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白塞病在一名患菊池-藤本病患者中表现为全结肠溃疡:一种罕见的胃肠道表现。

Behcet's Disease Presenting as Pancolonic Ulcerations in a Patient With Kikuchi-Fujimoto Disease: A Rare Gastrointestinal Manifestation.

作者信息

Lin Frank, Obeid Ayah, Bhalala Harsh, Patel Nishit, Ge Li, Modi Ronak

机构信息

Internal Medicine, St. Luke's University Health Network, Bethlehem, PA.

出版信息

ACG Case Rep J. 2024 Aug 30;11(9):e01455. doi: 10.14309/crj.0000000000001455. eCollection 2024 Sep.

DOI:10.14309/crj.0000000000001455
PMID:39221232
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11365614/
Abstract

Kikuchi-Fujimoto disease (KFD) is a rare and self-limiting disorder characterized by cervical lymphadenopathy and fever. In this report, we present a case of a 24-year-old man with known history of KFD who presented with lower gastrointestinal bleeding and acute blood loss anemia. Further evaluation with colonoscopy showed widespread ulcerations in the colon and terminal ileum with suspicion for Behcet's disease. Biopsy from the colonic mucosa and ileocecal valve demonstrated focal ulcer with cryptitis and lymphoid aggregates that can be seen in Behcet's syndrome; however, it lacks specificity and Behcet's disease is a clinical diagnosis. This case emphasizes the importance of including gastrointestinal bleeding as a potential manifestation due to Behcet's disease in patients diagnosed with KFD.

摘要

菊池-藤本病(KFD)是一种罕见的自限性疾病,其特征为颈部淋巴结病和发热。在本报告中,我们呈现了一例24岁男性病例,该患者有菊池-藤本病病史,此次出现下消化道出血和急性失血性贫血。结肠镜进一步检查显示结肠和回肠末端广泛溃疡,怀疑为白塞病。结肠黏膜和回盲瓣活检显示局灶性溃疡伴隐窝炎和淋巴样聚集,这在白塞综合征中可见;然而,其缺乏特异性,白塞病是一种临床诊断。该病例强调了在诊断为菊池-藤本病的患者中,将胃肠道出血作为白塞病潜在表现之一的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b735/11365614/3aeb1a175ceb/ac9-11-e01455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b735/11365614/54f544178e67/ac9-11-e01455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b735/11365614/3aeb1a175ceb/ac9-11-e01455-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b735/11365614/54f544178e67/ac9-11-e01455-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/b735/11365614/3aeb1a175ceb/ac9-11-e01455-g002.jpg

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Behcet's Disease Presenting as Pancolonic Ulcerations in a Patient With Kikuchi-Fujimoto Disease: A Rare Gastrointestinal Manifestation.白塞病在一名患菊池-藤本病患者中表现为全结肠溃疡:一种罕见的胃肠道表现。
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本文引用的文献

1
Kikuchi Disease After SARS-CoV-2 Vaccination: A Case Report With Immunohistochemical Analyses.接种 SARS-CoV-2 疫苗后的菊池病:一例病例报告并免疫组化分析。
Int J Surg Pathol. 2024 Sep;32(6):1123-1128. doi: 10.1177/10668969231212428. Epub 2023 Nov 19.
2
Kikuchi-Fujimoto Disease Following COVID-19 Vaccination: Experience at a Population-Based Referral Center.接种 COVID-19 疫苗后的菊池-藤本病:基于人群的转诊中心的经验。
Am J Clin Pathol. 2023 Aug 1;160(2):114-118. doi: 10.1093/ajcp/aqad032.
3
Kikuchi-Fujimoto Disease: A Case of SARS-CoV-2 Infection Triggering the Rare Disease.
菊池-藤本病:1例由新型冠状病毒感染引发的罕见疾病
Cureus. 2023 Mar 7;15(3):e35858. doi: 10.7759/cureus.35858. eCollection 2023 Mar.
4
Kikuchi's Disease Diagnosed by an Excisional Biopsy in a Patient With COVID-19.通过切除活检诊断为菊池病的1例新冠肺炎患者
Cureus. 2023 Feb 21;15(2):e35251. doi: 10.7759/cureus.35251. eCollection 2023 Feb.
5
Are the specific and nonspecific ANA staining patterns of Behçet's Disease patients important?贝切特病患者的特异性和非特异性抗核抗体染色模式重要吗?
Reumatol Clin (Engl Ed). 2022 Mar;18(3):147-149. doi: 10.1016/j.reumae.2020.11.005.
6
Histiocytic Necrotizing Lymphadenitis Mimicking Acute Appendicitis in a Child: A Case Report.儿童组织细胞性坏死性淋巴结炎酷似急性阑尾炎:一例报告
Front Pediatr. 2021 Sep 17;9:682738. doi: 10.3389/fped.2021.682738. eCollection 2021.
7
Kikuchi-Fujimoto disease associated with neuro-Behçet's disease.
Clin Neurol Neurosurg. 2021 Mar;202:106541. doi: 10.1016/j.clineuro.2021.106541. Epub 2021 Feb 2.
8
Kikuchi-Fujimoto Disease Associated with Sjögren's Syndrome: A Case Report.与干燥综合征相关的菊池-藤本病:一例报告
Eur J Case Rep Intern Med. 2018 May 25;5(5):000856. doi: 10.12890/2018_000856. eCollection 2018.
9
Take a second look: it's Kikuchi's disease! A case report and review of literature.再看一眼:这是菊池病!一例病例报告及文献复习。
Clin Pract. 2018 Dec 12;8(4):1095. doi: 10.4081/cp.2018.1095. eCollection 2018 Oct 26.
10
Kikuchi-Fujimoto Disease: A Review.菊池-藤本病:综述。
Arch Pathol Lab Med. 2018 Nov;142(11):1341-1346. doi: 10.5858/arpa.2018-0219-RA.