Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN 55905, USA.
Am J Surg Pathol. 2013 Jul;37(7):978-86. doi: 10.1097/PAS.0b013e318283099f.
The traditional model of hematopoiesis is based on unidirectional maturation of hematopoietic precursors into lineage-committed cells. However, recent studies indicate that mature B lymphocytes may demonstrate significant lineage plasticity. We and others have reported transdifferentiation of follicular lymphomas (FLs) into clonally related histiocytic/dendritic cell neoplasms. Here, we describe 2 patients with FL who developed clonally related Langerhans cell neoplasms. The first was a 52-year-old man diagnosed with FL, grade 1. He received immunochemotherapy and had stable disease for 8 years. He then developed increasing lymphadenopathy, and lymph node biopsy showed Langerhans cell sarcoma with no evidence of FL. The second patient was a 77-year-old woman who presented with lymphadenopathy, an abdominal mass, and pulmonary nodules. Lymph node biopsy showed both Langerhans cell histiocytosis and minimal involvement by FL, grade 1. In each case, a combination of immunoglobulin gene rearrangement and fluorescence in situ hybridization studies provided evidence to support a clonal relationship between the FL and Langerhans cell neoplasm. These cases provide striking examples of neoplastic transdifferentiation and expand the spectrum of lesions clonally identical to otherwise typical FL. Awareness of this phenomenon may aid in diagnosis when histologically dissimilar tumors arise synchronously or metachronously in patients with lymphoma.
造血的传统模式是基于造血前体单向成熟为谱系定向细胞。然而,最近的研究表明,成熟 B 淋巴细胞可能表现出显著的谱系可塑性。我们和其他人已经报道了滤泡性淋巴瘤(FL)向克隆相关组织细胞/树突状细胞肿瘤的转化。在这里,我们描述了 2 例发生克隆相关朗格汉斯细胞肿瘤的 FL 患者。第一例是一位 52 岁的男性,诊断为 FL,1 级。他接受了免疫化疗,病情稳定了 8 年。然后他出现了进行性淋巴结病,淋巴结活检显示朗格汉斯细胞肉瘤,没有 FL 的证据。第二例是一位 77 岁的女性,表现为淋巴结病、腹部肿块和肺结节。淋巴结活检显示朗格汉斯细胞组织细胞增生症和 1 级 FL 的最小受累。在每种情况下,免疫球蛋白基因重排和荧光原位杂交研究的结合提供了证据支持 FL 和朗格汉斯细胞肿瘤之间的克隆关系。这些病例提供了肿瘤转化的显著例子,并扩展了与其他典型 FL 克隆相同的病变谱。当淋巴瘤患者同时或异时出现组织学上不同的肿瘤时,这种现象的认识可能有助于诊断。