首页> 外文期刊>Journal of cutaneous pathology >Concurrent cutaneous localization of Langerhans cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma in a patient with a history of chronic lymphocytic leukemia/small lymphocytic lymphoma
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Concurrent cutaneous localization of Langerhans cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma in a patient with a history of chronic lymphocytic leukemia/small lymphocytic lymphoma

机译:含有慢性淋巴细胞白血病史上患者朗格汉斯细胞肉瘤和慢性淋巴细胞白血病/小淋巴细胞淋巴瘤/小淋巴细胞淋巴瘤患者小淋巴细胞淋巴瘤的同时皮肤

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Abstract The phenomenon of histiocytic/dendritic cell sarcomas arising through transformation of a pre‐existed lymphoproliferative disease is called transdifferentiation. Langerhans cell sarcoma transdifferentiating from chronic lymphocytic leukemia/small lymphocytic lymphoma is extremely rare and all the reported cases were localized in lymph nodes. We present a case of concurrent cutaneous localization of Langerhans cell sarcoma and chronic lymphocytic leukemia/small lymphocytic lymphoma, in which the chronic lymphocytic leukemia/small lymphocytic lymphoma preceded the development of the Langerhans cell sarcoma. A cutaneous lesion from a 63‐year‐old patient with a history of chronic lymphocytic leukemia/small lymphocytic lymphoma was biopsied. The histologic examination revealed a mixture of two cell populations infiltrating diffusely the dermis. The first was composed of small lymphoid cells with somewhat monotonous appearance and mild nuclear atypia positive for PAX5, CD79a, CD20, CD23, CD5, and LEF1. The second was composed of large cells with abundant cytoplasm and pleomorphic nuclei. These cells were positive for CD1a, CD207, and S100 protein and exhibited a high mitotic rate and a high MIB‐1 immunostaining index. Therefore, two different entities, chronic lymphocytic leukemia/small lymphocytic lymphoma and Langerhans cell sarcoma, were detected in the same skin fragment. The patient died 3?years after initial diagnosis of chronic lymphocytic leukemia/small lymphocytic lymphoma.
机译:摘要通过预先存在的淋巴抑制性疾病转化而产生的组织细胞/树突状细胞肉瘤的现象称为转染细胞。来自慢性淋巴细胞白血病/小淋巴细胞淋巴瘤的朗格汉斯细胞肉瘤是极其罕见的,并且所有报道的病例都在淋巴结中局部化。我们提出了一种同时皮肤局部化的朗格汉斯肉瘤和慢性淋巴细胞白血病/小淋巴细胞淋巴瘤,其中慢性淋巴细胞白血病/小淋巴细胞淋巴瘤在朗格汉斯细胞肉瘤的发展之前。来自63岁患者的皮肤病因患者历史慢性淋巴细胞白血病/小淋巴细胞淋巴瘤进行活检。组织学检查揭示了两种细胞群渗透的混合物弥漫性的真皮。首先是由小淋巴细胞组成,具有稍微单调的外观和轻度核原型为PAX5,CD79A,CD20,CD23,CD5和lef1组成。第二个是由具有丰富细胞质和最亲核的大细胞组成。这些细胞对于CD1A,CD207和S100蛋白为阳性,并且表现出高丝分裂率和高MIB-1免疫染色指数。因此,在相同的皮肤片段中检测到两种不同实体,慢性淋巴细胞白血病/小淋巴细胞淋巴瘤和朗格汉斯蜂窝肉瘤。患者在初步诊断慢性淋巴细胞白血病/小淋巴细胞淋巴瘤后死亡3年。

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