Chilosi M, Menestrina F, Lestani M, Bonetti F, Scarpa A, Caligaris-Cappio F, Pizzolo G, Perini A, Fiore-Donati L
Istituto di Anatomia Patologica, Universitá di Verona, Italy.
Histol Histopathol. 1987 Jan;2(1):49-55.
A case of angiofollicular lymph node hyperplasia (Castleman's disease) characterized by monotypic (IgG+, lambda+) plasmacytosis is described. Fresh tissue was available and a thorough immunohistochemical analysis of lymphoid and non-lymphoid cells was performed on cryostat sections. Although lymphoid follicles were numerous and exhibited some abnormal features they did not appear part of the monoclonal cell proliferation. Follicular lymphocytes were mixtures of Kappa+ and lambda+ cells. Vessels penetrating within these abnormal follicles expressed reduced levels of FVIII and Leu-M5 antigens and exhibited thicker layer of collagen type IV. The analysis of T-cell subsets showed a normal (3:1) T4/T8 ratio. This case extends to the mixed variant of hyaline-vascular Castleman's disease, the neoplastic potential previously associated to the plasma cell variant of the disease.
描述了一例以单型(IgG +,λ +)浆细胞增多为特征的血管滤泡性淋巴结增生(Castleman病)。有新鲜组织可用,并对冷冻切片上的淋巴样和非淋巴样细胞进行了全面的免疫组织化学分析。尽管淋巴滤泡众多并表现出一些异常特征,但它们似乎不是单克隆细胞增殖的一部分。滤泡淋巴细胞是κ +和λ +细胞的混合物。穿透这些异常滤泡的血管表达的FVIII和Leu - M5抗原水平降低,并表现出较厚的IV型胶原层。T细胞亚群分析显示T4/T8比值正常(3:1)。该病例扩展到透明血管型Castleman病的混合型,此前该病的浆细胞型具有肿瘤形成潜能。