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首页> 外文期刊>American Journal of Dermatopathology >Composite Mantle Cell and Primary Cutaneous Anaplastic Large Cell Lymphoma: Case Report and Review of the Literature
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Composite Mantle Cell and Primary Cutaneous Anaplastic Large Cell Lymphoma: Case Report and Review of the Literature

机译:复合套细胞和原发性皮肤间变性大细胞淋巴瘤:病例报告和文献复习。

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摘要

We describe the first reported occurrence of a composite cutaneous lymphoma involving a mantle cell lymphoma (MCL) and primary cutaneous anaplastic large cell lymphoma. The lesion occurred in a 76-year-old man with longstanding MCL who developed nodular skin lesions on his trunk and extremities. Biopsy revealed a CD30-positive lymphoma with pathological features characteristic of cutaneous anaplastic large cell lymphoma in the superficial dermis and a subjacent deposit of MCL in the deep dermis and subcutaneous adipose tissue. Immunophenotyping demonstrated T versus B lymphoid origin, respectively, for the 2 neoplasms, and fluorescence in situ hybridization demonstrated an 11;14 chromosomal translocation exclusively in the MCL. These results argue that the lymphomas represented clonally distinct neoplasms. Our case illustrates the extreme diversity associated with the cutaneous manifestations of lymphoid neoplasia and in particular of composite lymphomas, which present diagnostic challenges for clinicians and pathologists alike.
机译:我们描述了首次报告的复合皮肤淋巴瘤的发生,其中涉及套细胞淋巴瘤(MCL)和原发性皮肤间变性大细胞淋巴瘤。病灶发生在一个76岁的MCL病患,他的长期病情在其躯干和四肢上形成了结节性皮肤病。活检显示CD30阳性淋巴瘤具有病理特征,表皮真皮具有皮肤变性间变性大细胞淋巴瘤,深层真皮和皮下脂肪组织中有MCL的下沉积。免疫分型表明2种肿瘤分别是T与B淋巴样起源,而荧光原位杂交表明MCL仅具有11; 14染色体易位。这些结果表明,淋巴瘤代表了克隆不同的肿瘤。我们的病例说明了与淋巴瘤形成,特别是复合淋巴瘤的皮肤表现有关的极端多样性,这对临床医生和病理学家都提出了诊断挑战。

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