Castleman病:由于一种罕见的腹内病变

FORBES Pub Date : 2021-01-01 DOI:10.5222/FORBES.2021.66376
M. Karacaoğlu, N. Yurttutan, B. Kizildag, Turgay Kara, S. Koçarslan
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引用次数: 0

摘要

Castleman病(CD)是一种罕见的良性疾病,病因不明。又称血管滤泡性淋巴结增生、巨大淋巴结增生、淋巴结错构瘤、良性巨大淋巴瘤。组织学上分为透明血管型和浆细胞型,但两种类型的特征很少共存。单中心型多为透明血管型,多中心型多为浆细胞型。虽然它通常位于胸腔,但它可以遍布全身。唾液腺、肺、胰腺、喉、腮腺、脑膜,甚至肢体肌肉都可能受到淋巴外扩散的影响。由于它位于胸腔的中纵隔和前纵隔,因此应与纵隔自身免疫性疾病和肿瘤性疾病相鉴别。在这个病例报告中,我们的目的是报告一个罕见的腹腔内病变的CD病例的影像学表现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Castleman’s Disease: Due to a Rare Intraabdominal Location
Castleman disease (CD) is a rare benign disease with unknown etiology. It is also called angiofollicular lymph node hyperplasia, giant lymph node hyperplasia, lymph node hamartoma, benign giant lymphoma. Histologically, it is classified as hyaline vascular and plasma cell variant, but rarely features of two types can coexist. Most of the cases with unisentric disease are hyaline vascular and most of the cases with multicentric disease are in plasma cell histological type. Although it is frequently located in thorax, it can be found throughout the body. Salivary glands, lungs, pancreas, larynx, parotid gland, meninges, and even limb muscles can be affected as extralymphatic spread. Since it is localized in the middle and anterior mediastinum in the thorax, it should be differentiated from mediastinal autoimmune and neoplastic diseases. In this case report, we aimed to present the radiological findings of a CD case with a rare intraabdominal location.
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来源期刊
FORBES
FORBES BUSINESS, FINANCE-
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