Castleman病1例报告

S. Jha, A. Jha, D. Regmi, U. Bhatta, Goody Jha
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引用次数: 0

摘要

Castleman病(CD)是一组具有共同淋巴结组织学特征的淋巴增生性疾病。它可以是单中心的,也可以是多中心的。单中心Castleman病(UCD)是局部的,预后良好,而多中心Castleman病(MCD)是一种全身性疾病,最常见于HIV感染,与人类疱疹病毒相关。腹部和骨盆的Castleman病罕见,易误诊,但其特有的影像学特征有助于诊断和鉴别诊断。单中心Castleman病(UCD)是罕见的,没有可靠的估计其在人群中的发病率。虽然UCD可以发生在任何年龄,但它通常是年轻人的疾病。发病时的中位年龄约为35岁。3、4
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Castleman Disease: A case report
Castleman disease (CD) is a group of lymphoproliferative disorders with common lymph node histological features. It may be either unicentric or multicentric. Unicentric Castleman disease (UCD) is localized and carries an excellent prognosis, whereas multicentric Castleman disease (MCD) is a systemic disease occurring most commonly in the setting of HIV infection and is associated with human herpesvirus 8.1Castleman disease in the abdomen and pelvis is rare and liable to misdiagnosis, but its characteristic imaging features can help in the diagnosis and differential diagnosis.2Unicentric Castleman disease (UCD) is rare, and there are no reliable estimates of its incidence in the population. While UCD can occur at any age, it is generally a disease of younger adults. The median age at presentation is approximately 35 years.3, 4
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