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Primary malignant lymphoma combined with clinically silent pheochromocytoma in the same adrenal gland

机译:原发性恶性淋巴瘤合并同一肾上腺的临床沉默嗜铬细胞瘤

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摘要

An increased number of adrenal tumors are now diagnosed due to the increased number of abdominal CT scans being performed. We present the first case of malignant lymphoma combined with clinically “silent” pheochromocytoma in the same adrenal gland. An abdominal CT scan demonstrates unilateral adrenal lesion which suggests pheochromocytoma or adrenal carcinoma. Laboratory examinations revealed a slight increase of 24-h urine vanillylmandelic acid and 24-h urinary methanephrine excretion. Histological examination revealed two intermingled tumor cell proliferations—diffuse B cell lymphoma and pheochromocytoma.Unexpected coexistence of catecholamine-producing tumor with the other adrenal lesion can lead to serious complications of diagnosis and treatment. The adequate preparation for surgery can protect patient from threatening catecholamine crisis.
机译:由于执行的腹部CT扫描数量增加,现在诊断出肾上腺肿瘤的数量增加。我们介绍了在同一肾上腺中合并临床上“沉默的”嗜铬细胞瘤的首例恶性淋巴瘤。腹部CT扫描显示单侧肾上腺病变,提示嗜铬细胞瘤或肾上腺癌。实验室检查发现24小时尿液香草去氧扁桃酸和24小时尿液甲基苯丙氨酸排泄量略有增加。组织学检查显示,两种肿瘤细胞相互扩散,即弥漫性B细胞淋巴瘤和嗜铬细胞瘤。产生儿茶酚胺的肿瘤与其他肾上腺病变的意外并存会导致严重的诊断和治疗并发症。充分的手术准备可以保护患者免受威胁儿茶酚胺的威胁。

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