A case of fatal intrahepatic cholestasis with primary AL amyloidosis: is early diagnosis possible?

[1]  G. Gregorini,et al.  Liver involvement with rapidly progressive course in light chain (AL) amyloidosis: distinguishing features at presentation. Experience of a single center , 2011, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

[2]  D. Seldin,et al.  Amyloidosis: pathogenesis and new therapeutic options. , 2011, Journal of clinical oncology : official journal of the American Society of Clinical Oncology.

[3]  Z. Younossi,et al.  When and how to evaluate mildly elevated liver enzymes in apparently healthy patients , 2010, Cleveland Clinic Journal of Medicine.

[4]  H. Ishibashi,et al.  A case of prominent hepatic cholestasis developing to hepatic failure in lambda-AL amyloidosis , 1991, Gastroenterologia Japonica.

[5]  R. Miquel,et al.  Development of rapidly progressive liver light chain deposition under VAD chemotherapy in multiple myeloma , 2006, European journal of haematology.

[6]  R. Fonseca,et al.  Immunoglobulin light chain variable (V) region genes influence clinical presentation and outcome in light chain-associated amyloidosis (AL). , 2003, Blood.

[7]  G. Palladini,et al.  Hepatic amyloidosis with light chain deposition disease. A rare association. , 2000, Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver.

[8]  R. Kyle,et al.  Primary systemic amyloidosis: clinical and laboratory features in 474 cases. , 1995, Seminars in hematology.

[9]  A. Gimson,et al.  Primary amyloidosis and severe intrahepatic cholestatic jaundice. , 1994, Gut.

[10]  P. Heitz,et al.  Primäre Amyloidose der Leber , 1992 .

[11]  M. Spycher,et al.  [Primary amyloidosis of the liver]. , 1992, Deutsche medizinische Wochenschrift.

[12]  D. Lieberman,et al.  "Isolated" elevation of alkaline phosphatase: significance in hospitalized patients. , 1990, Journal of clinical gastroenterology.

[13]  R. Kyle,et al.  Hepatic amyloidosis (primary [AL], immunoglobulin light chain): the natural history in 80 patients. , 1988, The American journal of medicine.

[14]  W. Romen,et al.  [Jaundice in AL-amyloidosis in a 54-year-old patient]. , 1987, Medizinische Klinik.

[15]  F. Konikoff,et al.  Cholestasis and liver failure with lambda-AL amyloidosis. , 1987, Gut.

[16]  Kyle Ra,et al.  Amyloidosis (AL). Clinical and laboratory features in 229 cases. , 1983 .