Literature DB >> 6975154

"Pure" cutaneous histiocytosis-X.

S L Wolfson, F Botero, S Hurwitz, H A Pearson.   

Abstract

The case histories of two young children who experienced skin rashes involving various areas of the body are reported. The diagnosis of pure cutaneous histiocytosis-X was established after extensive studies revealed no other organ involvement. The patients were treated with oral corticosteroids. Currently, both children are in good health, show no evidence of disease, and have been followed over a four-to-five-year period. Therapy with corticosteroids may not be indicated with pure cutaneous histiocytosis-X unless there is evidence of extracutaneous dissemination or rapid progression of the disease.

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Year:  1981        PMID: 6975154     DOI: 10.1002/1097-0142(19811115)48:10<2236::aid-cncr2820481019>3.0.co;2-g

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  3 in total

1.  Diabetes insipidus for five years preceding the diagnosis of hypothalamic Langerhans cell histiocytosis.

Authors:  P F Catalina; M Rodr'iguez Garc'ia; C de la Torre; C P'aramo; R V Garc'ia-Mayor
Journal:  J Endocrinol Invest       Date:  1995-09       Impact factor: 4.256

2.  Spontaneous healing of Langerhans cell histiocytosis (histiocytosis X).

Authors:  L Corbeel; E Eggermont; J Desmyter; I Surmont; R De Vos; C De Wolf-Peeters; C Cobbaert; A Eykens
Journal:  Eur J Pediatr       Date:  1988-10       Impact factor: 3.183

3.  Flow-cytometric DNA content of histiocytosis X (Langerhans cell histiocytosis).

Authors:  M S Rabkin; C T Wittwer; C R Kjeldsberg; M W Piepkorn
Journal:  Am J Pathol       Date:  1988-05       Impact factor: 4.307

  3 in total

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