CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II DIAGNOSED IN A 69-YEAR-OLD PATIENT WITH IRON OVERLOAD

被引：15

作者：

GREINER, TC

BURNS, CP

DICK, FR

HENRY, KM

MAHMOOD, I

机构：

[1] UNIV IOWA,COLL MED,DEPT PATHOL,IOWA CITY,IA 52242

[2] UNIV IOWA,COLL MED,DEPT INTERNAL MED,IOWA CITY,IA 52242

来源：

AMERICAN JOURNAL OF CLINICAL PATHOLOGY | 1992年 / 98卷 / 05期

关键词：

D O I：

10.1093/ajcp/98.5.522

中图分类号：

R36 [病理学];

学科分类号：

100104 ;

摘要：

Congenital dyserythropoietic anemia type II is a rare disorder that is often diagnosed in patients before age 20 years. Patients with this disorder, which is also called hereditary erythroblastic multinuclearity associated with a positive acidified serum lysis test, may have symptoms of iron overload. The purpose of this case report is to alert physicians to consider the diagnosis of congenital dyserythropoietic anemia type II in elderly patients who have anemia and iron overload.

引用

收藏

页码：522 / 525

页数：4

相关论文

共 19 条

[1] PROPOSALS FOR THE CLASSIFICATION OF THE MYELODYSPLASTIC SYNDROMES [J].

BENNETT, JM ;

CATOVSKY, D ;

DANIEL, MT ;

FLANDRIN, G ;

GALTON, DAG ;

GRALNICK, HR ;

SULTAN, C .

BRITISH JOURNAL OF HAEMATOLOGY, 1982, 51 (02) :189-199

[2] CONGENITAL DYSERYTHROPOIETIC ANEMIA (TYPE-II) PRESENTING WITH HEMOSIDEROSIS [J].

BIRD, AR ;

JACOBS, P ;

MOORES, P .

ACTA HAEMATOLOGICA, 1987, 78 (01) :33-36

[3] IRON LOADING IN CONGENITAL DYSERYTHROPOIETIC ANEMIAS AND CONGENITAL SIDEROBLASTIC ANEMIAS [J].

CAZZOLA, M ;

BAROSI, G ;

BERGAMASCHI, G ;

DEZZA, L ;

PALESTRA, P ;

POLINO, G ;

RAMELLA, S ;

SPRIANO, P ;

ASCARI, E .

BRITISH JOURNAL OF HAEMATOLOGY, 1983, 54 (04) :649-654

[4] HEREDITARY ERYTHROBLASTIC MULTINUCLEARITY ASSOCIATED WITH A POSITIVE ACIDIFIED-SERUM TEST - A TYPE OF CONGENITAL DYSERYTHROPOIETIC ANAEMIA [J].

CROOKSTON, JH ;

CROOKSTON, MC ;

BURNIE, KL ;

FRANCOMBE, WH ;

DACIE, JV ;

DAVIS, JA ;

LEWIS, SM .

BRITISH JOURNAL OF HAEMATOLOGY, 1969, 17 (01) :11-+

[5] TYPE-II CONGENITAL DYSERYTHROPOIETIC ANEMIA [J].

ENQUIST, RW ;

GOCKERMA.JP ;

DILLON, DE ;

WARKEL, RL ;

JENIS, EH .

ANNALS OF INTERNAL MEDICINE, 1972, 77 (03) :371-+

[6]

FUKUDA M N, 1990, Glycobiology, V1, P9, DOI 10.1093/glycob/1.1.9

[7] INCOMPLETE SYNTHESIS OF N-GLYCANS IN CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II CAUSED BY A DEFECT IN THE GENE ENCODING ALPHA-MANNOSIDASE-II [J].

FUKUDA, MN ;

MASRI, KA ;

DELL, A ;

LUZZATTO, L ;

MOREMEN, KW .

PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (19) :7443-7447

[8]

FUKUDA MN, 1987, J BIOL CHEM, V262, P7195

[9] CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-II (HEMPAS) - CHARACTERIZATION OF ABERRANT INTRACELLULAR ORGANELLES BY IMMUNOGOLD ELECTRON-MICROSCOPY [J].

FUKUDA, MN ;

KLIER, G ;

SCARTEZZINI, P .

BRITISH JOURNAL OF HAEMATOLOGY, 1987, 67 (01) :95-101

[10] SEVERE HEMOCHROMATOSIS - THE PREDOMINANT CLINICAL MANIFESTATION OF CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE-2 [J].

HALPERN, Z ;

RAHMANI, R ;

LEVO, Y .

ACTA HAEMATOLOGICA, 1985, 74 (03) :178-180