Pina-Oviedo Sergio, Miranda Roberto N, Lin Pei, Manning John T, Medeiros L Jeffrey
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.
Department of Hematopathology, The University of Texas MD Anderson Cancer Center, Houston, TX 77030.
Hum Pathol. 2017 Oct;68:136-146. doi: 10.1016/j.humpath.2017.08.024. Epub 2017 Sep 2.
Follicular lymphoma (FL) with features reminiscent of hyaline-vascular Castleman disease (CD) is an unusual morphologic variant that may create diagnostic difficulties. To our knowledge, only 5 cases of this variant have been reported. We describe the clinicopathologic features of 6 cases including 2 men and 4 women with a median age of 63 years (range, 41-77). Morphologically, all lymph node biopsy specimens showed at least a focal area of conventional FL; 4 cases showed neoplastic follicles with hyalinized blood vessels penetrating into germinal centers (lollipop-like lesions); 4 cases had interfollicular areas with increased vascular stroma; 2 cases showed small neoplastic follicles with prominent, onionskin-like mantle zones; and 1 case showed 2 or more germinal centers within follicles (twinning). The small neoplastic follicles were more cellular than lymphocyte-depleted follicles of true hyaline-vascular CD, and the interface between germinal centers and mantle zones was ill defined. No cases showed dysplastic follicular dendritic cells. Immunohistochemistry for BCL-2 was positive in all 6 cases. Flow cytometry immunophenotypic analysis showed a monotypic B-cell population in 2 of 3 cases assessed. Conventional cytogenetic or fluorescence in situ hybridization studies performed in 3 cases showed t(14;18)(q32;q21) or IGH-BCL2, supporting the diagnosis of FL. The cases presented here add clinicopathologic data to the few cases of FL with hyaline-vascular CD-like features reported previously in the literature. Distinguishing this variant of FL from hyaline-vascular CD is important given the differences in treatment and prognosis of patients with each disease.
具有类似透明血管型Castleman病(CD)特征的滤泡性淋巴瘤(FL)是一种不常见的形态学变异型,可能会造成诊断困难。据我们所知,仅有5例该变异型的病例被报道。我们描述了6例患者的临床病理特征,其中包括2名男性和4名女性,中位年龄为63岁(范围41 - 77岁)。形态学上,所有淋巴结活检标本均显示至少有一个传统FL的局灶区域;4例显示肿瘤性滤泡伴有透明化血管穿入生发中心(棒棒糖样病变);4例有滤泡间区域血管间质增多;2例显示小的肿瘤性滤泡伴有显著的洋葱皮样套区;1例显示滤泡内有2个或更多生发中心(孪生现象)。这些小的肿瘤性滤泡比真正透明血管型CD的淋巴细胞消减性滤泡细胞更多,且生发中心与套区之间的界面不清晰。所有病例均未显示发育异常的滤泡树突状细胞。BCL - 2免疫组化在所有6例中均为阳性。在评估的3例中,2例流式细胞术免疫表型分析显示为单克隆B细胞群体。3例进行的传统细胞遗传学或荧光原位杂交研究显示t(14;18)(q32;q21)或IGH - BCL2,支持FL的诊断。本文报道的病例为先前文献中报道的少数具有透明血管型CD样特征的FL病例补充了临床病理资料。鉴于这两种疾病患者的治疗和预后存在差异,将这种FL变异型与透明血管型CD区分开来很重要。