𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Emergency liver transplantation for hereditary lysozyme amyloidosis

✍ Scribed by George FG Mells; John AC Buckels; Douglas Thorburn


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
42 KB
Volume
12
Category
Article
ISSN
1527-6465

No coin nor oath required. For personal study only.


πŸ“œ SIMILAR VOLUMES


Hereditary lysozyme amyloidosis: Spontan
✍ Martin Loss; Wa S. Ng; Rooshdiya Z. Karim; Simone I. Strasser; David J. Koorey; πŸ“‚ Article πŸ“… 2006 πŸ› John Wiley and Sons 🌐 English βš– 254 KB

Hepatic rupture is a rare condition, and treatment options are very limited. We report a case of hepatic rupture secondary to hereditary lysozyme amyloidosis that was successfully treated by liver transplantation. The mother of this patient had presented in an identical fashion 15 years earlier in t

Long-term outcomes of emergency liver tr
✍ Gabriel Chan; Ali Taqi; Paul Marotta; Mark Levstik; Vivian McAlister; William Wa πŸ“‚ Article πŸ“… 2009 πŸ› John Wiley and Sons 🌐 English βš– 107 KB

Acute liver failure continues to be associated with a high mortality rate, and emergency liver transplantation is often the only life-saving treatment. The short-term outcomes are decidedly worse in comparison with those for nonurgent cases, whereas the long-term results have not been reported as ex

Gene therapy: Lessons learned from liver
✍ Ole B. Suhr; GΓΆsta Holmgren; Erik Lundgren πŸ“‚ Article πŸ“… 2004 πŸ› John Wiley and Sons 🌐 English βš– 75 KB

Familial amyloidotic polyneuropathy is the common form of hereditary generalized amyloidosis and is characterized by the accumulation of amyloid fibrils in the peripheral nerves and other organs. Liver transplantation (LTx) has been utilized as a therapy for familial amyloidotic polyneuropathy becau

Bevacizumab reverses need for liver tran
✍ Andrew Mitchell; Leon A. Adams; Gerry MacQuillan; Jon Tibballs; Rohan vanden Dri πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 153 KB

Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease characterized by mucocutaneous and visceral telangiectasia. Hepatic involvement with vascular malformations may lead to portal hypertension, biliary ischemia, and high-output cardiac failure. Liver transplantation is indica

Reply: Bevacizumab reverses need for liv
✍ Leon A. Adams; Andrew Mitchell; Gerry MacQuillan; Jonathon Tibballs; Rohan vande πŸ“‚ Article πŸ“… 2008 πŸ› John Wiley and Sons 🌐 English βš– 61 KB

unclear, and further experience in a clinical trial setting is required to clarify this. Lastly, it is exciting to ponder that vascular endothelial growth factor antagonists may have a role in reducing symptoms in the substantial number of HHT patients who are symptomatic but do not require liver tr

Liver transplantation for cardiac failur
✍ Thierry Thevenot; Claire Vanlemmens; Vincent Di Martino; Marie-Claude Becker; Pi πŸ“‚ Article πŸ“… 2005 πŸ› John Wiley and Sons 🌐 English βš– 96 KB

Liver involvement in hereditary hemorrhagic telangiectasia may lead to high-output cardiac failure. Few data have been reported on orthotopic liver transplantation (OLT) for these patients. In this paper, we describe two patients treated by OLT as a salvage procedure for cardiac failure, and we revi