窦性组织细胞增多症伴大量淋巴结病变,(Rosai-Dorfman病)伴胆汁淤积性黄疸

K. Mpho, Elnagar Ali Ahmed, Mashoshoe Kgataki Sam, T. Preetha, Ngwata Portia, Bida Mishack
{"title":"窦性组织细胞增多症伴大量淋巴结病变,(Rosai-Dorfman病)伴胆汁淤积性黄疸","authors":"K. Mpho, Elnagar Ali Ahmed, Mashoshoe Kgataki Sam, T. Preetha, Ngwata Portia, Bida Mishack","doi":"10.21767/amj.2018.3456","DOIUrl":null,"url":null,"abstract":"Introduction Sinus histiocytosis with massive lymphadenopathy is a rare histiocytic disease first described by Rosai and Dorfman in 1969. The typical presentation is that of cervical and often widespread painless lymphadenopathy. Case report We present a 33-year-old gentleman, with one-month history of pruritus, abdominal pain, jaundice and dark urine, jaundice, scratch marks, large inguinal lymph nodes, an enlarged liver and spleen. CT scan confirmed ultrasound findings and suggested that splenic lesions were microabscesses. Biopsy of the lymph nodes revealed features in keeping with sinus histiocytosis with dermatophatic lymphadenopathy. Discussion This is our second case of sinus histiocytosis in two years.","PeriodicalId":46823,"journal":{"name":"Australasian Medical Journal","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2018-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Sinus histiocytosis with massive lymphadenopathy, (Rosai-Dorfman Disease) with cholastatic jaundice in an HIV positive patient\",\"authors\":\"K. Mpho, Elnagar Ali Ahmed, Mashoshoe Kgataki Sam, T. Preetha, Ngwata Portia, Bida Mishack\",\"doi\":\"10.21767/amj.2018.3456\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Introduction Sinus histiocytosis with massive lymphadenopathy is a rare histiocytic disease first described by Rosai and Dorfman in 1969. The typical presentation is that of cervical and often widespread painless lymphadenopathy. Case report We present a 33-year-old gentleman, with one-month history of pruritus, abdominal pain, jaundice and dark urine, jaundice, scratch marks, large inguinal lymph nodes, an enlarged liver and spleen. CT scan confirmed ultrasound findings and suggested that splenic lesions were microabscesses. Biopsy of the lymph nodes revealed features in keeping with sinus histiocytosis with dermatophatic lymphadenopathy. Discussion This is our second case of sinus histiocytosis in two years.\",\"PeriodicalId\":46823,\"journal\":{\"name\":\"Australasian Medical Journal\",\"volume\":\"11 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2018-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Australasian Medical Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.21767/amj.2018.3456\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Australasian Medical Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21767/amj.2018.3456","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

摘要

窦性组织细胞增多症合并大量淋巴结病是一种罕见的组织细胞疾病,由Rosai和Dorfman于1969年首次报道。典型的表现是颈部无痛性淋巴结病,通常分布广泛。我们报告一位33岁的男性患者,有瘙痒、腹痛、黄疸及尿色深、黄疸、抓痕、腹股沟淋巴结大、肝脾肿大等病史一个月。CT扫描证实超声表现,提示脾病变为微脓肿。淋巴结活检显示的特征与皮肤淋巴病变的窦性组织细胞增多症一致。这是我们两年内第二例窦性组织细胞增多症。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
Sinus histiocytosis with massive lymphadenopathy, (Rosai-Dorfman Disease) with cholastatic jaundice in an HIV positive patient
Introduction Sinus histiocytosis with massive lymphadenopathy is a rare histiocytic disease first described by Rosai and Dorfman in 1969. The typical presentation is that of cervical and often widespread painless lymphadenopathy. Case report We present a 33-year-old gentleman, with one-month history of pruritus, abdominal pain, jaundice and dark urine, jaundice, scratch marks, large inguinal lymph nodes, an enlarged liver and spleen. CT scan confirmed ultrasound findings and suggested that splenic lesions were microabscesses. Biopsy of the lymph nodes revealed features in keeping with sinus histiocytosis with dermatophatic lymphadenopathy. Discussion This is our second case of sinus histiocytosis in two years.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Australasian Medical Journal
Australasian Medical Journal MEDICINE, GENERAL & INTERNAL-
自引率
0.00%
发文量
0
期刊最新文献
Vitamin D supplementation as a fall prevention method: A systematic review Epidemiological study of scarlet fever in Shenyang City, China Local anti-inflammatory effect of vitamin D in acute and chronic gouty arthritis Differentiation of N-acetyltransferase 2 (NAT2) rapid and intermediate acetylator based on genotype and urinary assay Are we facing NOVICHOK nerve agent threat?
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1