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成人口腔中非典型柏奇特氏淋巴瘤-類柏奇特氏淋巴瘤-病例報告

Adult Atypical/Burkitt-like Lymphoma in Oral Cavity-A Case Report

摘要


柏奇特氏淋巴瘤源於B細胞癌化增生,是一種高度惡性的非霍金氏淋巴瘤。它的疾病發生率很低,在西方國家的報告中,每年的發生率約佔全部林巴瘤的1%到10%。柏奇特氏淋巴瘤好發的地區集中在非洲,發生率約是西方國家的20至40倍。根據世界衛生組織的分類,柏奇特氏淋巴瘤組織形態的特徵,除了典型的分類外,還可區分出兩種變異的林巴瘤:非典型柏奇特氏淋巴瘤/類柏奇特氏淋巴瘤以及具有似漿細胞分化的柏奇特氏淋巴瘤。本文中,我們將報告一例發生在成人口腔中的罕見非典型柏奇特氏淋巴瘤/類柏奇特氏淋巴瘤病例,其臨床的特徵近似多發性化膿性肉芽腫。我們也將進一步討論柏奇特氏淋巴瘤與非典型柏奇特氏淋巴瘤/類柏奇特氏淋巴瘤之間的鑑別診斷,以及兩者在組織形態、基因特徵與臨床特徵的異同。

並列摘要


Burkitt's lymphoma (BL) is a high-grade non-Hodgkin's lymphoma (NHL) of B-cell origin. The annual incidence of Burkitt's lymphoma (BL) is low. In western countries, the incidence is 1% to 10% of all lymphoma. The incidence in Africa is 20 to 40 times the incidence of wersten countries. According to the World Health Organization (WI-b) recent classification, Burkitt's lymphoma (BL) depending on its histomorphology is subdivided into classical BL, which includes 2 variants, the atypical Burkitt/Burkitt-like lymphoma (BLL) variant and Burkitt's lymphoma (BL) with plasmacytoid differentiation. In this article, we report an unusual case of adult atypical Burkitt/Burkitt-like lymphoma (BLL) presenting as multiple pyogenic granulomas in oral cavity and review the literature. Further discussion on the differential diagnosis of Burkitt's lymphoma (BL) and atypical Burkitt/Burkitt-like lymphoma (BLL), as well as its histologic features, genetic features and clinical features were presented.

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