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病例报告:木村病中罕见的鼻额部肿块病例

Case Report: A Rare Case of Nasal Forehead Mass in Kimura's Disease.

作者信息

Zhao He, Cao Zhi-Wei, Gu Zhao-Wei

机构信息

Department of Otolaryngology Head and Neck Surgery, Shengjing Hospital of China Medical University, Shenyang, China.

出版信息

Front Surg. 2021 May 21;8:672291. doi: 10.3389/fsurg.2021.672291. eCollection 2021.

DOI:10.3389/fsurg.2021.672291
PMID:34095210
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8176203/
Abstract

Kimura's disease is a rheumatic immune disease and head and neck lymph nodes are often involved. A mass occurring in the nasal forehead is rare. Good prognosis after surgical resection by glucocorticoid therapy is more rare. We report the rare case of a nasal forehead mass in a 45-year-old male patient with Kimura's disease. The patient underwent resection of the mass in October 2018 in a local hospital and the postoperative pathology was unclear. He then underwent a second resection in our department in December 2019 mainly because growth of the mass was affecting his appearance. Postoperative pathology confirmed that the patient had Kimura's disease, and he accepted systemic treatment with prednisone. We followed the patient for 10 months after surgery. He is now recovering well and continues to be closely monitored during follow-up. It is rare that the painless mass in the nasal forehead is diagnosed as a Kimura's disease.After completely resection of the mass and systemic treatment with prednisone, the patient had a good outcome. We provide experience for the treatment of Kimura's disease in nasal forehead.

摘要

木村病是一种风湿免疫性疾病,常累及头颈部淋巴结。发生于鼻额部的肿块较为罕见。经糖皮质激素治疗后手术切除预后良好的情况更为罕见。我们报告一例45岁男性木村病患者鼻额部肿块的罕见病例。该患者于2018年10月在当地医院接受了肿块切除术,术后病理结果不明确。2019年12月,他因肿块生长影响外观,在我科接受了二次切除手术。术后病理证实患者患有木村病,随后他接受了泼尼松全身治疗。术后我们对患者进行了10个月的随访。他目前恢复良好,随访期间仍在持续密切监测。鼻额部无痛性肿块被诊断为木村病的情况较为罕见。在肿块完全切除并接受泼尼松全身治疗后,患者预后良好。我们为鼻额部木村病的治疗提供了经验。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/c1fe30828dbd/fsurg-08-672291-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/3918983466f2/fsurg-08-672291-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/9fc71a7c6d0a/fsurg-08-672291-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/c1fe30828dbd/fsurg-08-672291-g0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/3918983466f2/fsurg-08-672291-g0001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/9fc71a7c6d0a/fsurg-08-672291-g0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a42e/8176203/c1fe30828dbd/fsurg-08-672291-g0003.jpg

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本文引用的文献

1
Kimura Disease with Parotid Swelling and Cervical Lymphadenopathy: A Case Report and Literature Review.伴有腮腺肿大和颈部淋巴结病的木村病:一例报告及文献复习
Medeni Med J. 2020;35(2):170-174. doi: 10.5222/MMJ.2020.84594. Epub 2020 Jun 30.
2
Clinical analysis of Kimura's disease in 24 cases from China.24例中国木村病的临床分析
BMC Surg. 2020 Jan 2;20(1):1. doi: 10.1186/s12893-019-0673-7.
3
KIMURA'S Disease - An E[X]clusive Condition.木村病——一种独特的病症。
Ann Maxillofac Surg. 2019 Jan-Jun;9(1):183-187. doi: 10.4103/ams.ams_159_17.
4
Kimura's disease with membranoproliferative glomerulonephritis: a case report with literature review.Kimura 病合并膜增生性肾小球肾炎:病例报告并文献复习。
Ren Fail. 2019 Nov;41(1):126-130. doi: 10.1080/0886022X.2019.1584115.
5
Nephrotic syndrome associated with Kimura's disease: a case report and literature review.Kimura 病相关性肾病综合征:病例报告及文献复习。
BMC Nephrol. 2018 Nov 8;19(1):316. doi: 10.1186/s12882-018-1123-y.
6
Kimura disease.
Dermatol Online J. 2017 Oct 15;23(10):13030/qt4jx9v026.
7
Concurrent eosinophilia and IgG4-related disease in a child: A case report and review of the literature.儿童并发嗜酸性粒细胞增多症与IgG4相关疾病:一例报告及文献复习
Exp Ther Med. 2018 Mar;15(3):2739-2748. doi: 10.3892/etm.2018.5743. Epub 2018 Jan 12.
8
Angiolymphoid hyperplasia with eosinophilia versus Kimura's disease: a case report and a clinical and histopathological comparison.嗜酸性粒细胞增多性血管淋巴样增生与木村病:一例报告及临床与组织病理学比较
An Bras Dermatol. 2017 May-Jun;92(3):392-394. doi: 10.1590/abd1806-4841.20175318.
9
Kimura's Disease without Peripheral Eosinophilia: An Unusual and Challenging Case Simulating Venous Malformation on Imaging Studies-Case Report and Review of literature.无外周嗜酸性粒细胞增多的木村病:1例影像学表现类似静脉畸形的罕见且具有挑战性的病例——病例报告及文献复习
J Clin Diagn Res. 2017 Jun;11(6):ME01-ME04. doi: 10.7860/JCDR/2017/28603.10063. Epub 2017 Jun 1.
10
Angiolymphoid Hyperplasia with Eosinophilia Involving the Occipital Artery: Case Report and Review of Literature.累及枕动脉的嗜酸性粒细胞增多性血管淋巴样增生:病例报告及文献复习
J Clin Diagn Res. 2017 Mar;11(3):ZD21-ZD23. doi: 10.7860/JCDR/2017/23323.9569. Epub 2017 Mar 1.