Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well‐controlled HIV patient: Case report and literature review

Myelodysplastic syndrome with clonal karyotype evolution associated with trisomy 8 and ASXL1 mutation in well‐controlled HIV patient: Case report and literature review

Bibliographic Details
Main Authors:	Daniela Palheiro Mendes‐de‐Almeida, Viviane Lamim Lovatel, Filipe Vicente dosSantos‐Bueno, Elaiza Almeida Antônio deKós, Francianne Gomes Andrade, Marcia Trindade Schramm, Estevão Portela Nunes, Beatriz Gilda J. Grinsztejn, Maria S Pombo‐de‐Oliveira, Teresa de Souza Fernandez
Format:	Article
Language:	English
Published:	Wiley 2020-07-01
Series:	eJHaem
Online Access:	https://doi.org/10.1002/jha2.14

Similar Items

Clinical and Prognostic Features in a Young Adult Patient with de novo Myelodysplastic Syndrome presenting t(11;16) (q23; q24)
by: Viviane Lamim Lovatel, et al.
Published: (2022-01-01)

When karyotype is decisive for myelodysplastic syndromes diagnosis
by: Aline dos Santos Borgo Perazzio, et al.
Published: (2019-10-01)

Trisomy X and myelodysplastic syndrome (MDS) with eosinophilia
by: Mohd Tohit, Eusni Rahayu, et al.
Published: (2012)

PB1997: TRISOMY 18 IN MYELODYSPLASTIC SYNDROMES
by: Nouha Bouayed Abdelmoula, et al.
Published: (2023-08-01)

A Novel Constitutional t(3;8)(p26;q21) and <i>ANKRD26</i> and <i>SRP72</i> Variants in a Child with Myelodysplastic Neoplasm: Clinical Implications
by: Viviane Lamim Lovatel, et al.
Published: (2023-04-01)

Frequent mutation of the polycomb-associated gene ASXL1 in the myelodysplastic syndromes and in acute myeloid leukemia.
by: Boultwood, J, et al.
Published: (2010)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 in the Myelodysplastic Syndromes and in Acute Myeloid Leukaemia
by: Boultwood, J, et al.
Published: (2009)

ASXL2 mutated myelodysplastic syndrome in a novel germline G6b variant
by: Shiqiang Qu, et al.
Published: (2022-01-01)

Genomic variations in patients with myelodysplastic syndrome and karyotypes without numerical or structural changes
by: Cristiano Luiz Ribeiro, et al.
Published: (2021-02-01)

Trisomy 8, a Cytogenetic Abnormality in Myelodysplastic Syndromes, Is Constitutional or Not?
by: Sílvia Saumell, et al.
Published: (2015-01-01)

Analysis of core mutation and TET2/ASXL1 mutations DNA methylation profile in myelodysplastic syndrome
by: Yue Feng, et al.
Published: (2023-12-01)

ASXL1 mutation as a surrogate marker in acute myeloid leukemia with myelodysplasia‐related changes and normal karyotype
by: Concepción Prats‐Martín, et al.
Published: (2020-06-01)

Prognosis and risk factors for ASXL1 mutations in patients with newly diagnosed acute myeloid leukemia and myelodysplastic syndrome
by: Liqing Yang, et al.
Published: (2024-01-01)

Molecular characterisation of ASXL1-mutant clonal haematopoiesis
by: Groom, AJ
Published: (2024)

The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome
by: Satoko Oka, et al.
Published: (2020-01-01)

Complex karyotype in myelodysplastic syndromes: Diagnostic procedure and prognostic susceptibility
by: Mohammad Shahjahani, et al.
Published: (2019-02-01)

Expression Profiles of DNA Methylation and Demethylation Machinery Components in Pediatric Myelodysplastic Syndrome: Clinical Implications
by: Lamim Lovatel V, et al.
Published: (2020-01-01)

Frequent Mutation of the Polycomb-Associated Gene ASXL1 In Acute Myeloid Leukemia Secondary to Myelodysplastic Syndrome or Chronic Myelomonocytic Leukemia
by: Fernandez-Mercado, M, et al.
Published: (2010)

COMPARATIVE STUDIES OF THE CHROMOSOMAL ARRANGEMENT IN THE C-METAPHASE BETWEEN NORMAL KARYOTYPE AND TRISOMY-21
by: E. Korn; G. Schwanitz, et al.
Published: (1987-06-01)

ASSOCIATION BETWEEN LEUKEMIC EVOLUTION AND UNCOMMON CHROMOSOMAL ALTERATIONS IN PEDIATRIC MYELODYSPLASTIC SYNDROME
by: Viviane Lamim Lovatel, et al.
Published: (2024-01-01)

Examining the neurodevelopmental and motor phenotypes of Bohring-Opitz syndrome (ASXL1) and Bainbridge-Ropers syndrome (ASXL3)
by: Maya C. Ayoub, et al.
Published: (2023-11-01)

Anesthetic experience for laparoscopic cholecystectomy in a patient with myelodysplastic syndrome with trisomy 8 mosaicism syndrome
by: Mae Hwa Kang, et al.
Published: (2014-12-01)

Usefulness of Adalimumab for Treating a Case of Intestinal Behçet's Disease With Trisomy 8 Myelodysplastic Syndrome
by: Masamichi Kimura, et al.
Published: (2015-04-01)

Prenatal diagnosis of low-level mosaicism for trisomy 21 with rare karyotype detected by noninvasive prenatal testing
by: Hong Wu, et al.
Published: (2017-10-01)

Premature ovarian failure related to trisomy X: Two case reports with an aberrant 47, XXX karyotype
by: Paresh Singhal, et al.
Published: (2021-01-01)

PB2013: THE FREQUENCY, EVOLUTION AND SIGNIFICANCE OF GENE MUTATION IN MYELODYSPLASTIC SYNDROMES WITH NORMAL KARYOTYPE
by: Feng Xu, et al.
Published: (2023-08-01)

PB1914: CYTOGENETIC FINDINGS IN 18 CHILDREN WITH MYELODYSPLASTIC SYNDROMES BY KARYOTYPIC AND FISH ANALYSIS
by: K. Manola, et al.
Published: (2022-06-01)

Regions of homozygosity confer a worse prognostic impact in myelodysplastic syndrome with normal karyotype
by: Mar Mallo, et al.
Published: (2023-05-01)

Assessing karyotype precision by microarray-based comparative genomic hybridization in the myelodysplastic/myeloproliferative syndromes
by: Forman Stephen J, et al.
Published: (2010-11-01)

Identifying the similarities and differences between single nucleotide polymorphism array (SNPa) analysis and karyotyping in acute myeloid leukemia and myelodysplastic syndromes
by: Thiago Rodrigo de Noronha, et al.
Published: (2015-02-01)

Experimental ASXL1‐Mediated Clonal Hematopoiesis Promotes Inflammation and Accelerates Heart Failure
by: Kyung‐Duk Min, et al.
Published: (2022-10-01)

ASXL1/2 mutations and myeloid malignancies
by: Edward A. Medina, et al.
Published: (2022-09-01)

Clonal evolution in myelodysplastic syndromes
by: Pedro da Silva-Coelho, et al.
Published: (2017-04-01)

An uncommon t(9;11)(p24;q22) with monoallelic loss of ATM and KMT2A genes in a child with myelodysplastic syndrome/acute myeloid leukemia who evolved from Fanconi anemia
by: Viviane Lamim Lovatel, et al.
Published: (2018-07-01)

P714: DISSECTING THE CLINICAL HETEROGENEITY OF ISOLATED TRISOMY 8 MYELODYSPLASTIC SYNDROMES THROUGH MUTATIONAL PROFILE
by: Sofía María Toribio Castelló, et al.
Published: (2023-08-01)

Mutational Profile Enables the Identification of a High-Risk Subgroup in Myelodysplastic Syndromes with Isolated Trisomy 8
by: Sofía Toribio-Castelló, et al.
Published: (2023-07-01)

Refractory Intestinal Behçet-Like Disease Associated with Trisomy 8 Myelodysplastic Syndrome Resolved by Parenteral Nutrition
by: Ryo Takahashi, et al.
Published: (2023-10-01)

Sole Infrequent Karyotypic Aberration Trisomy 6 in a Patient with Acute Myeloid Leukemia and Breast Cancer in Remission
by: Mürüvvet Seda Aydın, et al.
Published: (2017-03-01)

Next-generation Sequencing and Karyotype Analysis for the Diagnosis of Robertsonian Translocation Type Trisomy 13: A Case Report
by: Jing SHA, et al.
Published: (2017-05-01)

TP53 mutation status divides myelodysplastic syndromes with complex karyotypes into distinct prognostic subgroups
by: Haase, D, et al.
Published: (2019)