 96% of blasts. Moreover, the patient presented with lymphadenopathy, splenomegaly and bone marrow infiltration by monocytoid blasts characterized as 7% positivity by Sudan Black cytochemical staining. Immunophenotyping revealed the involvement of blasts of both T- and monocytic lineages. The cytogenetic analysis showed an isolated 17p deletion. Thus, the diagnosis of T-cell/myeloid mixed phenotype acute leukemia was made with two particular rare features, that is, the monocytic differentiation and the 17p deletion as unique cytogenetic abnormalities. The possibility of concomitant expressions of T-cell and monocytic differentiation antigens in the same blast population is hard to explain using the classical model of hematopoiesis. However, recent studies have suggested that myeloid potential persists even when the lineage branches segregate toward B- and T-cells. The role of an isolated 17p deletion in the pathogenesis of this condition is unclear. At present, the patient is in complete remission after an allogeneic stem cell transplantation procedure.
    Language English
    Publishing date 2014-04-03
    Publishing country Brazil
    Document type Journal Article
    ZDB-ID 2105177-X
    ISSN 1806-0870 ; 1516-8484
    ISSN (online) 1806-0870
    ISSN 1516-8484
    DOI 10.1016/j.bjhh.2014.03.004
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  5. Article ; Online: Oro-nasal myiasis in a lymphoma patient.

    Jorge, Iago F / de Santana, Luiz R P / Silveira, Marcos A A / Brunetta, Denise M / Kaufman, Jacques / Barroso-Duarte, Fernando

    British journal of haematology

    2016  Volume 175, Issue 5, Page(s) 757

    Language English
    Publishing date 2016-12
    Publishing country England
    Document type Journal Article
    ZDB-ID 80077-6
    ISSN 1365-2141 ; 0007-1048
    ISSN (online) 1365-2141
    ISSN 0007-1048
    DOI 10.1111/bjh.14319
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  6. Article ; Online: Wernicke's encephalopathy in a patient with non-Hodgkin's lymphoma post-Autologous HSCT.

    Leitão, João Paulo de Vasconcelos / Lemes, Romélia Pinheiro Gonçalves / Barbosa, Maritza Cavalcante / Araújo, Beatriz Stela Gomes de Souza Pitombeira / Barroso, Karine Sampaio Nunes / Kaufman, Jacques / Santos, Talyta Ellen de Jesus Dos / Moura, Anna Thawanny Gadelha / Barreto, André Rodrigues Façanha / Duarte, Fernando Barroso

    Revista da Associacao Medica Brasileira (1992)

    2018  Volume 64, Issue 10, Page(s) 882–884

    Abstract: Wernick's Encephalopathy (WE) is an acute neuropsychiatric syndrome caused by thiamine deficiency post hematopoietic stem cell transplant (HSCT). WE is associated with high mortality and morbidity rates, but due to its rare occurrence, it is rarely ... ...

    Abstract Wernick's Encephalopathy (WE) is an acute neuropsychiatric syndrome caused by thiamine deficiency post hematopoietic stem cell transplant (HSCT). WE is associated with high mortality and morbidity rates, but due to its rare occurrence, it is rarely considered in patients submitted to this procedure. Considering that, the manuscript reports the clinical characteristics and the possible factors that predisposed the occurrence of WE in a patient with non-Hodgkin's lymphoma post-Autologous HSCT. We conclude that WE should be considered in patients submitted to autologous HSCT associated with prolonged use of TPN and malnutrition.
    MeSH term(s) Adult ; Female ; Hematopoietic Stem Cell Transplantation/adverse effects ; Humans ; Lymphoma, Non-Hodgkin/therapy ; Risk Factors ; Thiamine Deficiency/complications ; Transplantation, Autologous ; Wernicke Encephalopathy/diagnostic imaging ; Wernicke Encephalopathy/etiology
    Language English
    Publishing date 2018-12-03
    Publishing country Brazil
    Document type Case Reports ; Journal Article
    ZDB-ID 2027973-5
    ISSN 1806-9282 ; 0104-4230
    ISSN (online) 1806-9282
    ISSN 0104-4230
    DOI 10.1590/1806-9282.64.10.882
    Database MEDical Literature Analysis and Retrieval System OnLINE

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  7. Article ; Online: Successful hematopoietic stem cell mobilization with vinorelbine and filgrastim in germ cell tumor.

    Carneiro-Silva, Fabiana Aguiar / Brunetta, Denise Menezes / Kaufman, Jacques / Leitão, João Paulo Vasconcelos / Barroso, Karine Sampaio Nunes / Barbosa, Suzanna Araújo Tavares / Carlos, Luciana Maria de Barros / Barroso-Duarte, Fernando

    Clinical and experimental medicine

    2017  Volume 17, Issue 3, Page(s) 417–418

    Abstract: Germ cell tumor (GCT) is the most frequent cancer in young men and is highly curable. Almost 80 % of patients with the disease in an advanced stage achieve a reliable response to cisplatin combination chemotherapy. For relapsing or refractory disease, ... ...

    Abstract Germ cell tumor (GCT) is the most frequent cancer in young men and is highly curable. Almost 80 % of patients with the disease in an advanced stage achieve a reliable response to cisplatin combination chemotherapy. For relapsing or refractory disease, autologous hematopoietic stem cell transplantation (HSCT) is an effective therapy. The two most used mobilization strategies for HSC collection are filgrastim alone or filgrastim after chemotherapy (chemomobilization). HSC collection with filgrastim mobilization can be difficult, especially in highly treated patients. While the addition of chemotherapy improves mobilization and reduces the number of apheresis sessions, it can increase morbidity rate as well. We describe a case of a 45-year-old male with classical seminoma who was submitted to orchiectomy. Two months after, he presented progression of the tumor. He received four cycles of cisplatin, etoposide and bleomycin, with residual retroperitoneal mass and cervical lymphadenopathy. Further, he was submitted to three more cycles of cisplatin, ifosfamide and paclitaxel. Thereupon, he showed partial response. At that moment, autologous HSC transplantation was considered. In the first mobilization, filgrastim alone was used without success in harvesting. The second mobilization consisted of vinorelbine at day 1 (35 mg/m
    Language English
    Publishing date 2017-08
    Publishing country Italy
    Document type Letter
    ZDB-ID 2053018-3
    ISSN 1591-9528 ; 1591-8890
    ISSN (online) 1591-9528
    ISSN 1591-8890
    DOI 10.1007/s10238-016-0425-2
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    In stock of ZB MED Cologne/Königswinter

    Zs.A 5481: Show issues Location:
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  8. Article ; Online: Relevance of prognostic factors in the decision-making of stem cell transplantation in Myelodysplastic Syndromes.

    Duarte, Fernando Barroso / Santos, Talyta Ellen de Jesus Dos / Barbosa, Maritza Cavalcante / Kaufman, Jacques / Vasconcelos, João Paulo de / Lemes, Romélia Pinheiro Gonçalves / Rocha, Francisco Dário / Coutinho, Diego Ferreira / Zalcberg, Ilana / Vasconcelos, Paulo Roberto Leitão de

    Revista da Associacao Medica Brasileira (1992)

    2016  Volume 62 Suppl 1, Page(s) 25–28

    Abstract: The hematopoietic stem cell transplantation (HSCT) is the only curative alternative for Myelodysplastic Syndrome (MDS), but many patients are not eligible for this treatment, as there are several limiting factors, especially in the case of patients with ... ...

    Abstract The hematopoietic stem cell transplantation (HSCT) is the only curative alternative for Myelodysplastic Syndrome (MDS), but many patients are not eligible for this treatment, as there are several limiting factors, especially in the case of patients with low-risk MDS. The aim of this study is to discuss the factors that can guide the decision-making on referring or not a patient to HSCT. Three cases of MDS, two of which were submitted to HSCT are presented. We intend to report the difficulties in referring patients with MDS to transplant and the prognostic factors that contribute to define eligibility.
    MeSH term(s) Aged ; Decision Making ; Fatal Outcome ; Hematopoietic Stem Cell Transplantation/methods ; Humans ; Male ; Middle Aged ; Myelodysplastic Syndromes/pathology ; Myelodysplastic Syndromes/surgery ; Prognosis ; Risk Assessment
    Language English
    Publishing date 2016-10
    Publishing country Brazil
    Document type Case Reports ; Journal Article
    ZDB-ID 2027973-5
    ISSN 1806-9282 ; 0104-4230
    ISSN (online) 1806-9282
    ISSN 0104-4230
    DOI 10.1590/1806-9282.62.suppl1.25
    Database MEDical Literature Analysis and Retrieval System OnLINE

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