Literature DB >> 18176190

Spontaneous regression of langerhans cell histiocytosis in a neonate with multiple bony lesions.

James McElligott1, Amy McMichael, Omar P Sangüeza, Evelyn Anthony, Donald Rose, Thomas W McLean.   

Abstract

We report the case of a newborn with Langerhans cell histiocytosis involving the skin and multiple bones. All lesions resolved without therapy. This case underscores the benefits of a conservative approach in the absence of risk organ involvement.

Mesh：

Year:  2008        PMID： 18176190     DOI： 10.1097/MPH.0b013e31815cc3d7

Source DB:  PubMed          Journal:  J Pediatr Hematol Oncol        ISSN： 1077-4114            Impact factor:   1.289


  3 in total

1.  IL-17A receptor expression differs between subclasses of Langerhans cell histiocytosis, which might settle the IL-17A controversy.

Authors:  Ichiro Murakami; Akira Morimoto; Takashi Oka; Satoshi Kuwamoto; Masako Kato; Yasushi Horie; Kazuhiko Hayashi; Jean Gogusev; Francis Jaubert; Shinsaku Imashuku; Lamia Abd Al-Kadar; Katsuyoshi Takata; Tadashi Yoshino
Journal:  Virchows Arch       Date:  2012-12-27       Impact factor: 4.064

2.  Recurrent BRAF mutations in Langerhans cell histiocytosis.

Authors:  Gayane Badalian-Very; Jo-Anne Vergilio; Barbara A Degar; Laura E MacConaill; Barbara Brandner; Monica L Calicchio; Frank C Kuo; Azra H Ligon; Kristen E Stevenson; Sarah M Kehoe; Levi A Garraway; William C Hahn; Matthew Meyerson; Mark D Fleming; Barrett J Rollins
Journal:  Blood       Date:  2010-06-02       Impact factor: 22.113

3.  Langerhans cell histiocytosis with hemorrhagic uveitis and exudative retinal detachment.

Authors:  Ranju Kharel Sitaula; Anadi Khatri
Journal:  Int Med Case Rep J       Date:  2018-03-26
  3 in total

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