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狼疮性淋巴结炎:一例经冰冻切片免疫组织学研究的病例报告。

Lupus lymphadenitis: report of a case with immunohistologic studies on frozen sections.

作者信息

Medeiros L J, Kaynor B, Harris N L

机构信息

Department of Pathology, Massachusetts General Hospital, Boston.

出版信息

Hum Pathol. 1989 Mar;20(3):295-9. doi: 10.1016/0046-8177(89)90141-x.

DOI:10.1016/0046-8177(89)90141-x
PMID:2656495
Abstract

A case of lupus lymphadenitis with frozen section immunohistologic studies is presented. Clinically, the patient had well-documented systemic lupus erythematosus (SLE) when rapid development of generalized lymphadenopathy raised the possibility of a diagnosis of malignant lymphoma. Histologically, the findings of paracortical foci of necrosis and hematoxylin bodies were diagnostic of SLE. Granulocytes were absent. Monoclonal antibodies applied to frozen sections demonstrated two predominant cell populations within and surrounding the paracortical zones of necrosis: OKM1+, Leu-M1+ histiocytes and OKT8+, Leu-4+ T cytotoxic/suppressor cells. In the lymph node not involved by necrosis, lymphoid follicles were composed of polytypic B cells and the interfollicular regions of T cells. Leu-3a+, Leu-4+ T helper/inducer cells outnumbered T cytotoxic/suppressor cells in a 3:1 ratio. Since lupus lymphadenitis may closely resemble histiocytic necrotizing lymphadenitis of Kikuchi and Fujimoto, particularly if hematoxylin bodies are not found, we compared the findings in this case with findings of cases of histiocytic necrotizing lymphadenitis of Kikuchi and Fujimoto reported in the literature. The immunologic findings in both diseases are similar. We conclude that immunologic studies using frozen sections are probably of no help in differentiating between these two disorders when histologic findings are not conclusive.

摘要

本文报告一例狼疮性淋巴结炎并进行了冰冻切片免疫组织学研究。临床上,该患者有明确记录的系统性红斑狼疮(SLE),当全身淋巴结病迅速发展时,增加了恶性淋巴瘤诊断的可能性。组织学上,副皮质区坏死灶和苏木精小体的发现可诊断为SLE。未见粒细胞。应用于冰冻切片的单克隆抗体显示,在坏死副皮质区内及周围有两种主要细胞群:OKM1 +、Leu - M1 +组织细胞和OKT8 +、Leu - 4 + T细胞毒性/抑制细胞。在未发生坏死的淋巴结中,淋巴滤泡由多型性B细胞组成,滤泡间区为T细胞。Leu - 3a + Leu - 4 + T辅助/诱导细胞与T细胞毒性/抑制细胞的比例为3:1。由于狼疮性淋巴结炎可能与菊池和藤本组织细胞坏死性淋巴结炎极为相似,特别是在未发现苏木精小体的情况下,我们将该病例的结果与文献中报道的菊池和藤本组织细胞坏死性淋巴结炎病例的结果进行了比较。两种疾病的免疫结果相似。我们得出结论,当组织学结果不明确时,使用冰冻切片进行免疫研究可能无助于区分这两种疾病。

相似文献

1
Lupus lymphadenitis: report of a case with immunohistologic studies on frozen sections.狼疮性淋巴结炎:一例经冰冻切片免疫组织学研究的病例报告。
Hum Pathol. 1989 Mar;20(3):295-9. doi: 10.1016/0046-8177(89)90141-x.
2
Histology-Independent Signature Distinguishes Kikuchi-Fujimoto Disease/Systemic Lupus Erythematosus-Associated Lymphadenitis From Benign and Malignant Lymphadenopathies.组织学独立特征可区分组织细胞坏死性淋巴结炎/系统性红斑狼疮相关淋巴结炎与良恶性淋巴结病。
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Necrotizing lymphadenitis associated with systemic lupus erythematosus.与系统性红斑狼疮相关的坏死性淋巴结炎。
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Histiocytic necrotizing lymphadenitis, Kikuchi-Fujimoto's disease, associated with systemic lupus erythemotosus.组织细胞性坏死性淋巴结炎,即菊池-藤本病,与系统性红斑狼疮相关。
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Systemic lupus erythematosus with erythema multiforme-like lesions and histiocytic necrotizing lymphadenitis--a case report.伴有多形红斑样皮损和组织细胞坏死性淋巴结炎的系统性红斑狼疮——病例报告
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Necrotizing lymphadenitis: Kikuchi--Fujimoto disease alias lupus lymphadenitis?坏死性淋巴结炎:菊池-藤本病别名狼疮性淋巴结炎?
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Distinguishing lupus lymphadenitis from Kikuchi disease based on clinicopathological features and C4d immunohistochemistry.根据临床病理特征和 C4d 免疫组化鉴别狼疮性淋巴结炎与菊池病。
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Involvement of cell-mediated killing in apoptosis in histiocytic necrotizing lymphadenitis (Kikuchi-Fujimoto disease).细胞介导的杀伤作用在组织细胞坏死性淋巴结炎(菊池-藤本病)细胞凋亡中的作用。
Histopathology. 1996 Jan;28(1):41-8. doi: 10.1046/j.1365-2559.1996.267310.x.

引用本文的文献

1
Kikuchi's disease as a presenting feature of mixed connective tissue disease.菊池病作为混合性结缔组织病的首发表现
Clin Rheumatol. 1995 Jan;14(1):104-7. doi: 10.1007/BF02208094.
2
Kikuchi's disease in systemic lupus erythematosus: an independent or dependent event?
Clin Rheumatol. 1991 Mar;10(1):90-3. doi: 10.1007/BF02208041.
3
Histiocytic necrotising lymphadenitis in systemic lupus erythematosus.系统性红斑狼疮中的组织细胞坏死性淋巴结炎
Ann Rheum Dis. 1992 Jun;51(6):805-7. doi: 10.1136/ard.51.6.805.