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炎性肌成纤维细胞瘤:支持克隆起源的细胞遗传学证据。

Inflammatory myofibroblastic tumor: cytogenetic evidence supporting clonal origin.

作者信息

Su L D, Atayde-Perez A, Sheldon S, Fletcher J A, Weiss S W

机构信息

Department of Pathology, University of Michigan Hospitals, Ann Arbor 48105-0054, USA.

出版信息

Mod Pathol. 1998 Apr;11(4):364-8.

PMID:9578087
Abstract

The inflammatory myofibroblastic tumor (IMT) is a distinctive but controversial lesion, usually occurring during childhood, composed of fascicles of bland myofibroblastic cells admixed with a prominent inflammatory infiltrate consisting of lymphocytes, plasma cells, and eosinophils. Often affecting the lung and associated with constitutional symptoms, this lesion has been variously termed plasma cell granuloma, inflammatory pseudotumor, inflammatory myofibrohistiocytic proliferation, and inflammatory fibrosarcoma to reflect divergent views concerning its pathogenesis and level of malignancy. Cytogenetic analysis of an intra-abdominal myxoid hamartoma, a probable variant of this lesion, and a pulmonary IMT demonstrated clonal chromosomal abnormalities, lending support to the view that the IMT might be a neoplasm. There have been few cases studied to date, however, and the extent of cytogenetic anomalies in IMTs is not known. Karyotype analyses were performed on IMTs showing typical histologic features from three children. In addition, one case was studied by fluorescence in situ hybridization. Seventeen of 20 metaphase cells examined from a pulmonary IMT in a 5.5-year-old girl had an abnormal 47,XX+r(ring) karyotype. Fluorescence in situ hybridization studies demonstrated that the ring chromosome contained sequences of chromosome 8. Of 40 metaphase cells studied from a mesenteric IMT in an 8-month-old boy, 12 showed clonal aberrations, characterized as 43,XY,add(1)(p36),add(2)(p24),-6,der(14,22)(q10;q10),-19. Each of 20 metaphase cells examined from a retroperitoneal IMT in a 14-year-old girl contained complex clonal and nonclonal aberrations, characterized as 46-47,X,-X,add(2)(p22),add(2)(q13),+add(2)(q13),+5,-6,+i(7)(p10),add(8)( p11.2),+del(9)(p13),add(11)(p11.2)add(11)(q25),-13,-16,-18,add(19)(q13.1 ),add(19)(q13.1),+20,-21,-22,+mar1,+1-2mars. The presence of clonal chromosomal aberrations in all of the three tumors indicates that the IMT is a neoplastic proliferation.

摘要

炎性肌纤维母细胞瘤(IMT)是一种独特但存在争议的病变,通常发生于儿童期,由温和的肌纤维母细胞束组成,并伴有由淋巴细胞、浆细胞和嗜酸性粒细胞构成的显著炎性浸润。该病变常累及肺部并伴有全身症状,曾被赋予多种不同名称,如浆细胞性肉芽肿、炎性假瘤、炎性肌纤维组织细胞增生及炎性纤维肉瘤,以反映关于其发病机制和恶性程度的不同观点。对一例腹腔黏液样错构瘤(该病变可能的一种变体)及一例肺部IMT进行细胞遗传学分析,结果显示存在克隆性染色体异常,这支持了IMT可能是一种肿瘤的观点。然而,迄今为止研究的病例很少,IMT中细胞遗传学异常的程度尚不清楚。对三名儿童具有典型组织学特征的IMT进行了核型分析。此外,对一例病例进行了荧光原位杂交研究。在一名5.5岁女孩的肺部IMT检查的20个中期细胞中,有17个具有异常的47,XX+r(环状)核型。荧光原位杂交研究表明,环状染色体包含8号染色体的序列。在一名8个月大男孩的肠系膜IMT研究的40个中期细胞中,有12个显示出克隆性畸变,特征为43,XY,add(1)(p36),add(2)(p24),-6,der(14,22)(q10;q10),-19。在一名14岁女孩的腹膜后IMT检查的20个中期细胞中,每个细胞都包含复杂的克隆性和非克隆性畸变,特征为46 - 47,X,-X,add(2)(p22),add(2)(q13),+add(2)(q13),+5,-6,+i(7)(p10),add(8)(p11.2),+del(9)(p13),add(11)(p11.2)add(11)(q25),-13,-16,-18,add(19)(q13.1),add(19)(q13.1),+20,-21,-22,+mar1,+1 - 2mars。这三个肿瘤中均存在克隆性染色体畸变,表明IMT是一种肿瘤性增殖。

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