Improved neutrophil function in a glycogen storage disease type 1b patient after liver transplantation

被引:21
作者
Adachi, M
Shinkai, M
Ohhama, Y
Tachibana, K
Kuratsuji, T
Saji, H
Maruya, E
机构
[1] Kanagawa Childrens Med Ctr, Dept Endocrinol & Metab, Minami Ku, Yokohama, Kanagawa 2328555, Japan
[2] Kanagawa Childrens Med Ctr, Dept Surg, Yokohama, Kanagawa 2328555, Japan
[3] Int Med Ctr Japan, Res Inst, Tokyo, Japan
[4] NPO HLA Lab, Kyoto, Japan
关键词
cytotoxicity; G6PT gene; granulopenia; neutropenia; phagocytic activity;
D O I
10.1007/s00431-004-1405-1
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Patients with glycogen storage disease type 1b (GSD1b) not only show hepatomegaly, hypoglycaemia and lactic acidosis, but also neutropenia and neutrophil dysfunction. Here, we report improvement of neutropenia and neutrophil function in a 22-year-old male GSD1b patient who had undergone living-related partial liver transplantation (LT) at 18 years of age. After LT, the patient's infectious episodes decreased, gastrointestinal symptoms ameliorated, neutrophil counts increased, and neutrophil function tests normalised. Conclusion:although it is not known whether this improvement was causally related to liver transplantation, this may be the first recorded case of restoration of neutrophil dysfunction in a glycogen storage disease type 1b patient.
引用
收藏
页码:202 / 206
页数:5
相关论文
共 24 条
[1]  
BASS DA, 1983, J IMMUNOL, V130, P1910
[2]  
DUNN PA, 1981, J LAB CLIN MED, V98, P374
[3]  
Fernandes J, 2000, INBORN METABOLIC DIS, P85
[4]   Inactivation of the glucose 6-phosphate transporter causes glycogen storage disease type 1b [J].
Hiraiwa, H ;
Pan, CJ ;
Lin, BC ;
Moses, SW ;
Chou, JY .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (09) :5532-5536
[5]  
Hou DC, 1999, AM J MED GENET, V86, P253, DOI 10.1002/(SICI)1096-8628(19990917)86:3<253::AID-AJMG11>3.0.CO
[6]  
2-7
[7]   SUPEROXIDE ANION PRODUCTION AND EXPRESSION OF CYTOCHROME-B558 BY NEUTROPHILS ARE IMPAIRED IN SOME PATIENTS WITH MYELODYSPLASTIC SYNDROME [J].
ITOH, Y ;
KURATSUJI, T ;
AIZAWA, S ;
SAI, M ;
OHYASHIKI, K ;
TOYAMA, K .
ANNALS OF HEMATOLOGY, 1991, 63 (05) :270-275
[8]  
ITOH Y, 1991, INT J HEMATOL, V54, P463
[9]   Molecular analysis of glycogen storage disease type Ib: Identification of a prevalent mutation among Japanese patients and assignment of a putative glucose-6-phosphate translocase gene to chromosome 11 [J].
Kure, S ;
Suzaki, Y ;
Matsubara, Y ;
Sakamoto, O ;
Shintaku, H ;
Isshiki, G ;
Hoshida, C ;
Izumi, I ;
Sakura, N ;
Narisawa, K .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 1998, 248 (02) :426-431
[10]   Glycogen storage disease type Ib without neutropenia [J].
Kure, S ;
Hou, DC ;
Suzuki, Y ;
Yamagishi, A ;
Hiratsuka, M ;
Fukuda, T ;
Sugie, H ;
Kondo, N ;
Matsubara, Y ;
Narisawa, K .
JOURNAL OF PEDIATRICS, 2000, 137 (02) :253-256