Literature DB >> 22227073

Progressive mesenteric lymphadenopathy with protein-losing enteropathy; a devastating complication in Gaucher disease.

Beom Hee Lee1, Dae-Yeon Kim, Gu-Hwan Kim, Kyung-Ja Cho, Hye-Kyung Yoon, Han-Wook Yoo.   

Abstract

Mesenteric lymphadenopathy has been rarely reported in pediatric patients with Gaucher disease, developing despite the enzyme replacement therapy. The clinical implication of this condition is undetermined, with no consensus on treatment strategies. However, this condition can reflect the progression of Gaucher disease. Moreover, it can be accompanied by the serious complication, protein-losing enteropathy. Our experience underlines the importance of careful monitoring and early intervention for mesenteric lymphadenopathy, especially in pediatric patients with neuronopathic Gaucher disease. Copyright Â
© 2011 Elsevier Inc. All rights reserved.

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Year:  2011        PMID: 22227073     DOI: 10.1016/j.ymgme.2011.12.010

Source DB:  PubMed          Journal:  Mol Genet Metab        ISSN: 1096-7192            Impact factor:   4.797


  8 in total

1.  Allele frequency of a 24 bp duplication in exon 10 of the CHIT1 gene in the general Korean population and in Korean patients with Gaucher disease.

Authors:  Kyu Ha Woo; Beom Hee Lee; Sun Hee Heo; Jae-Min Kim; Gu-Hwan Kim; Yoo-Mi Kim; Ja Hye Kim; In-Hee Choi; Song Hyun Yang; Han-Wook Yoo
Journal:  J Hum Genet       Date:  2014-03-13       Impact factor: 3.172

2.  Safety and efficacy of eliglustat combined to enzyme replacement therapy for lymphadenopathy in patients with Gaucher disease type 3.

Authors:  Ni-Chung Lee; Yin-Hsiu Chien; Chung-Hsing Wang; Siew-Lee Wong; Steven Shinn-Forng Peng; Fuu-Jen Tsai; Wuh-Liang Hwu
Journal:  Mol Genet Metab Rep       Date:  2022-04-19

Review 3.  Cervical lymph node diseases in children.

Authors:  Stephan Lang; Benjamin Kansy
Journal:  GMS Curr Top Otorhinolaryngol Head Neck Surg       Date:  2014-12-01

4.  Gaucher Disease with Mesenteric Lymphadenopathy: A Case with 13-year Follow-up.

Authors:  Zi-Xing Ye; Xiang Gao; Qiang Qu; Xin Ye; Xiao-Dong He
Journal:  Chin Med J (Engl)       Date:  2016-10-20       Impact factor: 2.628

5.  Successful therapy for protein-losing enteropathy caused by chronic neuronopathic Gaucher disease.

Authors:  A A Mhanni; M Kozenko; J N Hartley; M Deneau; W El-Matary; C Rockman-Greenberg
Journal:  Mol Genet Metab Rep       Date:  2015-12-29

6.  Case report of unexpected gastrointestinal involvement in type 1 Gaucher disease: comparison of eliglustat tartrate treatment and enzyme replacement therapy.

Authors:  Yoo-Mi Kim; Dong Hoon Shin; Su Bum Park; Chong Kun Cheon; Han-Wook Yoo
Journal:  BMC Med Genet       Date:  2017-05-15       Impact factor: 2.103

7.  Very rare condition of multiple Gaucheroma: A case report and review of the literature.

Authors:  Szu-Yin Tseng; Dau-Ming Niu; Tzu-Hung Chu; Yi-Chen Yeh; Man-Hsu Huang; Tsui-Feng Yang; Hsuan-Chieh Liao; Chuan-Chi Chiang; Hui-Chen Ho; Wen-Jue Soong; Chia-Feng Yang
Journal:  Mol Genet Metab Rep       Date:  2019-05-09

8.  Very rare condition of multiple Gaucheroma: A case report and review of the literature.

Authors:  Szu-Yin Tseng; Dau-Ming Niu; Tzu-Hung Chu; Yi-Chen Yeh; Man-Hsu Huang; Tsui-Feng Yang; Hsuan-Chieh Liao; Chuan-Chi Chiang; Hui-Chen Ho; Wen-Jue Soong; Chia-Feng Yang
Journal:  Mol Genet Metab Rep       Date:  2019-07-12
  8 in total

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