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木村病在一名年轻中东患者中表现为双侧腮腺同时肿胀。

Kimura disease manifesting as synchronous bilateral parotid swelling in a young middle-eastern patient.

作者信息

Faras Fatemah, Abo-Alhassan Fawaz, Al-Sebeih Khalid, Bastaki Jassem

机构信息

Department of ENT, Sabah and Zain Hospital, Ministry of Health, 40188 Mishref, Kuwait.

Department of Surgery, Al-Adan Hospital, Ministry of Health, 40188 Mishref, Kuwait.

出版信息

Case Rep Surg. 2014;2014:648607. doi: 10.1155/2014/648607. Epub 2014 Nov 24.

DOI:10.1155/2014/648607
PMID:25544928
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4259141/
Abstract

Kimura disease is a rare, benign, chronic inflammatory swelling of the subcutaneous tissue, lymph nodes, and glandular tissue. Characteristic features of the disease include, but not limited to, painless subcutaneous head and neck swelling, blood and tissue eosinophilia, and markedly elevated immunoglobulin E (IgE) levels. Herein, we report a rare case of Kimura disease manifesting as synchronous bilateral parotid swelling of 12 years duration in a 33-year-old Middle-Eastern man. To our knowledge only few cases have been reported in the literature involving bilateral parotid glands, and this is the first case to be reported in the Middle East.

摘要

木村病是一种罕见的、良性的、慢性炎症性疾病,可累及皮下组织、淋巴结和腺组织。该疾病的特征包括但不限于无痛性头颈部皮下肿胀、血液和组织嗜酸性粒细胞增多以及免疫球蛋白E(IgE)水平显著升高。在此,我们报告一例罕见的木村病病例,该病例表现为一名33岁中东男性双侧腮腺同步肿胀达12年之久。据我们所知,文献中仅报道了少数累及双侧腮腺的病例,而这是中东地区报道的首例此类病例。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/ddfaf46fc9b0/CRIS2014-648607.007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/729c868003a4/CRIS2014-648607.001.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/729c868003a4/CRIS2014-648607.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/ca276985393a/CRIS2014-648607.002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/e167d046088f/CRIS2014-648607.003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/5c322d14a2d3/CRIS2014-648607.004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/149398a9bc5b/CRIS2014-648607.005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/a1df0f322099/CRIS2014-648607.006.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9f61/4259141/ddfaf46fc9b0/CRIS2014-648607.007.jpg

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Case Rep Surg. 2014;2014:648607. doi: 10.1155/2014/648607. Epub 2014 Nov 24.
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引用本文的文献

1
Stubborn Swellings: A Rare Case of Kimura's Disease Presenting as Parotid Swellings.顽固性肿胀:一例表现为腮腺肿胀的木村病罕见病例。
Cureus. 2024 May 3;16(5):e59570. doi: 10.7759/cureus.59570. eCollection 2024 May.
2
Kimura's Disease: A Rare Cause of Unilateral Tonsillar Enlargement.木村病:单侧扁桃体肿大的罕见病因。
Case Rep Otolaryngol. 2021 Jan 7;2021:8815317. doi: 10.1155/2021/8815317. eCollection 2021.
3
A Rare Case of Kimura Disease with Bilateral Parotid Involvement.双侧腮腺受累的木村病罕见病例。

本文引用的文献

1
Kimura's Disease: A Case Report.木村病:一例报告
Indian J Surg. 2013 Jun;75(Suppl 1):430-1. doi: 10.1007/s12262-012-0750-y. Epub 2012 Oct 2.
2
Kimura's disease: an unusual case of neck mass.木村病:一例罕见的颈部肿块病例。
Indian J Otolaryngol Head Neck Surg. 2008 Dec;60(4):353-5. doi: 10.1007/s12070-008-0101-2. Epub 2008 Nov 7.
3
Magnetic resonance imaging findings in Kimura's disease.木村病的磁共振成像表现
Arch Plast Surg. 2017 Sep;44(5):439-443. doi: 10.5999/aps.2017.44.5.439. Epub 2017 Sep 15.
4
Synchronous Kimura lesions at two different sites-a diagnostic dilemma!两个不同部位的同步木村病变——诊断难题!
Quant Imaging Med Surg. 2016 Apr;6(2):214-7. doi: 10.21037/qims.2015.08.04.
Neuroradiology. 2004 Oct;46(10):855-8. doi: 10.1007/s00234-004-1248-5.
4
Kimura's disease presenting as bilateral parotid masses.木村病表现为双侧腮腺肿块。
Eur Arch Otorhinolaryngol. 2005 Jan;262(1):8-10. doi: 10.1007/s00405-003-0677-9. Epub 2004 Mar 11.
5
Kimura disease: 2 case reports and a literature review.木村病:2例病例报告及文献综述
Cutis. 2002 Jul;70(1):57-61.
6
Angiolymphoid hyperplasia with eosinophilia should not be confused with Kimura's disease.伴嗜酸性粒细胞增多性血管淋巴样增生不应与木村病相混淆。
Acta Ophthalmol Scand. 2001 Feb;79(1):91-3. doi: 10.1034/j.1600-0420.2001.079001091.x.
7
Nephrotic syndrome associated with Kimura disease.与木村病相关的肾病综合征。
Pediatr Nephrol. 2000 Jun;14(6):486-8. doi: 10.1007/s004670050799.
8
Kimura's disease: two case reports and a literature review.木村病:两例病例报告及文献综述
Ann Otol Rhinol Laryngol. 1998 Dec;107(12):1066-71. doi: 10.1177/000348949810701212.
9
[Kimura's disease (eosinophilic lymphfolliculoid granuloma)].[木村病(嗜酸性淋巴滤泡样肉芽肿)]
Nihon Rinsho. 1993 Mar;51(3):785-8.
10
Relative contributions of human types 1 and 2 T-helper cell-derived eosinophilotrophic cytokines to development of eosinophilia.人类1型和2型辅助性T细胞衍生的嗜酸性粒细胞营养因子细胞因子对嗜酸性粒细胞增多症发展的相对贡献。
Blood. 1993 Sep 1;82(5):1471-9.