• 徐州醫(yī)學(xué)院附屬醫(yī)院普外科(江蘇徐州 221002);

1 臨床資料  患者,女,27歲,因左上腹疼痛不適1月入院。腹痛呈持續(xù)性隱痛,伴腹脹。無(wú)鼻衄、嘔血及黑便史,無(wú)關(guān)節(jié)疼痛及癲癇發(fā)作史。 其姐姐因戈謝病行脾切除術(shù),病情穩(wěn)定已8年余。 查體: 一般情況可,鞏膜無(wú)黃斑,心肺無(wú)異常。腹稍膨隆,左上腹輕壓痛,肝肋下約5 cm,脾肋下約10 cm,脾下極達(dá)盆腔,肝、脾無(wú)壓痛……

引用本文: 張蓬波,郭萌,任澤強(qiáng),張秀忠. 成人型戈謝病1例報(bào)道并文獻(xiàn)復(fù)習(xí). 中國(guó)普外基礎(chǔ)與臨床雜志, 2009, 16(12): 1048-1049. doi: 復(fù)制

1. Jmoudiak M, Futerman AH. Gaucher disease:pathological mechanisms and modern management [J]. Br J Haematol, 2005; 129(2): 178-188.
2. 施惠平, 張為民, 臧晏, 等. 中國(guó)10例戈謝病基因型與臨床表型的相關(guān)性 [J]. 中華兒科雜志, 2001; 39(3): 131-133.
3. Stirnemann J, Caubel I, Kettaneh A, et al. Epidemiologic, clinical, biological and therapeutic aspects of Gaucher disease [J]. Presse Med, 2003; 32(11): 503-511.
4. 李金, 汪海源, 邵華, 等. 戈謝病的研究進(jìn)展 [J]. 國(guó)外醫(yī)學(xué)兒科學(xué)分冊(cè), 2002; 29(5): 274-276.
5. 張宗利, 高延超, 鄭立杰. 成人型戈謝病2例 [J]. 中國(guó)實(shí)用外科雜志, 2008; 28(7): 599-600.
6. 段彥龍, 張永紅, 臧晏, 等. 酶替代治療戈謝病72例 [J]. 中華兒科雜志, 2006; 44(9): 653-656.
7. Weinreb NJ, Charrow J, Andersson HC, et al. Effectiveness of enzyme replacement therapy in 1 028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry [J]. Am J Med, 2002; 113(2): 112-119.
8. Goldblatt J, Szer J, Fletcher JM, et al. Enzyme replacement therapy for Gaucher disease in Australia [J]. Intern Med J, 2005; 35(3): 156-161.
9. Rozé B, Lambert Y, Potard M, et al. Voluminous nodular splenomegaly in Gaucher disease: A case report [J]. Rev Med Interne, 2009; 30(10): 904-906.
10. Pastores GM, Barnett NL, Kolodny EH. An open-ladel, noncomparative study of miglustat in typeⅠGaucher disease: efficacy and tolerability over 24 months of treatment [J]. Clin Ther, 2005; 27(8): 1215-1227.
  1. 1. Jmoudiak M, Futerman AH. Gaucher disease:pathological mechanisms and modern management [J]. Br J Haematol, 2005; 129(2): 178-188.
  2. 2. 施惠平, 張為民, 臧晏, 等. 中國(guó)10例戈謝病基因型與臨床表型的相關(guān)性 [J]. 中華兒科雜志, 2001; 39(3): 131-133.
  3. 3. Stirnemann J, Caubel I, Kettaneh A, et al. Epidemiologic, clinical, biological and therapeutic aspects of Gaucher disease [J]. Presse Med, 2003; 32(11): 503-511.
  4. 4. 李金, 汪海源, 邵華, 等. 戈謝病的研究進(jìn)展 [J]. 國(guó)外醫(yī)學(xué)兒科學(xué)分冊(cè), 2002; 29(5): 274-276.
  5. 5. 張宗利, 高延超, 鄭立杰. 成人型戈謝病2例 [J]. 中國(guó)實(shí)用外科雜志, 2008; 28(7): 599-600.
  6. 6. 段彥龍, 張永紅, 臧晏, 等. 酶替代治療戈謝病72例 [J]. 中華兒科雜志, 2006; 44(9): 653-656.
  7. 7. Weinreb NJ, Charrow J, Andersson HC, et al. Effectiveness of enzyme replacement therapy in 1 028 patients with type 1 Gaucher disease after 2 to 5 years of treatment: a report from the Gaucher Registry [J]. Am J Med, 2002; 113(2): 112-119.
  8. 8. Goldblatt J, Szer J, Fletcher JM, et al. Enzyme replacement therapy for Gaucher disease in Australia [J]. Intern Med J, 2005; 35(3): 156-161.
  9. 9. Rozé B, Lambert Y, Potard M, et al. Voluminous nodular splenomegaly in Gaucher disease: A case report [J]. Rev Med Interne, 2009; 30(10): 904-906.
  10. 10. Pastores GM, Barnett NL, Kolodny EH. An open-ladel, noncomparative study of miglustat in typeⅠGaucher disease: efficacy and tolerability over 24 months of treatment [J]. Clin Ther, 2005; 27(8): 1215-1227.