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免疫性涎腺炎(干燥综合征)中的淋巴瘤前期、早期淋巴瘤及明显淋巴瘤——一种淋巴瘤发生模型

Prelymphoma, early lymphoma, and manifest lymphoma in immunosialadenitis (Sjögren's syndrome)--a model of lymphomagenesis.

作者信息

Lennert K, Schmid U

出版信息

Haematol Blood Transfus. 1983;28:418-22. doi: 10.1007/978-3-642-68761-7_82.

Abstract

The development of malignant lymphoma in myoepithelial sialadenitis with and without Sjögren's syndrome was investigated. At first, prelymphomatous proliferation areas showing a polytypic immunoglobulin (Ig) pattern were seen. These transformed into malignant lymphoma with a monotypic Ig pattern, at first in small, circumscribed proliferation areas ("early lymphoma") and later in large, confluent proliferation area ("manifest lymphoma"). The lymphomas were classified as LP immunocytoma. In some cases they transformed into high-grade malignant lymphomas of the same category, namely, B-immunoblastic lymphoma. The same types of lymphoma have been found in NZB mice and chronic graft-versus-host reactions. "Primary" malignant lymphomas of salivary glands that did not show myoepithelial sialadenitis were also studied. These lymphomas were mostly germinal center cell tumors and probably developed primarily in lymph nodes within parotid glands in most, if not all, cases.

摘要

对伴有或不伴有干燥综合征的肌上皮涎腺炎中恶性淋巴瘤的发展情况进行了研究。起初,可见呈现多型免疫球蛋白(Ig)模式的淋巴瘤前期增殖区域。这些区域转变为具有单型Ig模式的恶性淋巴瘤,起初出现在小的、界限清楚的增殖区域(“早期淋巴瘤”),随后出现在大的、融合的增殖区域(“明显淋巴瘤”)。这些淋巴瘤被归类为淋巴浆细胞性免疫细胞瘤。在某些情况下,它们转变为同一类别的高级别恶性淋巴瘤,即B免疫母细胞淋巴瘤。在新西兰黑鼠和慢性移植物抗宿主反应中也发现了相同类型的淋巴瘤。还对未表现出肌上皮涎腺炎的涎腺“原发性”恶性淋巴瘤进行了研究。这些淋巴瘤大多为生发中心细胞肿瘤,在大多数(如果不是全部)病例中,可能主要起源于腮腺内的淋巴结。

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