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Hemophagocytic Lymphohistiocytosis Secondary to Juvenile Myelomonocytic Leukemia: A Case Report and Review of the Literature

Autor: Leping Zhang, Jiong Qin, Fang-Yuan Zheng, Yueping Jia

Publikováno v: Journal of pediatric hematology/oncology. 44(2)

RATIONALE Juvenile myelomonocytic leukemia (JMML) is a rare hematopoietic disorder, which is more rarely accompanied by monosomy 5 or deletion of the long arm of chromosome 5q (-5/5q-) or monosomy 5 (5q-/-5), and hemophagocytic lymphohistiocytosis (H

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5d24272c257b94d0aa83adcdfaa536c8
https://pubmed.ncbi.nlm.nih.gov/34862352

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Spectrum of myelodysplastic syndrome in patients evaluated for cytopenia(s). A Report from a Reference Centre in Saudi Arabia

Autor: Ayman Mashi, Tarek Owaidah, Suleimman A. Al-Sweedan, Shahrukh K. Hashmi, Haitham Khogeer, Nour AlMozain, Thomas Morris, Nasir Bakshi, Randa Alnounou, Amal T Al-Omran, Salem Khalil, Qasem Alneami

Publikováno v: Hematology/Oncology and Stem Cell Therapy.

Background/Objective Myelodysplastic syndrome (MDS) is a clonal disorder of hematopoietic stem cells, characterized by ineffective hematopoiesis, peripheral cytopenias along with hypercellularity of the bone marrow, and marked dysplastic features. Es

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::005662da6a96c3e277eefe5d0cda9d6a
https://doi.org/10.1016/j.hemonc.2020.11.001

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Acute leukaemia with a pure erythroid phenotype: under-recognized morphological and cytogenetic signatures associated universally with primary refractory disease and a dismal clinical outcome

Autor: Neval Ozkaya, David C. Park, Scott B. Lovitch

Publikováno v: Histopathology. 71:316-321

Aims Pure erythroid leukemia (PEL) is a very rare and aggressive subtype of acute myeloid leukemia defined by the World Health Organization (WHO) as a neoplastic proliferation of immature cells committed exclusively to the erythroid lineage comprisin

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https://doi.org/10.1111/his.13207

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Allogeneic stem cell transplantation using HLA-matched donors for acute myeloid leukemia with deletion 5q or monosomy 5 : a study from the Acute Leukemia Working Party of the EBMT

Autor: Arnold Ganser, Jan J. Cornelissen, Xavier Poiré, Ibrahim Yakoub-Agha, Mauricette Michallet, Liisa Volin, Didier Blaise, Edouard Forcade, Jürgen Finke, Jordi Esteve, Mohamad Mohty, Arnon Nagler, Myriam Labopin, Carlos Richard Espiga, Johan Maertens, Emmanuelle Polge

Publikováno v: Haematologica, 105(2), 414-423. Ferrata Storti Foundation
Haematologica

Deletion 5q or monosomy 5 (-5/5q-) in acute myeloid leukemia (AML) is a common high-risk feature that is referred to allogeneic stem cell transplantation. However, -5/5q- is frequently associated with other high-risk cytogenetic aberrations such as c

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4166a9643fd3709a85aac3ae0f07b1b0
http://hdl.handle.net/10138/313286

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Validation of Fluorescence In Situ Hybridization (FISH) for Chromosome 5 Monosomy and Deletion

Autor: Susan M. Zneimer

Publikováno v: Current protocols in human geneticsLiterature Cited. 105(1)

In order to comply with regulations set by established local, state, and federal agencies and other regulatory organizations, such as the College of American Pathologists and the International Organization for Standardization, a clinical laboratory n

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https://pubmed.ncbi.nlm.nih.gov/31922364

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The impact of concomitant cytogenetic abnormalities on acute myeloid leukemia with monosomy 7 or deletion 7q after HLA-matched allogeneic stem cell transplantation

Publikováno v: American Journal of Hematology, 95(3), 282-294. Wiley-Liss Inc.

Monosomy 7 or deletion 7q (-7/7q-) is the most frequent adverse cytogenetic features reported in acute myeloid leukemia (AML), and is a common indication for allogeneic stem cell transplantation (SCT). Nevertheless, -7/7q- occurs frequently with othe

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https://pubmed.ncbi.nlm.nih.gov/31876307

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TP53 mutations are associated with very complex karyotype and suggest poor prognosis in newly diagnosed myelodysplastic syndrome patients with monosomal karyotype

Autor: Yanling Ren, Shuanghong Zhu, Jie Jin, Hua Zhang, Lingxu Jiang, Yingwan Luo, Hongyan Tong, Li Ye, Xinping Zhou, Jinghan Wang, Chen Mei, Lu Wang

Publikováno v: Asia-Pacific journal of clinical oncologyREFERENCES. 16(3)

AIM The aim of this study was to evaluate the clinical and molecular characteristics of myelodysplastic syndrome (MDS) patients with monosomal karyotype (MK). METHODS Eighty MDS patients with MK diagnosed between January 2010 and December 2018 were i

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https://pubmed.ncbi.nlm.nih.gov/32030889

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A new complex karyotype in a unique de novo myelodysplastic syndrome case involving ten chromosomes and monoallelic loss of TP53

Autor: Abdulmunim Aljapawe, Thomas Liehr, Walid Al-Achkar, Manar As’sad, Abdulsamad Wafa

Publikováno v: Gene Reports. 4:208-212

Myelodysplastic syndrome (MDS) is a group of clonal stem cell disorders characterized by cytopenia, dysplasia in one or more cell lineages, and ineffective hematopoiesis. MDS is associated with high risk of progression to acute myeloid leukemia. At i

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::955322bbb81bff044c0feafbfacb71aa
https://doi.org/10.1016/j.genrep.2016.05.005

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Gingival Ulcerations in a Patient with Acute Myeloid Leukemia: A Case Report and Literature Review

Autor: Mirta Mikulić, Danica Vidović Juras, Vanja Vučićević Boras, Sandra Bašić-Kinda, Igor Aurer

Publikováno v: Acta clinica Croatica
Volume 58.
Issue 3.
Acta Clinica Croatica

A 40-year-old female patient was admitted to the Department of Oral Medicine due to oral ulcerations. Oral ulcerations were present on vestibular mucosa above teeth 21, 22, 25 and 26 and were 1 cm in diam-eter, and also around teeth 45 and 46. The pa

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https://hrcak.srce.hr/file/334793

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Cytogenetic Profiles of 472 Indian Children with Acute Myeloid Leukemia

Autor: Raja Pramanik, Sameer Bakhshi, Anudishi Tyagi, Shilpi Chaudhary, Anita Chopra

Publikováno v: Indian pediatrics. 55(6)

OBJECTIVE To analyze the cytogenetic abnormalities of a large cohort of consecutive pediatric Acute Myeloid Leukemia (AML) patients, treated on a uniform protocol. DESIGN Review of case records. SETTING Pediatric Cancer Center of tertiary care hospit

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https://pubmed.ncbi.nlm.nih.gov/30587658

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