起源于中枢神经系统的原发性间变性大细胞淋巴瘤

IF 0.6 4区 医学 Q4 HEMATOLOGY Journal of Hematopathology Pub Date : 2023-12-02 DOI:10.1007/s12308-023-00570-7
Sirichai Puttirangsan, Narittee Sukswai, Sunisa Kongkiatkamon
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引用次数: 0

摘要

一个22岁的男性在急诊科表现进行性头痛,呕吐和水平复视超过2个月的时间。他的左眼视力也变得模糊。在过去的两个月里,他抱怨没有食欲,体重减轻了5公斤。到达后检查发现乳头水肿和双侧外展神经麻痹。运动和感觉功能完好。脑磁共振成像(MRI)示多发轴外结节强化病灶,大小5-10 mm,主要位于大脑两侧镰状区及血管源性脑水肿(图1)。行立体定向脑活检以获得组织诊断。组织学检查显示少量非典型细胞浸润于大量混杂的炎性细胞群中,包括淋巴细胞和组织细胞。非典型细胞为马蹄形核的大细胞(红箭头;图2A ×100和图2B ×400)。免疫组织化学显示强烈、均匀的CD30表达(图2C ×400)和细胞质ALK染色(图2D ×400),以及CD3(图2E ×400)和CD68(图2F ×400)。b细胞标志物(CD20)为阴性(图2G ×400)。
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Primary anaplastic large cell lymphoma arising from central nervous system

A 22-year-old man presented at the emergency department with progressive headache, vomiting and horizontal diplopia over 2-month period. He also developed blurred vision in his left eye. He complained of loss of appetite for the past 2 months, resulting in a 5-kg weight loss. Examination upon arrival revealed papilledema and bilateral abducens nerve palsy. Motor and sensory functions were intact. Magnetic resonance imaging (MRI) of the brain revealed multiple extra-axial nodular enhancing lesions with size of 5–10 mm mainly along with both sides of falx cerebri and vasogenic brain oedema (Fig. 1). Stereotactic brain biopsy was performed to obtain tissue diagnosis. Histologic examination revealed brain infiltration by few atypical cells hidden amongst abundant and mixed population of inflammatory cells including lymphocytes and histiocytes. The atypical cells are large cells with horseshoe nuclei (red arrow; Fig. 2A ×100 and Fig. 2B ×400). Immunohistochemistry showed strong, uniform CD30 expression (Fig. 2C ×400) and cytoplasmic ALK staining (Fig. 2D ×400), as well as for CD3 (Fig. 2E ×400) and CD68 (Fig. 2F ×400). B-cell markers (CD20) were negative (Fig. 2G ×400).

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来源期刊
Journal of Hematopathology
Journal of Hematopathology HEMATOLOGYPATHOLOGY-PATHOLOGY
CiteScore
0.80
自引率
0.00%
发文量
45
期刊介绍: The Journal of Hematopathology aims at providing pathologists with a special interest in hematopathology with all the information needed to perform modern pathology in evaluating lymphoid tissues and bone marrow. To this end the journal publishes reviews, editorials, comments, original papers, guidelines and protocols, papers on ancillary techniques, and occasional case reports in the fields of the pathology, molecular biology, and clinical features of diseases of the hematopoietic system. The journal is the unique reference point for all pathologists with an interest in hematopathology. Molecular biologists involved in the expanding field of molecular diagnostics and research on lymphomas and leukemia benefit from the journal, too. Furthermore, the journal is of major interest for hematologists dealing with patients suffering from lymphomas, leukemias, and other diseases. The journal is unique in its true international character. Especially in the field of hematopathology it is clear that there are huge geographical variations in incidence of diseases. This is not only locally relevant, but due to globalization, relevant for all those involved in the management of patients.
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