间变性大细胞淋巴瘤在子宫颈表现为肿块1例

IF 0.6 4区 医学 Q4 HEMATOLOGY Journal of Hematopathology Pub Date : 2023-11-29 DOI:10.1007/s12308-023-00568-1
Phillip Mingola, Ahmad Alshomrani, Timothy Greiner
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引用次数: 0

摘要

t细胞淋巴瘤是一种极其罕见的恶性肿瘤在女性生殖道。大多数报告的淋巴瘤病例为b细胞淋巴瘤。一些原发t细胞淋巴瘤累及阴道或外阴的病例已被报道。我们报告第一例间变性大细胞淋巴瘤(ALCL)表现为子宫颈肿块。患者为24岁女性,因月经过多、盗汗和体重减轻40磅就诊于急诊室。通过免疫组化检查证实ALCL的诊断,CD30和ALK表达强烈。荧光杂交显示间变性淋巴瘤激酶(ALK)基因重排。由于ALCL可能具有不同的t细胞抗原表达,当CD45和/或CD3为阴性,而筛选上皮染色癌(如p63和EMA)为阳性时,诊断很容易被遗漏。当观察到肾形核时,必须进行CD30检查以提高对ALCL的考虑。
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Anaplastic large cell lymphoma presenting as a mass in the uterine cervix: a case report

T-cell lymphoma is an extremely rare form of malignancy in the female genital tract. Most of the reported cases of lymphoma are B-cell lymphomas. A few cases of primary T-cell lymphomas involving the vagina or the vulva have been reported. We are reporting the first case of anaplastic large cell lymphoma (ALCL) presenting as a uterine cervical mass. The patient is a 24-year-old female who presented to the emergency room with a history of menorrhagia, night sweats and 40-pound weight loss. The diagnosis of ALCL was confirmed through immunohistochemical studies with strong CD30 and ALK expression. Fluorescent hybridization showed a rearrangement of the anaplastic lymphoma kinase (ALK) gene. Since ALCL may have a variable expression of T-cell antigens, the diagnosis may easily be missed when CD45 and/or CD3 is negative, and screening epithelial stains for carcinoma (e.g., p63 and EMA) are positive. CD30 must be performed to raise the consideration of ALCL when reniform nuclei are observed.

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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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