نتایج جستجو برای: myelodysplastic syndrome

تعداد نتایج: 625034  

Journal: :Haematologica 2016
Michaela Nováková Markéta Žaliová Martina Suková Marcin Wlodarski Aleš Janda Eva Froňková Vít Campr Kateřina Lejhancová Ondřej Zapletal Dagmar Pospíšilová Zdeňka Černá Tomáš Kuhn Peter Švec Vendula Pelková Zuzana Zemanová Gitte Kerndrup Marry van den Heuvel-Eibrink Vincent van der Velden Charlotte Niemeyer Tomáš Kalina Jan Trka Jan Starý Ondřej Hrušák Ester Mejstříková

GATA-2 deficiency was recently described as common cause of overlapping syndromes of immunodeficiency, lymphedema, familiar myelodysplastic syndrome or acute myeloid leukemia. The aim of our study was to analyze bone marrow and peripheral blood samples of children with myelodysplastic syndrome or aplastic anemia to define prevalence of the GATA2 mutation and to assess whether mutations in GATA-...

2014
Fernando Barroso Duarte Romelia Pinheiro Gonçalves Maritza Cavalcante Barbosa Francisco Dário Rocha Filho Talyta Ellen de Jesus dos Santos Thayna Nogueira dos Santos Paulo Roberto Leitão de Vasconcelos

BACKGROUND At the time of diagnosis, more than 50% of patients with myelodysplastic syndrome have a normal karyotype and are classified as having a favorable prognosis. However, these patients often show very variable clinical outcomes. Furthermore, current diagnostic tools lack the ability to look at genetic factors beyond karyotyping in order to determine the cause of this variability. OBJE...

Journal: :Haematologica 2002
Fernando Ramos Marta Fuertes-Núñez Dimas Suárez-Vilela Arsenio Fernández-López

BACKGROUND AND OBJECTIVES Apoptosis is thought to play a key pathogenic role in myelodysplastic syndrome. The aim of our study was to determine whether apoptotic index, p53 and bcl-2 levels correlate with the clinical consequences of ineffective hematopoiesis; namely, the development of cytopenia and the shortened survival of patients with myelodysplastic syndrome. DESIGN AND METHODS The apop...

Journal: :Singapore medical journal 2007
J Abdul-Wahab M Naznin A Suhaimi A R Amir-Hamzah

Familial myelodysplastic syndrome occurring at a young age is a very rare childhood haematological malignancy. Two siblings, aged three and 18 years, from a consanguineous marriage, presented with pancytopenia and was subsequently diagnosed to have myelodysplastic syndrome. Both remained clinically stable throughout the illness. Splenectomy appeared to have fully corrected the cytopenia in one ...

Journal: :Haematologica 2008
Stephanie Struski Laurent Mauvieux Carine Gervais Catherine Hélias Kun Lun Liu Michel Lessard

The ETV6/GOT1 fusion, resulting from t(10;12) (q24;p13), has been recently described in a myelodysplastic syndrome. We reported a second case of t(10;12)-positive myelodysplastic syndrome in whom fluorescent in situ hybridization confirmed the non-random translocation but molecular biology analyses revealed a ETV6/GOT1 chimera varying from the first case described.

Journal: :Haematologica 2014
Heesun J Rogers James W Vardiman John Anastasi Gordana Raca Natasha M Savage Athena M Cherry Daniel Arber Erika Moore Jennifer J D Morrissette Adam Bagg Yen-Chun Liu Susan Mathew Attilio Orazi Pei Lin Sa A Wang Carlos E Bueso-Ramos Kathryn Foucar Robert P Hasserjian Ramon V Tiu Matthew Karafa Eric D Hsi

Acute myeloid leukemia and myelodysplastic syndrome with inv(3)(q21q26.2)/t(3;3)(q21;q26.2) have a poor prognosis. Indeed, the inv(3)(q21q26.2)/t(3;3)(q21;q26.2) has been recognized as a poor risk karyotype in the revised International Prognostic Scoring System. However, inv(3)(q21q26.2)/t(3;3)(q21;q26.2) is not among the cytogenetic abnormalities pathognomonic for diagnosis of acute myeloid le...

2008
P. Chu R. Aitchison

Cutaneous manifestations of haematological malignancies, although well recognized in acute monoblastic leukaemia and lymphoma, are relatively uncommon in primary myelodysplastic syndrome (MDS), which is a group of heterogeneous disorders formerly known as pre-leukaemia. Previously reported cases of skin involvement in this syndrome have been confined to a sub-type of MDS, namely chronic myelomo...

2014
Hiroto Kaneko Kazuho Shimura Saeko Kuwahara Muneo Ohshiro Yasuhiko Tsutsumi Toshiki Iwai Shigeo Horiike Shouhei Yokota Yasuo Ohkawara Masafumi Taniwaki

INTRODUCTION Deletions of chromosome 7 are often detected in myelodysplastic syndrome. The most commonly deleted segments are clustered at band 7q22. A critical gene is therefore suggested to be located in this region. We report a patient with myelodysplastic syndrome whose marrow cells carried an inversion of 7q22 and q36 as a sole karyotypic abnormality. How this extremely rare chromosomal ab...

Journal: :Archives of pathology & laboratory medicine 2005
Deven Scurlock Daniel Ostler Andy Nguyen Amer Wahed

Ellis-van Creveld (EVC) syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder characterized by a variable spectrum of clinical findings. Classical EVC syndrome comprises a tetrad of clinical manifestations of chondrodystrophy, polydactyly, ectodermal dysplasia, and cardiac defects. In several case reports, dysplasia involving other organs has also been identified. Hemat...

Journal: :International journal of molecular sciences 2016
Eugenia Flores-Figueroa Dita Gratzinger

We review the murine and human microenvironment and hematopoietic stem cell niche in the context of intact bone marrow architecture in man and mouse, both in normal and in myelodysplastic syndrome marrow. We propose that the complexity of the hematopoietic stem cell niche can usefully be approached in the context of its topobiology, and we provide a model that incorporates in vitro and in vivo ...

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