Case Report: Rupture of a gastric varix in liver cirrhosis associated with glycogen storage disease type III

被引:4
作者
Hashimoto, M
Watanabe, G
Yokoyama, T
Tsutsumi, K
Dohi, T
Matsuda, M
Okubo, M
Nakamura, N
Tsurumaru, M
机构
[1] Toranomon Gen Hosp, Dept Digest Surg, Minato Ku, Tokyo 105, Japan
[2] Toranomon Gen Hosp, Dept Endocrinol & Metab, Tokyo, Japan
[3] Univ Tsukuba, Dept Pediat, Ibaragi, Japan
关键词
debranching enzyme deficiency; glycogen storage disease type III; Hassab's operation; liver cirrhosis; oesophagogastric varix; portal hypertension;
D O I
10.1111/j.1440-1746.1998.tb00643.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Glycogen storage disease type III, or Cori's disease, is caused by a deficiency of amylo-1,6-glucosidase (debranching enzyme), which leads to the storage of an abnormal glycogen in the liver and in skeletal and heart muscle. Glycogen storage disease type III is usually characterized by hepatic symptoms, growth failure and myopathy. Even though liver cirrhosis is reported, portal hypertension is a rare complication of this disease. We describe the ease of a glycogen storage disease type III patient who was diagnosed at 3 years of age and developed complications (liver cirrhosis and rupture of a gastric varix) at 31 gears of age. We discuss the histological progression to cirrhosis of the liver and describe the liver enzyme profile at 3 and 31 years of age.
引用
收藏
页码:232 / 235
页数:4
相关论文
共 50 条
  • [41] Prenatal diagnosis and carrier detection for glycogen storage disease type III using polymorphic DNA markers
    Shen, JJ
    Liu, HM
    McConkie-Rosell, A
    Chen, YT
    PRENATAL DIAGNOSIS, 1998, 18 (01) : 61 - 64
  • [42] The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type III
    Jing Wang
    Yuping Yu
    Chunquan Cai
    Xiufang Zhi
    Ying Zhang
    Yu Zhao
    Jianbo Shu
    BMC Pediatrics, 22
  • [43] Whole-Body Muscle Magnetic Resonance Imaging in Glycogen-Storage Disease Type III
    Tobaly, David
    Laforet, Pascal
    Perry, Ariane
    Habes, Dalila
    Labrune, Philippe
    Decostre, Valerie
    Masingue, Marion
    Petit, Francois
    Barp, Andrea
    Bello, Luca
    Carlier, Pierre
    Carlier, Robert-Yves
    MUSCLE & NERVE, 2019, 60 (01) : 72 - 79
  • [44] The biallelic novel pathogenic variants in AGL gene in a chinese patient with glycogen storage disease type III
    Wang, Jing
    Yu, Yuping
    Cai, Chunquan
    Zhi, Xiufang
    Zhang, Ying
    Zhao, Yu
    Shu, Jianbo
    BMC PEDIATRICS, 2022, 22 (01)
  • [45] Liver cirrhosis and splenomegaly associated with Schistosoma mansoni in a Sudanese woman in Malaysia:A case report
    Yamuna Rajoo
    Rohela Mahmud
    Ng Rong Xiang
    Sharifah F.S.Omar
    G Kumar
    Yvonne A.L Lim
    Arine Fadzlun Ahmad
    Amirah Amir
    Zurainee Mohamed Nor
    Romano Ngui
    Asian Pacific Journal of Tropical Medicine, 2015, (04) : 334 - 336
  • [46] Spontaneous Rupture of the Internal Thoracic Artery Causing a Mediastinal Hematoma in a Patient with Alcoholic Liver Cirrhosis: A Case Report
    Park, Jae Yang
    Kang, Eun-Ju
    Park, Jaehyung
    JOURNAL OF THE KOREAN SOCIETY OF RADIOLOGY, 2023, 84 (03): : 750 - 756
  • [47] Liver cirrhosis and splenomegaly associated with Schistosoma mansoni in a Sudanese woman in Malaysia: A case report
    Rajoo, Yamuna
    Mahmud, Rohela
    Xiang, Ng Rong
    Omar, Sharifah F. S.
    Kumar, G.
    Lim, Yvonne A. L.
    Ahmad, Arine Fadzlun
    Amir, Amirah
    Nor, Zurainee Mohamed
    Ngui, Romano
    ASIAN PACIFIC JOURNAL OF TROPICAL MEDICINE, 2015, 8 (04) : 334 - 336
  • [48] Mutational analysis of ten Turkish patients with glycogen storage disease type III: identification of four novel mutations
    Manguoglu, Esra
    Uygun, Vedat
    Ozkaya, Figen
    Luleci, Guven
    Artan, Reha
    Berker, Sibel
    TURK PEDIATRI ARSIVI-TURKISH ARCHIVES OF PEDIATRICS, 2012, 47 (04): : 278 - 282
  • [49] Genotype-phenotype correlation in two frequent mutations and mutation update in type III glycogen storage disease
    Shaiu, WL
    Kishnani, PS
    Shen, JJ
    Liu, HM
    Chen, YT
    MOLECULAR GENETICS AND METABOLISM, 2000, 69 (01) : 16 - 23
  • [50] A lower energetic, protein and uncooked cornstarch intake is associated with a more severe outcome in glycogen storage disease type III: an observational study of 50 patients
    Ben Chehida, Amel
    Ben Messaoud, Sana
    Ben Abdelaziz, Rim
    Mansouri, Hajer
    Boudabous, Hela
    Hakim, Kaouthar
    Ben Ali, Nadia
    Ben Ameur, Zeineb
    Sassi, Yosra
    Kaabachi, Neziha
    Abdelhak, Sonia
    Abdelmoula, Mohamed Slim
    Azzouz, Hatem
    Tebib, Neji
    JOURNAL OF PEDIATRIC ENDOCRINOLOGY & METABOLISM, 2018, 31 (09) : 979 - 986