Atlas of Genetics and Cytogenetics in Oncology and Haematology


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

X Y 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 16 17 18 19 20 21 22 NA

Childhood myelodysplastic syndromes

Clinics and Pathology

Disease very heterogeneous:

I- idiopathic MDS

II- secondary MDS: to previous chemo- and/or radio-therapy

III- 'genetic MDS': cases associated with a congenital genetic disease, such as:
-neurofibromatosis type 1 (Von Recklinhausen) (MIM 16220): an hamartoneoplastic syndrome Kostmann syndrome (MIM 20270): also called congenital neutropenia
-Bloom syndrome (MIM 21090): a chromosome instability syndrome Dubowitz syndrome (MIM 22337): mimicks Bloom's, but without chromosome instability
-Fanconi anaemia (MIM 22765): a chromosome instability syndrome
-Schwachman syndrome (MIM 26040): with pancreatic insufficiency, and risksof leukaemia
-Pearson disease (MIM 26056) and other mitochondrial diseases: they often share pancreatic insufficiency, bone marrow pancytopenia with myelodysplastic features but maintained polyclonality, muscular and other ubiquitous manifestations
-familial monosomy 7
-familial platelet storage pool deficiency
-unbalanced constitutional karyotypes, including +21, +8,del(11q), del(21q) miscellaneous conditions.

Phenotype / cell stem origin RA, RARS (very rare) , RAEB, RAEBT, CMML, 'Juvenile CML', 'Infantile Monosomy 7', 'non classifiable cases according to the FAB'; with variable proportions according to the studies
Epidemiology 10% of haematological malignancies in children; median age: 2 to 5 yrs; sex ratio: balanced for some, male predominance (in RAEB±T or CMML) for others
Prognosis CR is obtained; however, median survival is about 3 yrs, while 1/3 of the cases may be considered as cured; good prognostic features are: young age, female sex, normal karyotype, and some of the genetic predisposing factors; worse prognosis is found in secondary MDS, RAEB and RAEBT, cases with +8, +19, t(1;7).

Cytogenetics

Cytogenetics Morphological a normal karyotype or a monosomy 7 (intermediate prognosis) are found in 30% -or more- of cases each; others are: +8, +21, t(1;7), del(6q) ...

Bibliography

Myelodysplastic syndromes in childhood. Report of 21 patients from Italy and West Germany.
Creutzig U, Cantˆ¼-Rajnoldi A, Ritter J, Romitti L, Odenwald E, Conter V, Riehm H, Masera G
The American journal of pediatric hematology/oncology. 1987 ; 9 (4) : 324-330.
PMID 3439582
 
Childhood myelodysplasia: suggested classification as myelodysplastic syndromes based on laboratory and clinical findings.
Brandwein JM, Horsman DE, Eaves AC, Eaves CJ, Massing BG, Wadsworth LD, Rogers PC, Kalousek DK
The American journal of pediatric hematology/oncology. 1990 ; 12 (1) : 63-70.
PMID 2309981
 
Primary myelodysplastic syndrome in children: the clinical experience in 33 cases.
Tuncer MA, Pagliuca A, Hicsonmez G, Yetgin S, Ozsoylu S, Mufti GJ
British journal of haematology. 1992 ; 82 (2) : 347-353.
PMID 1419817
 
Myelodysplastic syndromes in childhood: a population based study of nine cases.
Hasle H, Jacobsen BB, Pedersen NT
British journal of haematology. 1992 ; 81 (4) : 495-498.
PMID 1390234
 
Analysis of karyotype, SCE, and point mutation of RAS oncogene in Indian MDS patients.
Mansoor AM, Bharadwaj TP, Sethuraman S, Chandy M, Pushpa V, Kamada N, Murthy PB
Cancer genetics and cytogenetics. 1993 ; 65 (1) : 12-20.
PMID 8431911
 
Myelodysplastic syndromes in childhood--classification, epidemiology, and treatment.
Hasle H
Leukemia & lymphoma. 1994 ; 13 (1-2) : 11-26.
PMID 8025513
 
Myelodysplasia and acute megakaryoblastic leukemia in Down's syndrome.
Zipursky A, Thorner P, De Harven E, Christensen H, Doyle J
Leukemia research. 1994 ; 18 (3) : 163-171.
PMID 8139285
 
Childhood myelodysplastic syndrome in Denmark: incidence and predisposing conditions.
Hasle H, Kerndrup G, Jacobsen BB
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K. 1995 ; 9 (9) : 1569-1572.
PMID 7658725
 
Pediatric myelodysplasia: a study of 68 children and a new prognostic scoring system.
Passmore SJ, Hann IM, Stiller CA, Ramani P, Swansbury GJ, Gibbons B, Reeves BR, Chessells JM
Blood. 1995 ; 85 (7) : 1742-1750.
PMID 7703482
 
Morphologic, immunologic, and cytogenetic classification of acute myeloid leukemia and myelodysplastic syndrome in childhood: a report from the Childrens Cancer Group.
Barnard DR, Kalousek DK, Wiersma SR, Lange BJ, Benjamin DR, Arthur DC, Buckley JD, Kobrinsky N, Neudorf S, Sanders J, Miller LP, Shina DC, Hammond GD, Woods WG
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K. 1996 ; 10 (1) : 5-12.
PMID 8558938
 
Forty-four cases of childhood myelodysplasia with cytogenetics, documented by the Groupe Franˆßais de Cytogˆ©nˆ©tique Hˆ©matologique.
Leukemia : official journal of the Leukemia Society of America, Leukemia Research Fund, U.K. 1997 ; 11 (9) : 1478-1485.
PMID 9305601
 
REVIEW articlesautomatic search in PubMed
Last year articlesautomatic search in PubMed

Contributor(s)

Written07-1997Jean-Loup Huret and Claude Léonard

Citation

This paper should be referenced as such :
Huret JL and Léonard C . Childhood myelodysplastic syndromes. Atlas Genet Cytogenet Oncol Haematol. July 1997 .
URL : http://AtlasGeneticsOncology.org/Anomalies/childMDS.html

The various updated versions of this paper are referenced and archived by INIST as such :
http://documents.irevues.inist.fr/bitstream/handle/2042/32022/07-1997-childMDS.pdf   [ Bibliographic record ]

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Fri Apr 18 14:10:05 CEST 2014


Home   Genes   Leukemias   Solid Tumours   Cancer-Prone   Deep Insight   Case Reports   Journals  Portal   Teaching   

For comments and suggestions or contributions, please contact us

jlhuret@AtlasGeneticsOncology.org.