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首页> 外文期刊>American Journal of Dermatopathology >Primary cutaneous CD8(+) small- to medium-sized lymphoproliferative disorder in extrafacial sites: clinicopathologic features and concept on their classification.
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Primary cutaneous CD8(+) small- to medium-sized lymphoproliferative disorder in extrafacial sites: clinicopathologic features and concept on their classification.

机译:面部部位的原发性皮肤CD8(+)中小型淋巴组织增生性疾病:临床病理特征和分类概念。

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摘要

Three cases with CD8+ small- to medium-sized lymphoproliferations in the skin at extrafacial sites are described. Clinically, the patients presented with papulonodular or plaque-like lesions without preceding patches. Histopathologically, nonepidermotropic nodular or diffuse infiltrates were composed of small- to medium-sized pleomorphic lymphocytes, which expressed CD8 (more than 80% of the cells) and granzyme B (60%-70% of the cells), but were negative for CD4, CD30, and CD56. There was no association with Epstein-Barr virus. A clonal T-cell population was detected in 2 patients. Staging examinations did not reveal extracutaneous involvement. The 2 patients with solitary lesions underwent complete remission after radiation therapy, whereas 1 patient developed multifocal lesions and several recurrences. These CD8+ small- to medium-sized lymphoproliferations of the skin at extrafacial sites may belong to a spectrum of phenotypically and prognostically heterogeneous cutaneous small- to medium-sized lymphoid proliferations, which are characterized by an indolent course in most patients.
机译:描述了三例在面部部位皮肤中出现CD8 +中小型淋巴组织增生的病例。临床上,患者出现了丘疹或斑块样病变,而没有先前的斑块。组织病理学上,非促汗液性结节性或弥漫性浸润由小至中型多形性淋巴细胞组成,其表达CD8(占细胞的80%以上)和粒酶B(占细胞的60%-70%),但对CD4呈阴性,CD30和CD56。与爱泼斯坦-巴尔病毒没有关联。在2例患者中检测到克隆性T细胞群体。分期检查未发现皮肤外受累。 2例孤立病变的患者在放射治疗后完全缓解,而1例出现多灶性病变并多次复发。这些CD8 +面外皮肤的小到中型淋巴组织增生可能属于表型和预后异质的皮肤小到中型淋巴增生谱,其特征是大多数患者的病程缓慢。

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