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首页> 外文期刊>Southern Medical Journal >Angiotropic large cell lymphoma.
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Angiotropic large cell lymphoma.

机译:血管性大细胞淋巴瘤。

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摘要

Lymphomas are malignant neoplasms of cells native to lymphoid tissue that can arise anywhere in the body. Angiotropic large cell lymphoma (ALCL) is characterized by a proliferation of neoplastic mononuclear cells within the lumina of small blood vessels. The clinical manifestations are usually neurologic, including progressive dementia and nonlocalizing deficits, cutaneous infiltration, adrenal masses, or fever of unknown origin. The diagnosis is made at autopsy or on skin biopsy, brain biopsy, or other surgical resection. Differential diagnoses include metastatic malignant neoplasms and vascular tumors. We report the case of a 63-year-old white man who had neurologic signs and symptoms as well as dyspnea. Autopsy revealed ALCL involving multiple organ systems, including the central nervous system. Diagnostic techniques currently used to confirm the nature of this malignant neoplasm include immunohistochemistry, ultrastructural analysis, cytogenetics, and molecular biologic studies.
机译:淋巴瘤是淋巴组织固有的细胞恶性肿瘤,可在体内任何地方出现。血管性大细胞淋巴瘤(ALCL)的特征是小血管腔内肿瘤性单核细胞的增殖。临床表现通常是神经性的,包括进行性痴呆和非局部性缺陷,皮肤浸润,肾上腺肿块或不明原因的发烧。诊断是在尸体解剖或皮肤活检,脑活检或其他手术切除时做出的。鉴别诊断包括转移性恶性肿瘤和血管肿瘤。我们报告了一个63岁的白人患者的病例,该患者患有神经系统的体征和症状以及呼吸困难。尸检显示ALCL涉及多个器官系统,包括中枢神经系统。当前用于确认该恶性肿瘤性质的诊断技术包括免疫组织化学,超微结构分析,细胞遗传学和分子生物学研究。

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