| Literature DB >> 11169892 |
N Ghosal1, K Kapila, S Kakkar, K Verma.
Abstract
Langerhans cell histiocytosis (LCH) is a disease of unknown etiology characterized by a proliferation of histiocytic cells resembling the integumentary cells bearing the name of Langerhans cells. LCH can be unifocal or multifocal, with one- or many-organ involvement. We present a case of LCH diagnosed in the cerebrospinal fluid of a patient with generalized lymphadenopathy and central nervous system involvement. Copyright 2001 Wiley-Liss, Inc.Entities:
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Year: 2001 PMID： 11169892 DOI： 10.1002/1097-0339(200102)24:2<123::aid-dc1023>3.0.co;2-u
Source DB: PubMed Journal: Diagn Cytopathol ISSN： 1097-0339 Impact factor: 1.582