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未表现为沃林格-科洛普病的局限性蕈样肉芽肿

Localized mycosis fungoides not manifesting as Woringer-Kolopp disease.

作者信息

Ringel E, Medenica M, Lorincz A

出版信息

Arch Dermatol. 1983 Sep;119(9):756-60.

PMID:6614964
Abstract

A 68-year-old man had a solitary, eczematiform lesion of two years' duration on the digital dorsal surface of his right foot. Despite its innocuous appearance, the lesion showed histologic characteristics of advanced, plaque-type mycosis fungoides. The patient's clinically benign yet histologically malignant disease manifestation is discussed. The distinction between localized mycosis fungoides and Woringer-Kolopp disease is also reviewed.

摘要

一名68岁男性在其右脚趾背侧有一个持续两年的孤立性湿疹样皮损。尽管其外观无害,但该皮损显示出晚期斑块型蕈样肉芽肿的组织学特征。讨论了该患者临床良性但组织学恶性的疾病表现。还回顾了局限性蕈样肉芽肿与沃林格-科洛普病之间的区别。

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1
Localized mycosis fungoides not manifesting as Woringer-Kolopp disease.未表现为沃林格-科洛普病的局限性蕈样肉芽肿
Arch Dermatol. 1983 Sep;119(9):756-60.
2
Localized mycosis fungoides with prominent epidermotropism: Woringer-Kolopp disease.
Arch Dermatol. 1977 Sep;113(9):1254-6.
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Woringer-Kolopp disease (localized pagetoid reticulosis) or unilesional mycosis fungoides? An analysis of eight cases with benign disease.沃林格-科洛普病(局限性蕈样肉芽肿性网状细胞增生症)还是单病灶蕈样肉芽肿?8例良性疾病分析
Arch Dermatol. 1995 Mar;131(3):325-9.
5
Clinicopathologic features and treatment outcomes in Woringer-Kolopp disease.
J Am Acad Dermatol. 2008 Oct;59(4):706-12. doi: 10.1016/j.jaad.2008.04.018. Epub 2008 Jun 11.
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[Epidermotropic reticulosis of the Woringer-Kolopp type (author's transl)].沃林格-科洛普型亲表皮性网状细胞增生病(作者译)
Dermatologica. 1979;159(2):101-14.
7
[Woringer and Kolopp's disease (author's transl)].[沃林格和科洛普病(作者译)]
Dermatologica. 1978;157(6):377-85.
8
[Differential diagnosis of the reticulosis described by Woringer and Kolopp].[沃林格和科洛普所描述的网状细胞增多症的鉴别诊断]
Dermatologica. 1970;140:Suppl 2:19-34.
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[Epidermotropic reticulosis (Woringer-Kolopp disease). Arguments in favor of a relationship with mycosis fungoides].[亲表皮性网状细胞增生症(沃林格-科洛普病)。支持与蕈样肉芽肿相关的论据]
Arch Belg Dermatol. 1974 Oct-Dec;30(4):187-94.
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The nature of mycosis fungoides.蕈样肉芽肿的本质。
Q J Med. 1986 Mar;58(227):281-93.