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无粒细胞浸润的坏死性淋巴结炎(菊池病)。

Necrotising lymphadenitis without granulocytic infiltration (Kikuchi's disease).

作者信息

Ali M H, Horton L W

出版信息

J Clin Pathol. 1985 Nov;38(11):1252-7. doi: 10.1136/jcp.38.11.1252.

DOI:10.1136/jcp.38.11.1252
PMID:4066984
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC499422/
Abstract

Kikuchi's disease (necrotising lymphadenitis) is characterised by cervical lymphadenopathy in young patients and may be mistaken for malignant disease both clinically and histologically. Microscopically, there is a varying degree of effacement of the lymph node architecture and necrosis with an infiltrate of "histiocytic" cells and absence of polymorphs. The disease is of unknown aetiology. It was originally described in Japan, and only 27 cases have been reported elsewhere (none in the United Kingdom), although it has probably been seen but not recognised. The clinical, histopathological, electron microscopic, and immunohistological findings in four cases of the disease were evaluated.

摘要

菊池病(坏死性淋巴结炎)的特征是年轻患者出现颈部淋巴结病,在临床和组织学上都可能被误诊为恶性疾病。显微镜下,淋巴结结构有不同程度的破坏,伴有坏死,有“组织细胞”浸润且无多形核细胞。该病病因不明。它最初在日本被描述,其他地方仅报告了27例(英国无病例报告),尽管可能已被发现但未被识别。对该病4例患者的临床、组织病理学、电子显微镜和免疫组织学检查结果进行了评估。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/a078fbf45ba8/jclinpath00194-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/c6de131fd54a/jclinpath00194-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/7ddc91b728a4/jclinpath00194-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/5ba67a5ffb04/jclinpath00194-0053-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/ce02ebe78254/jclinpath00194-0053-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/f2a66fecdc2f/jclinpath00194-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/67fa874cd4f5/jclinpath00194-0054-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/2e24878cb86f/jclinpath00194-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/a078fbf45ba8/jclinpath00194-0056-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/c6de131fd54a/jclinpath00194-0053-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/7ddc91b728a4/jclinpath00194-0053-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/5ba67a5ffb04/jclinpath00194-0053-c.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/ce02ebe78254/jclinpath00194-0053-d.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/f2a66fecdc2f/jclinpath00194-0054-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/67fa874cd4f5/jclinpath00194-0054-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/2e24878cb86f/jclinpath00194-0055-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e99a/499422/a078fbf45ba8/jclinpath00194-0056-a.jpg

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引用本文的文献

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Necrotizing lymphadenitis (NEL) is a systemic disease characterized by blastic transformation of CD8+ cells and apoptosis of CD4+ cells.坏死性淋巴结炎(NEL)是一种全身性疾病,其特征为 CD8+细胞的母细胞转化和 CD4+细胞的凋亡。
Virchows Arch. 2014 Jan;464(1):95-103. doi: 10.1007/s00428-013-1516-z. Epub 2013 Nov 30.
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Necrotizing cervical lymphadenopathy: Kikuchi-Fujimoto disease in a young male.坏死性颈淋巴结病:一名年轻男性的菊池-藤本病
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Kikuchi-Fujimoto disease: a case report.

本文引用的文献

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Histiocytic necrotizing lymphadenitis without granulocytic infiltration.无粒细胞浸润的组织细胞性坏死性淋巴结炎
Virchows Arch A Pathol Anat Histol. 1982;395(3):257-71. doi: 10.1007/BF00429352.
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Erythrophagocytic T gamma lymphoma: a clinicopathologic entity resembling malignant histiocytosis.噬红细胞性Tγ淋巴瘤:一种类似恶性组织细胞增多症的临床病理实体。
N Engl J Med. 1981 Mar 12;304(11):648-53. doi: 10.1056/NEJM198103123041106.
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Necrotizing pseudolymphomatous lymphadenitis and rapidly fatal lymphoma in Okinawa.冲绳的坏死性假淋巴瘤性淋巴结炎及迅速致死性淋巴瘤
菊池-藤本病:一例病例报告。
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Myeloperoxidase expression by histiocytes in Kikuchi's and Kikuchi-like lymphadenopathy.组织细胞在菊池病及类菊池病淋巴结病中的髓过氧化物酶表达
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Analysis of herpesvirus genomes in Kikuchi's disease.菊池病中疱疹病毒基因组的分析。
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Classification of haemolytic uraemic syndrome.溶血性尿毒症综合征的分类。
J Clin Pathol. 1986 Jul;39(7):812-3. doi: 10.1136/jcp.39.7.812-b.
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Necrotising lymphadenitis without granulocytic infiltration (Kikuchi's disease).无粒细胞浸润的坏死性淋巴结炎(菊池病)。
J Clin Pathol. 1986 Jul;39(7):811-2. doi: 10.1136/jcp.39.7.811-c.
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Immunohistological study of histiocytic necrotizing lymphadenitis.
Virchows Arch A Pathol Anat Histopathol. 1986;409(3):299-311. doi: 10.1007/BF00708248.
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Necrotising lymphadenitis without granulocytic infiltration: case from Western Samoa.无粒细胞浸润的坏死性淋巴结炎:来自西萨摩亚的病例
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Necrotizing lymphadenitis: a clinicopathological and immunohistochemical study of four familial cases and five recurrent cases.坏死性淋巴结炎:4例家族性病例和5例复发性病例的临床病理及免疫组化研究
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Immunohistology and aetiology of histiocytic necrotizing lymphadenitis. Report of three instructive cases.组织细胞性坏死性淋巴结炎的免疫组织学与病因学。三例典型病例报告。
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Necrotizing lymphadenitis: possible acute toxoplasmic infection.
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