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首页> 外文期刊>American Journal of Dermatopathology >Hyaline-vascular castleman disease: A rare cause of solitary subcutaneous soft tissue mass
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Hyaline-vascular castleman disease: A rare cause of solitary subcutaneous soft tissue mass

机译:透明血管恶性肿瘤:孤立性皮下软组织肿块的罕见原因

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摘要

Castleman disease (CD) is a rare lymphoproliferative disorder that primarily affects mediastinal, retroperitoneal, and cervical lymph nodes. Clinically, these lesions occur as a localized (unicentric) or less frequently as a systemic (multicentric) disease. Two main distinct histologic variants are recognized, the more common hyaline-vascular (HV) type and the plasma cell (PC) type. Extranodal Castleman disease, HV type (HVCD) is even less common. We describe a case of subcutaneous HVCD in a 57-year-old woman with a palpable chest mass and without systemic symptoms. Although the histologic findings are similar to those of HVCD in lymph nodes and other sites, a plethora of differential diagnosis is raised particularly with the more commonly occurring lymphoproliferative lesions in this location. This is one of the few bona fide cases of HVCD in subcutaneous location published to date. A review of the literature with an emphasis on pathogenesis of the disease subtypes is presented.
机译:Castleman病(CD)是一种罕见的淋巴增生性疾病,主要影响纵隔,腹膜后和颈淋巴结。临床上,这些病变以局限性(单中心)发生或以全身性(多中心)疾病发生的频率更低。认识到两种主要的不同组织学变异,更常见的透明血管(HV)型和浆细胞(PC)型。结外Castleman病,HV型(HVCD)更为罕见。我们描述了一名57岁的女性,有明显的胸部肿块且没有全身症状的皮下HVCD病例。尽管在淋巴结和其他部位的组织学发现与HVCD相似,但是特别是在该部位更常见的淋巴增生性病变中,引起了许多鉴别诊断。这是迄今为止在皮下定位的少数几个真正的HVCD病例之一。提出了对疾病亚型发病机理的文献综述。

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