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隐匿于成熟浆细胞样树突状细胞增殖中的T淋巴母细胞淋巴瘤:一例报告及文献复习

T Lymphoblastic Lymphoma Hiding in Mature Plasmacytoid Dendritic Cell Proliferation: A Case Report and Literature Review.

作者信息

Deng Cong, Gao Beibei, Wang Tianli, Chang Xiaona, Xiao Guixiang, Xia Qin, Pan Huaxiong, Nie Xiu

机构信息

Department of Pathology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan 430022, China.

出版信息

Diagnostics (Basel). 2023 Oct 19;13(20):3248. doi: 10.3390/diagnostics13203248.

Abstract

To the best of the author's knowledge, studies of mature plasmacytoid dendritic cell proliferation associated with T lymphoblastic lymphoma were extremely rare in the literature. Here, we report a patient who underwent both mature plasmacytoid dendritic cell proliferation and T lymphoblastic lymphoma. With the findings of lymph node biopsy taken from the right cervical and inguinal regions, we identified eye-catching mature plasmacytoid dendritic cells that were considered to be responsible for this lesion at the beginning, until the immunostaining of Ki67 and TDT showed a small group of positive cells hiding in these plasmacytoid dendritic cells. A bone marrow biopsy was also performed on this patient. Microscopically, the hematopoietic tissue was almost completely replaced by lymphoblastoid cells with condensed chromatin, inconspicuous nucleoli and scanty cytoplasm, which were basically the same as those seen in the lymph nodes in morphology. However, there was no sign of plasmacytoid dendritic cells or Langerhans cells in the bone marrow biopsy. With the help of bone marrow biopsy, our final diagnosis of the lymph node was T lymphoblastic lymphoma coexisting with mature plasmacytoid dendritic cell proliferation. Although accumulations of plasmacytoid dendritic cells may occur in some infections or reactive lymphadenopathy, the presence of extensive nodules or infiltration of plasmacytoid dendritic cells strongly reminds the pathologist to carefully evaluate the bone marrow or peripheral blood status of the patient to exclude a hidden myeloid or other neoplasm.

摘要

据作者所知,文献中关于成熟浆细胞样树突状细胞增殖与T淋巴母细胞淋巴瘤相关的研究极为罕见。在此,我们报告一例同时发生成熟浆细胞样树突状细胞增殖和T淋巴母细胞淋巴瘤的患者。通过对右侧颈部和腹股沟区淋巴结活检的结果,我们最初发现了引人注目的成熟浆细胞样树突状细胞,认为其是该病变的病因,直到Ki67和末端脱氧核苷酸转移酶(TDT)免疫染色显示一小群阳性细胞隐藏在这些浆细胞样树突状细胞中。我们还对该患者进行了骨髓活检。显微镜下,造血组织几乎完全被淋巴母细胞样细胞取代,这些细胞染色质浓缩、核仁不明显且细胞质稀少,其形态与淋巴结中的细胞基本相同。然而,骨髓活检中未发现浆细胞样树突状细胞或朗格汉斯细胞的迹象。借助骨髓活检,我们对该淋巴结的最终诊断为T淋巴母细胞淋巴瘤合并成熟浆细胞样树突状细胞增殖。尽管浆细胞样树突状细胞的积聚可能发生在某些感染或反应性淋巴结病中,但浆细胞样树突状细胞广泛结节或浸润的存在强烈提醒病理学家仔细评估患者的骨髓或外周血状况,以排除隐匿性髓系或其他肿瘤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2bc0/10605829/42980768bf22/diagnostics-13-03248-g001.jpg

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