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首页> 外文期刊>American Journal of Dermatopathology >Primary Cutaneous Marginal Zone Lymphoma in Children: A Report of 3 Cases and Review of the Literature
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Primary Cutaneous Marginal Zone Lymphoma in Children: A Report of 3 Cases and Review of the Literature

机译:儿童原发性皮肤边缘区淋巴瘤3例报告并文献复习

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摘要

Primary cutaneous marginal zone lymphoma (PCMZL) is one of the most common cutaneous B-cell lymphomas. It affects mostly patients in their fourth decade and manifests with multifocal nodules mostly on the arms and upper trunk in more than half of the patients. PCMZL is, however, rare in children and adolescents, with only 20 cases reported in patients aged 20 and younger. The authors present 3 cases of PCMZL in teenagers. The patients were 2 girls aged 18 and 13 and a 17-year-old boy. Two patients presented with multiple lesions involving various anatomic sites, whereas in 1 patient, 2 small closely opposed papules on the abdomen were seen. Histopathologically, the characteristic appearance of PCMZL was found in 3 of 4 specimens, with nodular infiltrates composed of small lymphocytes in the interfollicular compartment, reactive germinal centers, and plasma cells in small clusters mainly at the periphery of the infiltrates, whereas 1 specimen showed a dense lymphocytic infiltrate with small granulomas. Clonality was demonstrated by monotypic immunoglobulin light chain expression and/or monoclonal rearrangement of the immunoglobulin heavy chain genes. No Borrelia burgdorferi was identified on serology or by polymerase chain reaction in any of the cases. Treatment included excision or administration of antibiotics with complete remission in all the 3 patients indicating that PCMZL in children and young adolescents follows the same indolent course with a tendency for recurrences, but excellent prognosis as in adults. The pertinent literature on PCZL in childhood and adolescence is reviewed.
机译:原发性皮肤边缘区淋巴瘤(PCMZL)是最常见的皮肤B细胞淋巴瘤之一。它影响到了第四个十年中的大多数患者,并且在一半以上的患者中,多灶性结节表现在手臂和上躯干上。然而,PCMZL在儿童和青少年中很少见,只有20例在20岁及以下的患者中报告。作者介绍了3例青少年PCMZL。患者是2名18和13岁的女孩和17岁的男孩。 2例患者出现涉及多个解剖部位的多处病变,而1例患者腹部可见2个紧密面对的小丘疹。在组织病理学上,在4个标本中有3个发现了PCMZL的特征性外观,其结节性浸润由小细胞分布在小泡间室,反应生发中心和浆细胞小簇中,主要在浸润周围,而1个标本显示小颗粒肉芽肿浸润致密淋巴细胞。通过单型免疫球蛋白轻链表达和/或免疫球蛋白重链基因的单克隆重排证明了克隆性。在任何情况下,血清学或通过聚合酶链反应均未鉴定出伯氏疏螺旋体。治疗包括对3例患者全部切除或给予抗生素治疗,并完全缓解,这表明儿童和青少年PCMZL的病程相同,有复发的趋势,但预后与成人相似。综述了有关儿童期和青春期PCZL的文献。

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