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源于黏膜相关淋巴组织的结外恶性淋巴瘤。

Extranodal malignant lymphoma arising from mucosa-associated lymphoid tissue.

作者信息

Isaacson P, Wright D H

出版信息

Cancer. 1984 Jun 1;53(11):2515-24. doi: 10.1002/1097-0142(19840601)53:11<2515::aid-cncr2820531125>3.0.co;2-c.

Abstract

Four cases of extranodal malignant lymphoma, one each arising in the stomach, salivary gland, lung, and thyroid, are described. These cases have many clinical, histopathologic, and immunohistochemical features in common, and it is proposed that this is because they share a common pattern of histogenesis from mucosa-associated lymphoid tissue (MALT). Clinical features of MALT-derived lymphomas include a tendency to remain localized for prolonged periods, and, thus, to be responsive to locally directed therapy. Histologically, this group of tumors is characterized by a noninvasive lymphoplasmacytic infiltrate within which foci of follicle center cells (FCC) can be seen invading epithelial structures, forming lymphoplasmacytic infiltrate lesions. Immunohistochemistry reveals monotypic cytoplasmic immunoglobulin (CIg) in the plasma cells serving to highlight the CIg-negative lymphoepithelial lesions. The clinical and histopathologic features of these lymphomas can be understood in the context of the behavioral characteristics and morphology of MALT.

摘要

本文描述了4例结外恶性淋巴瘤,分别起源于胃、唾液腺、肺和甲状腺。这些病例具有许多共同的临床、组织病理学和免疫组化特征,推测这是因为它们均起源于黏膜相关淋巴组织(MALT),具有共同的组织发生模式。MALT来源的淋巴瘤的临床特征包括倾向于长时间局限于局部,因此对局部治疗有反应。组织学上,这组肿瘤的特征是无侵袭性的淋巴浆细胞浸润,其中可见滤泡中心细胞(FCC)灶侵入上皮结构,形成淋巴浆细胞浸润性病变。免疫组化显示浆细胞内有单克隆胞质免疫球蛋白(CIg),有助于突出CIg阴性的淋巴上皮病变。这些淋巴瘤的临床和组织病理学特征可以从MALT的行为特征和形态学角度来理解。

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