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Bilateral primary adrenal diffuse large B cell lymphoma without adrenal insufficiency: A case report and review of the literature

机译:无肾上腺功能不全的双侧原发性肾上腺弥漫性大B细胞淋巴瘤:1例报道并文献复习

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摘要

Primary adrenal lymphoma (PAL) is an infrequent malignant tumor, occurring in the bilateral adrenal glands as a mass in the majority of cases. The current study presents a case of bilateral primary adrenal diffuse large B cell lymphoma in a 52-year-old female patient, who presented with abdominal pain in the left lumbar region for ~2 weeks. Abdominal ultrasound examination and computed tomography scanning revealed a mass of 132×119×101 mm on the left adrenal gland and a mass of 53×27 mm on the right adrenal gland. A percutaneous biopsy was performed and histopathological examination further confirmed this lesion as diffuse large B cell lymphoma. The present study highlights the importance of early diagnosis of PAL, and performs a literature review of the subject.
机译:原发性肾上腺淋巴瘤(PAL)是一种罕见的恶性肿瘤,在大多数情况下在双侧肾上腺以肿块的形式出现。当前的研究显示了一例52岁女性患者的双侧原发性肾上腺弥漫性大B细胞淋巴瘤,该患者在左腰区出现腹痛约2周。腹部超声检查和计算机断层扫描显示,左肾上腺的质量为132×119×101 mm,右肾上腺的质量为53×27 mm。经皮穿刺活检,组织病理学检查进一步证实该病变为弥漫性大B细胞淋巴瘤。本研究强调了PAL早期诊断的重要性,并对该主题进行了文献综述。

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