PANCYTOPENIA AND VACUOLATION OF MARROW PRECURSORS ASSOCIATED WITH NECROTIZING ENCEPHALOPATHY

被引:9
作者
BLATT, J
KATERJI, A
BARMADA, M
WENGER, SL
PENCHANSKY, L
机构
[1] CHILDRENS HOSP PITTSBURGH,DEPT PEDIAT,DIV NEUROL,PITTSBURGH,PA 15213
[2] CHILDRENS HOSP PITTSBURGH,DEPT PEDIAT,DIV GENET,PITTSBURGH,PA 15213
[3] UNIV PITTSBURGH,SCH MED,DEPT PATHOL,DIV NEUROPATHOL,PITTSBURGH,PA
[4] UNIV PITTSBURGH,SCH MED,DEPT PATHOL,DIV HEMATOPATHOL,PITTSBURGH,PA
关键词
PANCYTOPENIA; SUBACUTE NECROTIZING ENCEPHALOPATHY; PEARSONS SYNDROME;
D O I
10.1111/j.1365-2141.1994.tb03280.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Subacute necrotizing encephalopathy (SNE) or Leigh disease is an autosomal recessive disorder associated with various defects of oxidative phosphorylation. Two reports have described the concurrence of SNE with pancytopenia and vacuolation of bone marrow precursors, and have raised the possibility that this symptom complex may be part of a spectrum of diseases which includes Pearson's syndrome (vacuolation of bone marrow precursors, sideroblastic anaemia, exocrine pancreatic dysfunction). We describe a case of Pearson's syndrome in which haematological manifestations antedated progressive neurological deterioration by several years. Cytogenetic studies showed an inverted duplication of chromosome 9 (qh) [inv dup (9) (qh)]. We suggest that cytopenia associated with vacuolation of bone marrow precursors even without clinically apparent central nervous system pathology should prompt consideration of SNE, or related diseases. Conversely, a diagnosis of SNE should prompt evaluation of other organ system functions including bone marrow. Cytogenetic evaluation of other patients with SNE may determine whether the 9 (qh) findings are pathogenetic.
引用
收藏
页码:207 / 209
页数:3
相关论文
共 12 条
[1]  
BERNARD J, 1962, NOUV REV FR HEMATOL, V2, P721
[2]   ASSOCIATION OF DIAMOND-BLACKFAN SYNDROME, PHYSICAL ABNORMALITIES, AND AN ABNORMALITY OF CHROMOSOME-1 [J].
HEYN, R ;
KURCZYNSKI, E ;
SCHMICKEL, R .
JOURNAL OF PEDIATRICS, 1974, 85 (04) :531-533
[3]  
LUBS HA, 1977, POPULATION CYTOGENET, P133
[4]   CONGENITAL HYPOPLASTIC-ANEMIA, DIABETES, AND SEVERE RENAL TUBULAR DYSFUNCTION ASSOCIATED WITH A MITOCHONDRIAL-DNA DELETION [J].
MAJANDER, A ;
SUOMALAINEN, A ;
VETTENRANTA, K ;
SARIOLA, H ;
PERKKIO, M ;
HOLMBERG, C ;
PIHKO, H .
PEDIATRIC RESEARCH, 1991, 30 (04) :327-330
[5]  
MCSHANE MA, 1991, AM J HUM GENET, V48, P39
[6]   NEW SYNDROME OF REFRACTORY SIDEROBLASTIC ANEMIA WITH VACUOLIZATION OF MARROW PRECURSORS AND EXOCRINE PANCREATIC DYSFUNCTION [J].
PEARSON, HA ;
LOBEL, JS ;
KOCOSHIS, SA ;
NAIMAN, JL ;
WINDMILLER, J ;
LAMMI, AT ;
HOFFMAN, R ;
MARSH, JC .
JOURNAL OF PEDIATRICS, 1979, 95 (06) :976-984
[7]  
Philippe N, 1971, Pediatrie, V26, P47
[8]  
ROTIG A, 1989, LANCET, V1, P902
[9]   SUBACUTE NECROTIZING ENCEPHALOPATHY - OXIDATIVE-PHOSPHORYLATION DEFECTS AND THE ATPASE 6 POINT MUTATION [J].
SHOFFNER, JM ;
FERNHOFF, PM ;
KRAWIECKI, NS ;
CAPLAN, DB ;
HOLT, PJ ;
KOONTZ, DA ;
TAKEI, Y ;
NEWMAN, NJ ;
ORTIZ, RG ;
POLAK, M ;
BALLINGER, SW ;
LOTT, MT ;
WALLACE, DC .
NEUROLOGY, 1992, 42 (11) :2168-2174
[10]  
SIMOPOULOS AP, 1972, NEUROLOGY, V22, P256