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伴有大量胞质透明的套区淋巴细胞的Castleman病累及皮肤:病例报告

Castleman's disease with numerous mantle zone lymphocytes with clear cytoplasm involving the skin: case report.

作者信息

Tomasini Dario, Zampatti Clementina, Serio Giovanni

机构信息

Department of Dermatology, Hospital of Busto Arsizio, Busto Arsizio, Italy.

出版信息

J Cutan Pathol. 2009 Aug;36(8):887-91. doi: 10.1111/j.1600-0560.2008.01143.x.

DOI:10.1111/j.1600-0560.2008.01143.x
PMID:19586499
Abstract

Castleman's disease (CD) is an unusual lymphoid hyperplasia occurring in the mediastinal lymph nodes and, less frequently, in the neck lymph nodes. CD is classified clinically into a unicentric and a multicentric type, whereas three histomorphological variants are recognized: the hyaline vascular type, the intermediate type and the plasma cell type. We report the clinical and pathological features of a 54-year-old female suffering with multiple sclerosis and developing a lymph node hyaline-vascular type CD relapsing in the skin after 24 months. Histological features showed a nodular dermatitis with atrophic germinal centers and an 'onion skin' rimming of lymphocytes in the mantle zone with numerous mantle zone lymphocytes with clear cytoplasm, with a CD20+, CD79a+, IgM+, IgG-, IgA-, CD5-, CD10-, CD43-, CD45RO-, bcl-2+ and bcl-6- phenotype with polytypic nature supporting the diagnosis of lymphoid variant of hyaline-vascular CD. This case shows that skin CD recapitulates all the histological variants of lymph node CD. Considering the many similarities between the present case and the primary cutaneous marginal zone lymphoma, it is important to bear in mind this atypical lymphoproliferative disorder in order to avoid overdiagnosis and overtreatment.

摘要

卡斯特曼病(CD)是一种发生于纵隔淋巴结的罕见淋巴组织增生性疾病,较少见于颈部淋巴结。CD临床上分为单中心型和多中心型,组织形态学上有三种类型:透明血管型、中间型和浆细胞型。我们报告了一名54岁患有多发性硬化症的女性患者的临床和病理特征,该患者发生了淋巴结透明血管型CD,24个月后在皮肤复发。组织学特征显示为结节性皮炎,生发中心萎缩,套区有淋巴细胞呈“洋葱皮样”环绕,套区有大量细胞质清晰的淋巴细胞,其表型为CD20+、CD79a+、IgM+、IgG-、IgA-、CD5-、CD10-、CD43-、CD45RO-、bcl-2+和bcl-6-,具有多型性,支持透明血管型CD的淋巴样变异型诊断。该病例表明皮肤CD重现了淋巴结CD的所有组织学类型。考虑到本病例与原发性皮肤边缘区淋巴瘤有许多相似之处,为避免过度诊断和过度治疗,牢记这种非典型淋巴增殖性疾病很重要。

相似文献

1
Castleman's disease with numerous mantle zone lymphocytes with clear cytoplasm involving the skin: case report.伴有大量胞质透明的套区淋巴细胞的Castleman病累及皮肤:病例报告
J Cutan Pathol. 2009 Aug;36(8):887-91. doi: 10.1111/j.1600-0560.2008.01143.x.
2
Lymphoid variant of hyaline vascular Castleman's disease containing numerous mantle zone lymphocytes with clear cytoplasm.透明血管型Castleman病的淋巴细胞样变型,含有众多胞质透明的套区淋巴细胞。
APMIS. 2005 Jan;113(1):75-80. doi: 10.1111/j.1600-0463.2005.apm1130112.x.
3
The immunophenotypic patterns of follicle centre and mantle zone in Castleman's disease.Castleman病中滤泡中心和套区的免疫表型模式。
Singapore Med J. 2003 Apr;44(4):185-91.
4
Primary cutaneous CD5+ marginal zone B-cell lymphoma resembling the plasma cell variant of Castleman's disease. Case report.原发性皮肤CD5+边缘区B细胞淋巴瘤,类似卡斯特曼病的浆细胞变异型。病例报告。
APMIS. 2007 Dec;115(12):1426-31. doi: 10.1111/j.1600-0463.2007.00797.x.
5
Progressive transformation of germinal center presenting with histological features of hyaline-vascular type of Castleman's disease.生发中心进行性转化,呈现透明血管型Castleman病的组织学特征。
APMIS. 2005 Apr;113(4):288-95. doi: 10.1111/j.1600-0463.2005.apm_08.x.
6
Expression of EGFR and follicular dendritic markers in lymphoid follicles from patients with Castleman's disease.Castleman病患者淋巴滤泡中表皮生长因子受体(EGFR)及滤泡树突状细胞标志物的表达
Oncol Rep. 2008 Oct;20(4):851-6.
7
Idiopathic multicentric Castleman's disease. A clinicopathologic and immunohistochemical study of five cases.特发性多中心Castleman病。5例临床病理及免疫组化研究
Pathol Res Pract. 2005;201(4):325-32. doi: 10.1016/j.prp.2005.01.006.
8
Castleman's disease.卡斯尔曼病
Adv Clin Path. 1999 Jan-Apr;3(1-2):11-22.
9
Castleman's disease of the leptomeninges--immunohistochemical findings in 2 cases.柔脑膜Castleman病——2例免疫组化结果
Clin Neuropathol. 2002 Nov-Dec;21(6):278-83.
10
Multicentric Castleman's disease in association with Kaposi's sarcoma.多中心性卡斯特曼病合并卡波西肉瘤
Appl Pathol. 1989;7(2):105-10.

引用本文的文献

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Castleman's Disease with Cutaneous Involvement Manifestating as Multiple Violaceous Plaques on Entire Body.伴有皮肤受累的Castleman病表现为全身多发紫蓝色斑块。
Ann Dermatol. 2011 Oct;23(Suppl 2):S169-74. doi: 10.5021/ad.2011.23.S2.S169. Epub 2011 Oct 31.