期刊
HAEMATOLOGICA-THE HEMATOLOGY JOURNAL
卷 97, 期 9, 页码 1312-1319出版社
FERRATA STORTI FOUNDATION
DOI: 10.3324/haematol.2011.057489
关键词
Shwachman-Diamond syndrome; genotype; aplastic anemia; secondary leukemia; cytopenia; myelodysplasia; monosomy 7
类别
资金
- Amgen SAS
- Chugai SA
- GIS Maladies Rares
- Institut de Veille Sanitaire
- Inserm
- Association Laurette Fugain
- Association Sportive de Saint Quentin Fallavier
- IRIS association
- Societe d'Hemato Immunologie Pediatrique
Background Patients with the Shwachman-Diamond syndrome often develop hematologic complications. No risk factors for these complications have so far been identified. The aim of this study was to classify the hematologic complications occurring in patients with Shwachman-Diamond syndrome and to investigate the risk factors for these complications. Design and Methods One hundred and two patients with Shwachman-Diamond syndrome, with a median follow-up of 11.6 years, were studied. Major hematologic complications were considered in the case of definitive severe cytopenia (i.e. anemia <7 g/dL or thrombocytopenia <20x10(9)/L), classified as malignant (myelodysplasia/leukemia) according to the 2008 World Health Organization classification or as non-malignant. Results Severe cytopenia was observed in 21 patients and classified as malignant severe cytopenia (n=9), non-malignant severe cytopenia (n=9) and malignant severe cytopenia preceded by nonmalignant severe cytopenia (n=3). The 20-year cumulative risk of severe cytopenia was 24.3% (95% confidence interval: 15.3%-38.5%). Young age at first symptoms (<3 months) and low hematologic parameters both at diagnosis of the disease and during the follow-up were associated with severe hematologic complications (P<0.001). Fifteen novel SBDS mutations were identified. Genotype analysis showed no discernible prognostic value. Conclusions Patients with Shwachman-Diamond syndrome with very early symptoms or cytopenia at diagnosis (even mild anemia or thrombocytopenia) should be considered at a high risk of severe hematologic complications, malignant or non-malignant. Transient severe cytopenia or an indolent cytogenetic clone had no deleterious value.
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