| Literature DB >> 11734951 |
C W König1, C Pfannenberg, J Trübenbach, C Remy, G M Böhmer, P Ruck, C D Claussen.
Abstract
Langerhans' cell histiocytosis (LCH) is a disorder of histiocytic proliferation that primarily affects infants. Imaging findings of a rare case of lung and liver involvement in an adult are presented. High-resolution computed tomography (HRCT) of the lungs showed confluent thin-walled cystic air spaces compatible with advanced LCH. Liver CT and MRI revealed unspecific signs of fatty infiltration. Irregular widening of peripheral bile ducts was displayed in breath-hold MR cholangiography. This pattern is considered characteristic for sclerosing cholangitis and should support the diagnosis of LCH in case of concomitant cystic pulmonary disease, even in adult patients.Entities:
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Year: 2001 PMID: 11734951 DOI: 10.1007/s003300100835
Source DB: PubMed Journal: Eur Radiol ISSN: 0938-7994 Impact factor: 5.315