Literature DB >> 12959859

Transient myelodysplastic syndrome associated with isochromosome 7q abnormality.

Elaine W Leung1, Richard C Woodman, Birgitte Roland, Mohamed Abdelhaleem, Melvin H Freedman, Yigal Dror.   

Abstract

Myelodysplastic syndrome (MDS) in childhood is a rare hematological condition that is often associated with cytogenetic abnormalities, the most common being monosomy 7/del(7q). The clinical course of MDS can vary from stable disease to rapid progression into acute leukemia. Rarely, spontaneous remission of MDS has been observed. The authors report the first case of a transient MDS associated with a clonal marrow cytogenetic abnormality consisting of isochromosome 7q in a previously well child. Without intervention, the bone marrow cytogenetics reverted to normal and there was complete hematologic recovery. This case illustrates the importance of close follow-up in a child presenting with MDS, to detect spontaneous recovery or evolution of the disease.

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Year:  2003        PMID: 12959859     DOI: 10.1080/08880010390232754

Source DB:  PubMed          Journal:  Pediatr Hematol Oncol        ISSN: 0888-0018            Impact factor:   1.969


  4 in total

1.  Patients with spontaneous remission of high-risk MDS and AML show persistent preleukemic clonal hematopoiesis.

Authors:  Victoria V Grunwald; Marcus Hentrich; Xaver Schiel; Annika Dufour; Stephanie Schneider; Michaela Neusser; Marion Subklewe; Michael Fiegl; Wolfgang Hiddemann; Karsten Spiekermann; Maja Rothenberg-Thurley; Klaus H Metzeler
Journal:  Blood Adv       Date:  2019-09-24

2.  Spontaneous remission of 2-chlorodeoxyadenosine (2-CdA)-related secondary myelodysplastic syndrome in a patient with refractory Langerhans cell histiocytosis.

Authors:  Daisuke Suzuki; Ryoji Kobayashi; Hirozumi Sano; Kenji Kishimoto; Kazue Yasuda; Masanori Nakanishi; Tetsuro Nagashima; Kunihiko Kobayashi
Journal:  Int J Hematol       Date:  2013-04-25       Impact factor: 2.490

3.  Spontaneous remission in adults with primary myelodysplastic syndromes: incidence and characteristics of patients.

Authors:  Dragomir Marisavljević; Zoran Rolović; Milena Ludoski-Pantić; Vesna Djordjević; Angelina Novak
Journal:  Med Oncol       Date:  2005       Impact factor: 3.738

4.  Constitutional SAMD9L mutations cause familial myelodysplastic syndrome and transient monosomy 7.

Authors:  Victor B Pastor; Sushree S Sahoo; Jessica Boklan; Georg C Schwabe; Ebru Saribeyoglu; Brigitte Strahm; Dirk Lebrecht; Matthias Voss; Yenan T Bryceson; Miriam Erlacher; Gerhard Ehninger; Marena Niewisch; Brigitte Schlegelberger; Irith Baumann; John C Achermann; Akiko Shimamura; Jochen Hochrein; Ulf Tedgård; Lars Nilsson; Henrik Hasle; Melanie Boerries; Hauke Busch; Charlotte M Niemeyer; Marcin W Wlodarski
Journal:  Haematologica       Date:  2017-12-07       Impact factor: 9.941

  4 in total

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