Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters











Database
Publication year range
1.
Int J Hematol ; 99(2): 154-61, 2014 Feb.
Article in English | MEDLINE | ID: mdl-24338744

ABSTRACT

Transient abnormal myelopoiesis (TAM) in neonates with Down syndrome (DS) is characterized by the transient appearance of blast cells, which resolves spontaneously. Approximately 20 % of patients with TAM die at an early age due to organ failure, including liver disease. We studied 25 DS-TAM patients retrospectively to clarify the correlation between clinical and laboratory characteristics and liver diseases. Early death (<6 months of age) occurred in four of the 25 patients (16.0 %), and two of those four patients died due to liver failure. Although physiologic jaundice improved gradually after a week, all DS patients had elevated D-Bil levels during the clinical course of TAM, except one who suffered early death. The median peak day of the WBC count, total bilirubin (T-Bil) and D-Bil levels was: day 1 (range day 0-57), day 8 (range day 1-55), and day 17 (range 1-53), respectively. Our results reveal that all patients with DS-TAM may develop liver disease irrespective of the absence or presence of symptoms and risk factors for early death. In patients of DS-TAM, careful observation of the level of D-Bil is needed by at least 1 month of age for the detection of liver disease risk.


Subject(s)
Down Syndrome/physiopathology , Hepatic Insufficiency/etiology , Leukemoid Reaction/physiopathology , Liver/physiopathology , Disease Progression , Female , Hepatic Insufficiency/congenital , Hepatic Insufficiency/epidemiology , Hepatic Insufficiency/physiopathology , Hospitals, Pediatric , Humans , Infant, Newborn , Japan/epidemiology , Male , Multiple Organ Failure/epidemiology , Multiple Organ Failure/etiology , Retrospective Studies , Risk Factors , Severity of Illness Index
2.
Rinsho Ketsueki ; 48(2): 140-3, 2007 Feb.
Article in Japanese | MEDLINE | ID: mdl-17370642

ABSTRACT

We report on a case of pediatric acute lymphoblastic leukemia presenting with massive bone marrow necrosis. A 4-year-old boy complained of fever and leg pain. Laboratory data revealed pancytopenia, but bone marrow examination showed only necrotic materials. About one month later, repeated bone marrow examination showed leukemic cells and the necrotic marrow had disappeared. The patient was treated with standard chemotherapy and was successfully induced to complete remission. Patients with massive bone marrow necrosis should undergo bone marrow examination repeatedly to make the correct diagnosis.


Subject(s)
Bone Marrow Diseases/etiology , Bone Marrow/pathology , Precursor Cell Lymphoblastic Leukemia-Lymphoma/complications , Precursor Cell Lymphoblastic Leukemia-Lymphoma/diagnosis , Bone Marrow Diseases/pathology , Child, Preschool , Diagnosis, Differential , Humans , Male , Necrosis , Precursor Cell Lymphoblastic Leukemia-Lymphoma/drug therapy , Precursor Cell Lymphoblastic Leukemia-Lymphoma/pathology , Remission Induction
SELECTION OF CITATIONS
SEARCH DETAIL