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Rapidly progressive obstructive jaundice due to Congo red negative amyloidosis.

作者信息

McClements B M, Shanks J H, Hill C M, Cameron C H, Callender M E

机构信息

Royal Victoria Hospital, Belfast.

出版信息

Ulster Med J. 1991 Oct;60(2):229-34.

PMID:1785159
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2448642/
Abstract
摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/8397d4ab10a3/ulstermedj00077-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/837f91f30a7f/ulstermedj00077-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/ceb264df9823/ulstermedj00077-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/8397d4ab10a3/ulstermedj00077-0109-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/837f91f30a7f/ulstermedj00077-0107-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/ceb264df9823/ulstermedj00077-0108-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8bf5/2448642/8397d4ab10a3/ulstermedj00077-0109-a.jpg

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本文引用的文献

1
Different morphologic aspects and clinical features in massive hepatic amyloidosis.
Digestion. 1984;29(3):138-45. doi: 10.1159/000199023.
2
DMSO and colchicine therapy in amyloid disease.二甲基亚砜和秋水仙碱治疗淀粉样变性疾病
Ann Rheum Dis. 1984 Jun;43(3):421-3. doi: 10.1136/ard.43.3.421.
3
Dizzy medical writing: Part II.令人头晕目眩的医学写作：第二部分。
South Med J. 1984 Jun;77(6):755-6. doi: 10.1097/00007611-198406000-00022.
原发性淀粉样变性表现为腹腔镜胆囊切除术后胆汁淤积性黄疸。
Case Rep Surg. 2015;2015:353818. doi: 10.1155/2015/353818. Epub 2015 Jun 7.
4
Amyloidosis (AL). Clinical and laboratory features in 229 cases.淀粉样变性（AL型）。229例患者的临床及实验室特征。
Mayo Clin Proc. 1983 Oct;58(10):665-83.
5
The liver in amyloidosis.
Digestion. 1974;10(1):40-51. doi: 10.1159/000197521.
6
Obstructive jaundice from hepatic amyloidosis in a patient with multiple myeloma.
Am J Hematol. 1985 Jul;19(3):277-9. doi: 10.1002/ajh.2830190309.
7
Response of primary hepatic amyloidosis to melphalan and prednisone: a case report and review of the literature.
Mayo Clin Proc. 1986 Mar;61(3):218-23. doi: 10.1016/s0025-6196(12)61853-9.
8
Hepatic amyloidosis (primary [AL], immunoglobulin light chain): the natural history in 80 patients.
Am J Med. 1988 Jul;85(1):73-80. doi: 10.1016/0002-9343(88)90505-0.
9
Cholestasis and liver failure with lambda-AL amyloidosis.伴有λ-AL淀粉样变性的胆汁淤积和肝衰竭。
Gut. 1987 Jul;28(7):903-6. doi: 10.1136/gut.28.7.903.
10
Severe intrahepatic cholestasis and rapidly progressive renal failure in a patient with immunocyte-related amyloidosis.
J Clin Gastroenterol. 1987 Apr;9(2):219-22. doi: 10.1097/00004836-198704000-00023.