系统性肥大细胞增多症伴相关血液系统肿瘤。酪氨酸激酶抑制剂和异基因骨髓移植治疗的诊断特征和独特反应模式

Irene Hernández Alconchel , Sonia González de Villambrosía , Andrés Insunza Gaminde , Santiago Montes Moreno
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引用次数: 1

摘要

系统性肥大细胞增多症是肥大细胞的克隆性增殖;在相当一部分病例中,它与另一种并发的血液系统肿瘤有关。KIT突变和其他相关基因改变的分子分析表明,干细胞区室中有一个共同的起源。骨髓活检中的肥大细胞浸润模式在与t(8;21)AML相关的病例中可能是微妙的。在这里,我们报告了3例克隆相关的SM-AHN,2例SM-CMML和1例SM-t(8;21)AML。我们详细描述了异基因干细胞移植和新型TK抑制剂在诊断和治疗过程中的骨髓浸润模式,显示了治疗后肥大细胞清除的独特动态。
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Systemic Mastocytosis with Associated Hematological Neoplasms. Diagnostic features and unique response pattern to tyrosine kinase inhibitors and allo-bone marrow transplantation therapy

Systemic Mastocytosis is a clonal proliferation of mast cells; in a significant fraction of cases it is associated with another concurrent hematological neoplasm. Molecular analysis of KIT mutations and other associated genetic alterations suggest a common origin in the stem cell compartment. Mast cell infiltration patterns in bone marrow biopsy may be subtle in cases associated with t (8;21) AML. Here we report three cases of clonally related SM-AHN, two cases with SM-CMML and one case with SM- t (8;21) AML. We describe in detail the bone marrow infiltration pattern at diagnosis and during the course of treatment with allogeneic stem cell transplant and novel TK inhibitors, showing the unique dynamics of mast cell clearance after therapy.

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来源期刊
Revista Espanola de Patologia
Revista Espanola de Patologia Medicine-Pathology and Forensic Medicine
CiteScore
0.90
自引率
0.00%
发文量
53
审稿时长
34 days
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