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THE DIAGNOSIS: Primary Cutaneous Anaplastic Large Cell Lymphoma

机译:诊断:初级皮肤包塑大细胞淋巴瘤

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摘要

Primary cutaneous CD30+ lymphoproliferative disorders encompass lymphomatoid papulosis and primary cutaneous anaplastic large cell lymphoma (PCALCL) as well as borderline cases. Primary cutaneous anaplastic large cell lymphoma is a rare disease that is more common in white patients with slight male predominance and median age at diagnosis of 61 years.1 Prognosis is excellent, with a 90% survival rate at 10 years. Although lesions spontaneously regress in 6% to 22% of cases, complete resolution is rare.2 Clinically, the classic presentation is a solitary, rapidly growing, flesh-colored, erythematous nodule or plaque on the arms and legs or trunk, often with ulceration. Proper diagnosis requires clinical, histopathologic, and immuno- phenotypic correlation.
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    《Cutis》 |2018年第2期|共6页
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  • 正文语种 eng
  • 中图分类 皮肤病学与性病学;
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