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与恶性组织细胞相比,恶性纤维组织细胞瘤及其他软组织肿瘤中肿瘤细胞的特征。I. 石蜡切片的免疫组织化学研究

Characterization of tumour cells in malignant fibrous histiocytomas and other soft tissue tumours in comparison with malignant histiocytes. I. Immunohistochemical study on paraffin sections.

作者信息

Roholl P J, Kleyne J, Elbers H, Van der Vegt M C, Albus-Lutter C, Van Unnik J A

出版信息

J Pathol. 1985 Oct;147(2):87-95. doi: 10.1002/path.1711470203.

DOI:10.1002/path.1711470203
PMID:2999365
Abstract

We have studied the possible origin of histiocytic cells, present in fibrous histiocytomas (MFH) by using immunohistochemistry to demonstrate lysozyme, alpha 1-antitrypsin, alpha 1-antichymotrypsin and receptors for peanut and soy bean agglutinin in tumour cells of MFH compared with their presence in tumour cells of malignant histiocytosis (MH) ('true' histiocytic lymphoma, 'true' histiocytic sarcoma). We included in this study a number of other soft tissue tumours (STT). Lysozyme was detected in half of the cases of malignant histiocytosis (n = 16) but in only two out of 77 MFH. alpha 1-Antitrypsin and alpha 1-antichymotrypsin usually occurred together although the latter was seen in more cases. Both markers were present in majority of cases of MH whereas they were detected in a minority of cases of MFH. MFH cases of the storiform subtype were less frequently stained than the pleomorphic or giant cell subtypes. Receptors for peanut or soy bean agglutinin were detected in nearly all MH cases, whereas their presence was only detected in a small number of MFH. Lysozyme was not detectable in other STT. alpha 1-Antitrypsin and alpha 1-antichymotrypsin were uncommonly present in other STT, except in osteosarcoma and rhabdomyosarcoma. These markers therefore have a limited value as indicators of a possible histiocytic origin of MFH. Lectins showed weak affinity for other STT. In accordance with others, we therefore conclude that the progenitor cell of MFH has to be sought within the undifferentiated mesenchymal cells and that histiocytes themselves probably do not give rise to MFH.

摘要

我们通过免疫组织化学方法,检测纤维组织细胞瘤(MFH)肿瘤细胞中溶菌酶、α1-抗胰蛋白酶、α1-抗糜蛋白酶以及花生凝集素和大豆凝集素受体,与恶性组织细胞增多症(MH)(“真性”组织细胞淋巴瘤、“真性”组织细胞肉瘤)肿瘤细胞中这些物质的情况进行比较,研究了MFH中组织细胞的可能来源。本研究还纳入了一些其他软组织肿瘤(STT)。在半数恶性组织细胞增多症病例(n = 16)中检测到溶菌酶,但在77例MFH中仅2例检测到。α1-抗胰蛋白酶和α1-抗糜蛋白酶通常同时出现,不过后者出现的病例更多。这两种标志物在大多数MH病例中存在,而在少数MFH病例中被检测到。席纹状亚型的MFH病例染色频率低于多形性或巨细胞亚型。几乎所有MH病例中都检测到花生凝集素或大豆凝集素受体,而在少数MFH中才检测到它们的存在。在其他STT中未检测到溶菌酶。α1-抗胰蛋白酶和α1-抗糜蛋白酶在其他STT中很少出现,除了骨肉瘤和横纹肌肉瘤。因此,这些标志物作为MFH可能组织细胞起源的指标价值有限。凝集素对其他STT显示出弱亲和力。因此,与其他人的观点一致,我们得出结论,MFH的祖细胞必须在未分化的间充质细胞中寻找,组织细胞本身可能不会产生MFH。

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引用本文的文献

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Does the pleomorphic xanthoastrocytoma exist? Problems in the application of immunological techniques to the classification of brain tumors.多形性黄色星形细胞瘤是否存在?免疫技术在脑肿瘤分类应用中的问题。
Acta Neuropathol. 1988;76(3):245-52. doi: 10.1007/BF00687771.
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Case report 444. Subperiosteal malignant fibrous histocytoma (MFH) of thigh, with involvement of femur.
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Malignant fibrous histiocytoma. Evidence of perivascular mesenchymal cell origin immunocytochemical studies with monoclonal anti-MFH antibodies.恶性纤维组织细胞瘤。血管周围间充质细胞起源的证据:用单克隆抗恶性纤维组织细胞瘤抗体进行免疫细胞化学研究。
Am J Pathol. 1987 Sep;128(3):528-37.
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Gliosarcoma: an immunohistochemical study.胶质肉瘤:一项免疫组织化学研究。
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Malignant fibrous histiocytoma.恶性纤维组织细胞瘤
Postgrad Med J. 1989 Dec;65(770):872-4. doi: 10.1136/pgmj.65.770.872.
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Malignant fibrous histiocytoma: similarities to the "fibrohistiocytoid cells" in chronic inflammation.恶性纤维组织细胞瘤:与慢性炎症中的“纤维组织细胞样细胞”的相似性。
Virchows Arch A Pathol Anat Histopathol. 1989;414(4):285-98. doi: 10.1007/BF00734082.
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