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用于罗萨伊-多夫曼病心脏并发症的腔房旁路手术

Cavoatrial Bypass for Cardiac Complications From Rosai-Dorfman Disease.

作者信息

Nguyen Quynh, Bourke Rachel, Gilbert Richard W, Oldani Graziano, Kim Jong Moo, Lytle Andrew, Cook Richard C, Grocott Hilary P, Price Joel

机构信息

Division of Cardiac Surgery, University of British Columbia, Vancouver, British Columbia, Canada.

Department of Anesthesiology, Pharmacology & Therapeutics, University of British Columbia, Vancouver, British Columbia, Canada.

出版信息

Ann Thorac Surg Short Rep. 2024 Mar 29;2(3):544-547. doi: 10.1016/j.atssr.2024.03.003. eCollection 2024 Sep.

DOI:10.1016/j.atssr.2024.03.003
PMID:39790436
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11708343/
Abstract

Rosai-Dorfman disease (RDD) is a nonmalignant disease of histiocyte proliferation. RDD usually presents with painless cervical lymphadenopathy, although extranodal involvement can occur. Cardiac involvement was reported in <0.1% of cases. We present a case of cardiac RDD with obstruction at the inferior vena cava-right atrial junction.

摘要

罗萨伊-多夫曼病（RDD）是一种组织细胞增殖性非恶性疾病。RDD通常表现为无痛性颈部淋巴结病，不过也可能出现结外受累情况。据报道，心脏受累的病例不到0.1%。我们报告一例发生于下腔静脉-右心房交界处并伴有梗阻的心脏RDD病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/eaf1626125fa/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/c09fcc48c156/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/261c0dce3765/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/eaf1626125fa/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/c09fcc48c156/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/261c0dce3765/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b3e1/11708343/eaf1626125fa/gr3.jpg

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本文引用的文献

1
Case report: Right atrium-inferior vena cava bypass in a patient with unusual cardiac cystic echinococcosis.病例报告：一名患有罕见心脏囊性棘球蚴病患者的右心房-下腔静脉搭桥术
Front Cardiovasc Med. 2022 Nov 3;9:1001073. doi: 10.3389/fcvm.2022.1001073. eCollection 2022.
2
Extranodal Rosai-Dorfman disease arising in the heart: clinical course and review of literature.心脏原发的结外罗道尔夫-多夫曼病：临床经过和文献复习。
Cardiovasc Pathol. 2017 Nov-Dec;31:1-4. doi: 10.1016/j.carpath.2017.06.010. Epub 2017 Jul 4.
3
Mutations in SLC29A3, encoding an equilibrative nucleoside transporter ENT3, cause a familial histiocytosis syndrome (Faisalabad histiocytosis) and familial Rosai-Dorfman disease.
SLC29A3 基因突变导致家族性组织细胞增多症（费萨拉巴德组织细胞增多症）和家族性 Rosai-Dorfman 病，该基因编码一种平衡核苷转运蛋白 ENT3。
PLoS Genet. 2010 Feb 5;6(2):e1000833. doi: 10.1371/journal.pgen.1000833.
4
Sinus histiocytosis with massive lymphadenopathy. A newly recognized benign clinicopathological entity.伴有巨大淋巴结病的窦性组织细胞增多症。一种新认识的良性临床病理实体。
Arch Pathol. 1969 Jan;87(1):63-70.
5
Detection of human herpesvirus 6 in tissues involved by sinus histiocytosis with massive lymphadenopathy (Rosai-Dorfman disease).在伴有巨大淋巴结病的窦性组织细胞增生症（罗萨伊-多夫曼病）累及的组织中检测人疱疹病毒6 。
J Infect Dis. 1992 Aug;166(2):291-5. doi: 10.1093/infdis/166.2.291.