A Clinical Study on Myelodysplastic Syndrome in Childhood.
- Author:
Jun Eun PARK
1
;
Jong Jin SEO
;
Hyung Nam MOON
;
Chan Jung PARK
;
Hyun Sook CHI
;
Thad GHIM
Author Information
1. Department of Pediatrics, University of Ulsan, College of Medicine, Seoul, Korea. jjseo@www.amc.seoul.kr
- Publication Type:Original Article
- Keywords:
Childhood myelodysplastic syndrome;
Prognosis;
FAB;
International prognostic scoring system
- MeSH:
Anemia, Refractory;
Anemia, Refractory, with Excess of Blasts;
Child;
Chungcheongnam-do;
Diagnosis;
Education;
Fever;
Hemorrhage;
Humans;
Leukemia, Myelomonocytic, Juvenile;
Lymphatic Diseases;
Myelodysplastic Syndromes*;
Neutrophils;
Pallor;
Pancytopenia;
Prognosis;
Retrospective Studies;
Thrombocytopenia
- From:Korean Journal of Pediatric Hematology-Oncology
1999;6(2):250-258
- CountryRepublic of Korea
- Language:Korean
-
Abstract:
PURPOSE: This study was undertaken to investigate the clinical characteristics and prognostic predictors of myelodysplastic syndrome (MDS) in childhood. Method: The characteristics and laboratory findings of 20 patients seen at Asan Medical Center for the past 10 years from September 1989 to August 1998 were reviewed retrospectively with regard to the new International Prognostic Scoring System (IPSS) proposed by International MDS Risk Analysis Workshop. RESULTS: 1) In 20 children with MDS we studied, there was no age or sex predilection unique to the subgroups of MDS. 2) 19 cases (95%) out of the 20 had pallor at the time of diagnosis. Other major clinical findings were bleeding tendency in 11 (55%), fever in 8 (40%), hepatosplenomegaly in 8 (40%), and lymphadenopathy in 3 (15%). 3) The hemoglobin level was less than 10 g/dL in all cases and absolute neutrophil count (ANC) was decreased in 11 cases, thrombocytopenia in 15 cases. Pancytopenia was noted in 8 cases (40%). 4) Of the 20 cases, 9 had refractory anemia (RA), 3 refractory anemia with excess blasts (RAEB), 3 refractory anemia with excess blasts in transformation (RAEBIT), and 5 juvenile chronic myelogenous leukemia (JCML). 5) All RA patients were Intermediate (INT)-1 risk group, and all RAEB children were INT-2 risk group. The 3 cases of RAEBIT fell into INT-1, INT-2, and high risk group. Three cases of JCML were INT-1 group, and 2 cases INT-2 group. 6) Seven cases out of 13 INT-1 group had mean survival of 20.2 month (6~57 month), but only 1 out of 6 INT-2 survived. One case of high risk group succumbed to disease 50 months after diagnosis. CONCLUSION: These results showed that there was no age or sex predilection for the specific subgroup of childhood MDS. All the FAB subtypes of the childhood MDS except RA subgroup had poor survival. In this study, we found the IPSS seemed to be a prognostic predictor in childhood MDS but more cases are needed to confirm the validity of IPSS.
