[淋巴瘤样丘疹病——预后不确定的假性淋巴瘤]
[Lymphomatoid papulosis--pseudolymphoma with uncertain prognosis].
作者信息
Hagedorn M, Gross G, Strasser W
出版信息
Z Hautkr. 1986 Apr 15;61(8):549-55.
PMID:3716531
Abstract
On account of its distinct clinical and histological picture, lymphomatoid papulosis (l.p.) is mostly considered an entity. A 70-year-old patient with l.p. is described. Histologically, there were similarities to the granulomatous type of pseudolymphoma. The oral treatment with penicillin for 4 weeks was successful, but we cannot exclude a spontaneous remission.
摘要
鉴于其独特的临床和组织学表现，淋巴瘤样丘疹病（L.P.）大多被视为一种独立的疾病实体。本文描述了一名70岁的淋巴瘤样丘疹病患者。组织学上，其表现与肉芽肿型假性淋巴瘤相似。口服青霉素治疗4周取得了成功，但我们不能排除自发缓解的可能性。
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