Langerhans cell histiocytosis

Langerhans cell histiocytosis (LCH) is a systemic disease associated with the proliferation and accumulation (usually in granulomas) of Langerhans cells in various tissues.

Cirrhosis

A chronic disorder of the liver in which liver tissue becomes scarred and is partially replaced by regenerative nodules and fibrotic tissue resulting in loss of liver function.


合計: 5

                       


（表示件数）
PMID (PMCID)
16476286
 MALE Infant
[Xanthomas in a patient with Langerhans cell histiocytosis and liver cirrhosis].
Calzado L, Postigo C, Prado Sanchez-Caminero M, Sanz H, Guerra A, Vanaclocha F, Rodriguez-Peralto JL.
Actas Dermosifiliogr. 2005;96(8):518-21.
[Xanthomas in a patient with Langerhans cell histiocytosis and liver cirrhosis].
3264377
 MALE
Liver cirrhosis in histiocytosis X.
Pirovino M, Jeanneret C, Lang RH, Luisier J, Bianchi L, Spichtin H.
Liver. 1988;8(5):293-8.
Cirrhosis of the liver was diagnosed in an 18-year-old man with histiocytosis X. Electron microscopy and immunohistochemistry revealed infiltration of the liver by the typical cellular elements of histiocytosis X. Endoscopic retrograde cholangiography showed alterations resembling those of sclerosing cholangitis.
3264377
 MALE
Liver cirrhosis in histiocytosis X.
Pirovino M, Jeanneret C, Lang RH, Luisier J, Bianchi L, Spichtin H.
Liver. 1988;8(5):293-8.
Thus, cirrhosis of liver can be a main and potentially fatal manifestation of histiocytosis X beyond the pediatric age range.
3264377
 MALE
Liver cirrhosis in histiocytosis X.
Pirovino M, Jeanneret C, Lang RH, Luisier J, Bianchi L, Spichtin H.
Liver. 1988;8(5):293-8.
Liver cirrhosis in histiocytosis X.
3264377
 MALE
Liver cirrhosis in histiocytosis X.
Pirovino M, Jeanneret C, Lang RH, Luisier J, Bianchi L, Spichtin H.
Liver. 1988;8(5):293-8.
Cirrhosis of the liver was diagnosed in an 18-year-old man with histiocytosis X. Electron microscopy and immunohistochemistry revealed infiltration of the liver by the typical cellular elements of histiocytosis X. Endoscopic retrograde cholangiography showed alterations resembling those of sclerosing cholangitis.