Literature DB >> 12839296

Reversibility of cirrhotic regenerative liver nodules upon NTBC treatment in a child with tyrosinaemia type I.

J Crone1, D Möslinger, O A Bodamer, W Schima, W D Huber, E Holme, S Stöckler Ipsiroglu.   

Abstract

UNLABELLED: In a male patient with hereditary tyrosinaemia type I (HTI), NTBC [2-(2-nitro-4-trifluoro-methylbenzoyl)-1,3-cyclohexandion] treatment and a diet low in phenylalanine and tyrosine were started at the age of 4 wk. At the recommended average dosage (1 mg kg(-1)), liver failure improved transiently. After 4 mo of treatment, with increased body weight, the dose had decreased to 0.7 mg kg(-1), and diffuse cirrhotic changes in liver parenchyma and multiple nodules were visualized by ultrasonography. Multiple nodules in the liver parenchyma were differentiated from hepatocellular carcinoma by magnetic resonance imaging (MRI) using mangafodipir trisodium as a paramagnetic liver-specific contrast agent. Augmentation of NTBC dosage resulted in a decrease in serum alpha-fetoprotein levels and in significant regression of liver nodules on MRI.
CONCLUSION: In HTI patients with a poor response to NTBC treatment and/or development of cirrhotic changes of liver parenchyma, augmentation of the recommended NTBC dosage may result in significant improvement of symptoms.

Entities:  

Mesh:

Substances:

Year:  2003        PMID: 12839296

Source DB:  PubMed          Journal:  Acta Paediatr        ISSN: 0803-5253            Impact factor:   2.299


  8 in total

1.  Hereditary tyrosinemia type 1 from a single center in Egypt: clinical study of 22 cases.

Authors:  Hanaa El-Karaksy; Mona Fahmy; Mona El-Raziky; Nehal El-Koofy; Rokaya El-Sayed; Mohamed S Rashed; Hasan El-Kiki; Ahmad El-Hennawy; Nabil Mohsen
Journal:  World J Pediatr       Date:  2011-06-01       Impact factor: 2.764

2.  Cas9-nickase-mediated genome editing corrects hereditary tyrosinemia in rats.

Authors:  Yanjiao Shao; Liren Wang; Nana Guo; Shengfei Wang; Lei Yang; Yajing Li; Mingsong Wang; Shuming Yin; Honghui Han; Li Zeng; Ludi Zhang; Lijian Hui; Qiurong Ding; Jiqin Zhang; Hongquan Geng; Mingyao Liu; Dali Li
Journal:  J Biol Chem       Date:  2018-03-05       Impact factor: 5.157

3.  Nitisinone in the treatment of hereditary tyrosinaemia type 1.

Authors:  Patrick J McKiernan
Journal:  Drugs       Date:  2006       Impact factor: 9.546

4.  Intensive care management of children with acute liver failure.

Authors:  Vidyut Bhatia; Rakesh Lodha
Journal:  Indian J Pediatr       Date:  2010-08-27       Impact factor: 1.967

5.  NTBC treatment in tyrosinaemia type I: long-term outcome in French patients.

Authors:  A Masurel-Paulet; J Poggi-Bach; M-O Rolland; O Bernard; N Guffon; D Dobbelaere; J Sarles; H Ogier de Baulny; G Touati
Journal:  J Inherit Metab Dis       Date:  2008-01-25       Impact factor: 4.982

Review 6.  Current strategies for the treatment of hereditary tyrosinemia type I.

Authors:  Merja Ashorn; Sari Pitkänen; Matti K Salo; Markku Heikinheimo
Journal:  Paediatr Drugs       Date:  2006       Impact factor: 3.022

Review 7.  Recommendations for the management of tyrosinaemia type 1.

Authors:  Corinne de Laet; Carlo Dionisi-Vici; James V Leonard; Patrick McKiernan; Grant Mitchell; Lidia Monti; Hélène Ogier de Baulny; Guillem Pintos-Morell; Ute Spiekerkötter
Journal:  Orphanet J Rare Dis       Date:  2013-01-11       Impact factor: 4.123

8.  Revisiting hereditary tyrosinemia Type 1-spectrum of radiological findings.

Authors:  Sana Shaikh; Asma Qureshi; Syed Mohammad Faiq
Journal:  BJR Case Rep       Date:  2018-11-07
  8 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.