妊娠期罗赛-多夫曼病罕见病例报告1例

Selvi Kalaivani, N. Siddaraju
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摘要

Rosai-Dorfman病(RDD)也被称为窦性组织细胞增生伴大量淋巴结病,是一种罕见的组织细胞疾病,其组织学特征是细胞内吞噬淋巴细胞。它可能发生在任何年龄组,但最常见于儿童和年轻人。它的特点是无痛,双侧大量颈部淋巴结病。在大约三分之一的患者中,它可以发生在结外的各种部位,在那里它可以有丰富的浆细胞和硬化。我们报告一例罕见的RDD病例,孕妇表现为单侧颈部淋巴结,RDD的特征表现为浆细胞增加和结外部位的硬化。
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Rosai-dorfman disease in pregnancy with rare presentations – A case report
Rosai-Dorfman disease (RDD) also known as sinus histiocytosis with massive lymphadenopathy is a rare disorder of histiocytes characterized histologically by intracellular engulfment of lymphocytes. It may occur in any age group, but is most commonly seen in children and young adults. It is characterized by painless, bilateral massive cervical lymphadenopathy. In approximately one-third of patients it can occur in a variety of extranodal sites where it can have abundant plasma cells and sclerosis. We present a rare case of RDD in a pregnant women who presented with unilateral cervical lymph node with features of RDD showing increase in plasma cells and sclerosis as seen in extranodal sites.
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