Horny Hans-Peter, Sotlar Karl, Valent Peter
Institute of Pathology, Ansbach, Germany.
Pathobiology. 2007;74(2):121-32. doi: 10.1159/000101711.
Mastocytosis is a neoplastic disease involving mast cells (MC) and their CD34+ progenitors. Symptoms in mastocytosis are caused by biological mediators released from MC and/or the infiltration of neoplastic MC in various organs, the skin and the bone marrow being predominantly involved. A WHO consensus classification for mastocytosis exists, which is widely accepted and includes three major categories: (1) Cutaneous mastocytosis (CM), a benign disease in which MC infiltration is confined to the skin, is preferentially seen in young children and exhibits a marked tendency to regress spontaneously. (2) Systemic mastocytosis (SM) which is commonly diagnosed in adults and includes four major subtypes: (i) indolent SM (ISM, the most common form involving mainly skin and bone marrow); (ii) a unique subcategory termed SM with an associated non-mast cell clonal hematological disease (SM-AHNMD); (iii) aggressive SM usually presenting without skin lesions, and (iv) MC leukemia, probably representing the rarest variant of human leukemias. (3) The extremely rare localized extracutaneous MC neoplasms, either presenting as malignancy (MC sarcoma) or as benign tumor termed extracutaneous mastocytoma. Diagnostic criteria for mastocytosis are available and are widely accepted. SM criteria include one major criterion (multifocal compact tissue infiltration by MC) and four minor criteria: (1) prominent spindling of MC; (2) atypical immunophenotype of MC with coexpression of CD2 and/or CD25 (antigens which have not been found to be expressed on normal/reactive MC); (3) activating (somatic) point mutations of the c-kit proto-oncogene usually involving exon 17, with the imatinib-resistant type D816V being most frequent, and (4) persistently elevated serum tryptase level (>20 ng/ml). To establish the diagnosis of SM, at least one major and one minor criterion, or at least three minor criteria, have to be fulfilled. The natural clinical course of mastocytosis is variable. Most patients, in particular those with CM and ISM, remain in an indolent stage over many years or even decades, while others, in particular those with aggressive SM, SM-AHNMD, or mast cell leukemia, show a progressive course, usually with a fatal outcome.
肥大细胞增多症是一种涉及肥大细胞(MC)及其CD34 +祖细胞的肿瘤性疾病。肥大细胞增多症的症状是由MC释放的生物介质和/或肿瘤性MC在各个器官中的浸润引起的,主要累及皮肤和骨髓。世界卫生组织(WHO)对肥大细胞增多症有一个共识分类,该分类被广泛接受,包括三大类:(1)皮肤肥大细胞增多症(CM),一种良性疾病,其中MC浸润局限于皮肤,多见于幼儿,且有明显的自发消退倾向。(2)系统性肥大细胞增多症(SM),通常在成人中诊断,包括四个主要亚型:(i)惰性SM(ISM,最常见的形式,主要累及皮肤和骨髓);(ii)一个独特的亚类,称为伴有相关非肥大细胞克隆性血液病的SM(SM-AHNMD);(iii)侵袭性SM,通常无皮肤病变;(iv)肥大细胞白血病,可能是人类白血病中最罕见的变体。(3)极其罕见的局限性皮肤外MC肿瘤,可表现为恶性肿瘤(MC肉瘤)或称为皮肤外肥大细胞瘤的良性肿瘤。肥大细胞增多症的诊断标准是可用的且被广泛接受。SM标准包括一个主要标准(MC多灶性致密组织浸润)和四个次要标准:(一)MC显著梭形化;(二)MC的非典型免疫表型,伴有CD2和/或CD25共表达(这些抗原在正常/反应性MC上未被发现表达);(三)c-kit原癌基因的激活(体细胞)点突变,通常涉及外显子17,其中伊马替尼耐药型D816V最为常见;(四)血清类胰蛋白酶水平持续升高(>20 ng/ml)。要确立SM的诊断,必须满足至少一个主要标准和一个次要标准,或至少三个次要标准。肥大细胞增多症的自然临床病程各不相同。大多数患者,尤其是CM和ISM患者,多年甚至数十年都处于惰性阶段,而其他患者,尤其是侵袭性SM、SM-AHNMD或肥大细胞白血病患者,则呈现进行性病程,通常预后不良。