PRIMARY HEPATIC AMYLOIDOSIS WITH SEVERE CHOLESTASIS: A CASE REPORT

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GHALAMKARI MARZIYE; KHATUNI MAHDI; TAHER MOHAMMAD; KHANIKI MAHMOOD

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Journal Paper

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Journal: GOVARESH JOURNAL Year:2016 | Volume:21 | Issue:1 Page(s): 76-80

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Title

PRIMARY HEPATIC AMYLOIDOSIS WITH SEVERE CHOLESTASIS: A CASE REPORT

Author(s)

GHALAMKARI MARZIYE | KHATUNI MAHDI | TAHER MOHAMMAD | KHANIKI MAHMOOD | Issue Writer Certificate

Keywords

INTRAHEPATIC CHOLESTASIS

PRIMARY AMYLOIDOSIS

LIVER AMYLOIDOSIS

Abstract

Despite the fact that hepatic involvement is frequently seen in systemic PRIMARY AMYLOIDOSIS, major hepatic symptoms as primary manifestation and severe impaired liver function are rare. Herein, we report a 38-year-old woman with primary hepatic amyloidosis, and severe portal hypertension. The patient had ascites and markedly elevated alkaline phosphatase level at presentation. She had a rapid downhill course resulting in death. In case of an unexplained INTRAHEPATIC CHOLESTASIS or portal hypertension the possibility of amyloidosis should be considered and a Congo red staining should be performed.

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APA: Copy

GHALAMKARI, MARZIYE, KHATUNI, MAHDI, TAHER, MOHAMMAD, & KHANIKI, MAHMOOD. (2016). PRIMARY HEPATIC AMYLOIDOSIS WITH SEVERE CHOLESTASIS: A CASE REPORT. GOVARESH JOURNAL, 21(1), 76-80. SID. https://sid.ir/paper/696278/en

Vancouver: Copy

GHALAMKARI MARZIYE, KHATUNI MAHDI, TAHER MOHAMMAD, KHANIKI MAHMOOD. PRIMARY HEPATIC AMYLOIDOSIS WITH SEVERE CHOLESTASIS: A CASE REPORT. GOVARESH JOURNAL[Internet]. 2016;21(1):76-80. Available from: https://sid.ir/paper/696278/en

IEEE: Copy

MARZIYE GHALAMKARI, MAHDI KHATUNI, MOHAMMAD TAHER, and MAHMOOD KHANIKI, “PRIMARY HEPATIC AMYLOIDOSIS WITH SEVERE CHOLESTASIS: A CASE REPORT,” GOVARESH JOURNAL, vol. 21, no. 1, pp. 76–80, 2016, [Online]. Available: https://sid.ir/paper/696278/en

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