Response of Bortezomib Chemotherapy in Hepatic Amyloidosis

Amyloidosis is a rare disorder with a wide spectrum of presentations and anomalies. It is subdivided into 2 broad categories based on protein deposition; primary and secondary amyloidosis. It can present as a single-organ involvement or as a diffuse infiltrative multi-organ process. Isolated hepatic...

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Main Authors: Syed M. Hasan MD, Nida N. Ahmed MD, Zunirah Ahmed MD, Allan Seibert MD
Format: Article
Language:English
Published: SAGE Publishing 2018-03-01
Series:Journal of Investigative Medicine High Impact Case Reports
Online Access:https://doi.org/10.1177/2324709618760079
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spelling doaj-a4d27e0b2c6e4150b0c4fe4c78a8952c2020-11-25T02:52:30ZengSAGE PublishingJournal of Investigative Medicine High Impact Case Reports2324-70962018-03-01610.1177/2324709618760079Response of Bortezomib Chemotherapy in Hepatic AmyloidosisSyed M. Hasan MD0Nida N. Ahmed MD1Zunirah Ahmed MD2Allan Seibert MD3University of Alabama at Birmingham, Montgomery, AL, USAUniversity of Alabama at Birmingham, Montgomery, AL, USAUniversity of Alabama at Birmingham, Montgomery, AL, USAUniversity of Alabama at Birmingham, Montgomery, AL, USAAmyloidosis is a rare disorder with a wide spectrum of presentations and anomalies. It is subdivided into 2 broad categories based on protein deposition; primary and secondary amyloidosis. It can present as a single-organ involvement or as a diffuse infiltrative multi-organ process. Isolated hepatic amyloidosis presentation is a rare phenomenon that develops due to insoluble amyloid deposition in liver. Its clinical presentation is usually vague and ranges from mild hepatomegaly with elevated liver enzymes to acute liver failure and hepatic rupture. Currently, there are scarce data available regarding treatment options for biopsy-proven hepatic amyloidosis. In this review article, we present an interesting case of hepatic amyloidosis and its poor outcome to new molecular targeted chemotherapy. Furthermore, we aim to review current and future diagnostic tools for early detection and advancements in targeted chemotherapeutics options available for hepatic amyloidosis.https://doi.org/10.1177/2324709618760079
collection DOAJ
language English
format Article
sources DOAJ
author Syed M. Hasan MD
Nida N. Ahmed MD
Zunirah Ahmed MD
Allan Seibert MD
spellingShingle Syed M. Hasan MD
Nida N. Ahmed MD
Zunirah Ahmed MD
Allan Seibert MD
Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
Journal of Investigative Medicine High Impact Case Reports
author_facet Syed M. Hasan MD
Nida N. Ahmed MD
Zunirah Ahmed MD
Allan Seibert MD
author_sort Syed M. Hasan MD
title Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
title_short Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
title_full Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
title_fullStr Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
title_full_unstemmed Response of Bortezomib Chemotherapy in Hepatic Amyloidosis
title_sort response of bortezomib chemotherapy in hepatic amyloidosis
publisher SAGE Publishing
series Journal of Investigative Medicine High Impact Case Reports
issn 2324-7096
publishDate 2018-03-01
description Amyloidosis is a rare disorder with a wide spectrum of presentations and anomalies. It is subdivided into 2 broad categories based on protein deposition; primary and secondary amyloidosis. It can present as a single-organ involvement or as a diffuse infiltrative multi-organ process. Isolated hepatic amyloidosis presentation is a rare phenomenon that develops due to insoluble amyloid deposition in liver. Its clinical presentation is usually vague and ranges from mild hepatomegaly with elevated liver enzymes to acute liver failure and hepatic rupture. Currently, there are scarce data available regarding treatment options for biopsy-proven hepatic amyloidosis. In this review article, we present an interesting case of hepatic amyloidosis and its poor outcome to new molecular targeted chemotherapy. Furthermore, we aim to review current and future diagnostic tools for early detection and advancements in targeted chemotherapeutics options available for hepatic amyloidosis.
url https://doi.org/10.1177/2324709618760079
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