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Fanconi anemia: a single center experience of a large cohort
- Source :
- The Turkish Journal of Pediatrics. 61:477
- Publication Year :
- 2019
- Publisher :
- The Turkish Journal of Pediatrics, 2019.
-
Abstract
- Kesici S, Unal S, Kuskonmaz B, Aytac S, Cetin M, Gumruk F. Fanconi anemia: a single center experience of a large cohort. Turk J Pediatr 2019; 61: 477-484. Fanconi anemia (FA) is an inherited disease, characterized by congenital malformations, short stature, progressive bone marrow failure and predisposition to leukemia and solid tumors. The aim of this study was to evaluate the clinical and prognostic features of FA patients followed in a single center. The charts of FA patients were reviewed 35 years retrospectively and a total of 175 patients were included in the study in which 51.4% of patients were male. The mean age at diagnosis was 6.3±4.1 years. The incidence of microcephaly was 92.6%, skin findings were 88.0%, eye abnormality was 74.3%, thumb and radius abnormality was 53.1%, urinary system abnormality was 30.9%, skeletal system abnormality other than thumb and radius was 18.9%, genital system abnormality was 11.4%, cardiovascular system abnormality was 11.4%, ear and hearing abnormalities were 9.7% and gastrointestinal system abnormality was 5.7%. Short stature was present in 75.4% of the patients. Of the 175 patients 167 (95.4%) developed bone marrow failure during follow-up and the mean age of bone marrow failure was 7.1 ±3.7 years (1 month-old-19.8 years). The first clinical symptom was thrombocytopenia in 83.4% of patients. Malignancy developed in a total of 23 (13.1 %) patients (20 leukemia, 3 solid tumors) during follow-up. Of 175 patients, 35 (20%) underwent hematopoietic stem cell transplantation. Fatality rate among patients who underwent hematopoietic stem cell transplantation was 31.4% (11/35) and fatality rate among other patients was 63.4% (83/131; p < 0.05). Of 94 patients who deceased, death was due to bleeding in 44.7%, infection in 34%, leukemia progression in 16.0% and graft versus host disease in 5.3%. In terms of the number of patients included, this study is one of the largest cohorts with a remarkable duration of follow-up time. Hematopoietic stem cell transplantation was found to have a good impact on sur vival of patients.
- Subjects :
- Male
medicine.medical_specialty
Adolescent
medicine.medical_treatment
Hematopoietic stem cell transplantation
Single Center
Short stature
Gastroenterology
Young Adult
03 medical and health sciences
0302 clinical medicine
Fanconi anemia
030225 pediatrics
Internal medicine
Case fatality rate
medicine
Humans
Child
Retrospective Studies
business.industry
Hematopoietic Stem Cell Transplantation
Bone marrow failure
Infant
Prognosis
medicine.disease
Leukemia
Child, Preschool
Pediatrics, Perinatology and Child Health
Disease Progression
Female
medicine.symptom
Abnormality
business
030217 neurology & neurosurgery
Follow-Up Studies
Subjects
Details
- ISSN :
- 00414301
- Volume :
- 61
- Database :
- OpenAIRE
- Journal :
- The Turkish Journal of Pediatrics
- Accession number :
- edsair.doi.dedup.....d908c501f916d3d01b162fba1805d683