Anaplastic large cell lymphoma presenting as a mass in the uterine cervix: a case report

Pub Date : 2023-11-29 DOI:10.1007/s12308-023-00568-1
Phillip Mingola, Ahmad Alshomrani, Timothy Greiner
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Abstract

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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间变性大细胞淋巴瘤在子宫颈表现为肿块1例
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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