Tomasini Dario, Zampatti Clementina, Serio Giovanni
Department of Dermatology, Hospital of Busto Arsizio, Busto Arsizio, Italy.
J Cutan Pathol. 2009 Aug;36(8):887-91. doi: 10.1111/j.1600-0560.2008.01143.x.
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.
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。