Detection of c-kit point mutation Asp-816 → Val in microdissected pooled single mast cells and leukemic cells in a patient with systemic mastocytosis and concomitant chronic myelomonocytic leukemia

被引:58
作者
Sotlar, K
Fridrich, C
Mall, A
Jaussi, R
Bültmann, B
Valent, P
Horny, HP
机构
[1] Univ Tubingen, Inst Pathol, D-72076 Tubingen, Germany
[2] Univ Cologne, Inst Pathol, D-5000 Cologne, Germany
[3] Univ Vienna, Dept Internal Med 1, Div Hematol & Hemostaseol, Vienna, Austria
[4] Med Univ Lubeck, Inst Pathol, MUL, D-23538 Lubeck, Germany
关键词
mast cells; microdissection; c-kit; point mutation; tryptase;
D O I
10.1016/S0145-2126(02)00041-3
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
The c-kit mutation Asp-816 --> Val is detectable not only in neoplastic mast cells (MCs) in patients with systemic mastocytosis (SM) but also in most associated hematologic non-MC lineage disease (AHNMD). In order to prove a monoclonal disease evolution we investigated DNA of pooled microdissected single cells for the presence of the mutation in a patient with SM and concomitant chronic myelomonocytic leukemia (CMML). LightCycler melting curve analysis and direct sequencing of nested polymerase chain reaction (PCR) products revealed the c-kit mutation in tryptase-positive MC and in leukemic CD15-positive cells in bone marrow infiltrates, but not in colonic epithelial cells, thus, suggesting a monoclonal evolution of SM and concurrent CMML on the basis of a somatic mutation in a common hematologic progenitor. (C) 2002 Elsevier Science Ltd. All rights reserved.
引用
收藏
页码:979 / 984
页数:6
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