Rare Case of Primary Adenoid Cystic Carcinoma of the Lung With Bilateral Kidney and Liver Metastasis.

Talwinder Nagi, Rannah Dabiri, Yousra Gheit, Abanoub Zaki, Willy Gan, Alberto Torres, Touqir Zahra, Sachin Sule
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引用次数: 1

Abstract

Adenoid cystic carcinoma (ACC) is a rare epithelial tumor that is found in the salivary glands. It is typically slow-growing and follows an indolent course. While it can hematogenously spread to the lungs, distant metastases are rarely reported. Primary ACC in the lung is not common and makes up only 0.04-0.2% of all primary lung tumors. In addition, metastasis of the ACC to liver and bilateral kidneys is not common frequently documented. In this case report, we present a patient with unusual metastases of ACC, as well as non-specific symptoms that warrant discussion for ACC as potential differentials in the appropriate clinical setting.

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原发性肺腺样囊性癌合并双侧肾脏及肝脏转移的罕见病例。
腺样囊性癌(ACC)是一种罕见的涎腺上皮性肿瘤。它通常生长缓慢,并遵循一种惰性过程。虽然它可以通过血液扩散到肺部,但很少有远处转移的报道。原发性ACC在肺部并不常见,仅占所有原发性肺肿瘤的0.04-0.2%。此外,ACC转移到肝脏和双侧肾脏并不常见。在这个病例报告中,我们提出了一个不寻常的ACC转移患者,以及非特异性症状,需要在适当的临床环境中讨论ACC的潜在差异。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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