Self-healing Langerhans cell histiocytosis (Hashimoto-Pritzker disease): two Tunisian cases

被引：0

作者：

Belhadjali, H. ^{[1
]}

Mohamed, M. ^{[1
]}

Mahmoudi, H. ^{[1
]}

Youssef, M. ^{[1
]}

Moussa, A. ^{[1
]}

Chouchane, S. Achour ^{[1
]}

Chouchane, C. ^{[1
]}

Zakhama, A. ^{[1
]}

Zili, J. ^{[1
]}

机构：

[1] Fattouma Bourguiba Hosp, Dept Dermatol, Monastir 5000, Tunisia

来源：

ACTA DERMATOVENEROLOGICA ALPINA PANNONICA ET ADRIATICA | 2008年 / 17卷 / 04期

关键词：

histiocytosis; Langerhans cell; self-healing; Hashimoto-Pritzker disease; childhood;

D O I：

暂无

中图分类号：

R75 [皮肤病学与性病学];

学科分类号：

100206 ;

摘要：

Self-healing Langerhans cell histiocytosis (SHLCH) is a rare self-limited variant of Langerhans cell histiocytosis that presents at birth or during the neonatal period. It was first described by Hashimoto and Pritzker in 1973. Subsequently, more than 70 cases have been reported in the literature. Regarding age of onset, SHLCH should be divided into congenital SHLCH and rare late-onset type. We report here two additional cases of SHLCH in Tunisian infants. We emphasize the need for long-term follow-up in such patients.

引用

页码：188 / 192

页数：5

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