Literature DB >> 9884699

Langerhans' cell histiocytosis and juvenile xanthogranuloma of the orbit. Clinicopathologic, CT, and MR imaging features.

A A Hidayat1, M F Mafee, N V Laver, S Noujaim.   

Abstract

The clinical, radiologic, and histopathologic features of two main disorders of the orbit are discussed. Group I, Langerhans cell histiocytosis (histiocytosis X, Class I), is caused by proliferation of X histiocytic Langerhans' cells. Group II is juvenile xanthogranuloma, and Class II is related to the proliferation of non-X histiocytic (monocyte-macrophage) cells. The two diseases are of unknown cause and differ in their clinical, radiologic, and histopathologic features.

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Year:  1998        PMID: 9884699     DOI: 10.1016/s0033-8389(05)70242-6

Source DB:  PubMed          Journal:  Radiol Clin North Am        ISSN: 0033-8389            Impact factor:   2.303


  2 in total

1.  Eosinophilic granuloma of the orbit: a paradox of aggressive destruction responsive to minimal intervention.

Authors:  Gerald J Harris; Kyung In Woo
Journal:  Trans Am Ophthalmol Soc       Date:  2003

2.  Imaging Features of Juvenile Xanthogranuloma of the Pediatric Head and Neck.

Authors:  D T Ginat; S O Vargas; V M Silvera; M S Volk; B A Degar; C D Robson
Journal:  AJNR Am J Neuroradiol       Date:  2016-01-07       Impact factor: 3.825

  2 in total

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