Bégány A, Nagy-Vezekényi K, Nagy E, Zeher M
Klinik für Dermatologie und Venerologie, Universitat Debrecen, Ungarn.
Z Hautkr. 1989 Mar 15;64(3):228-30.
We report on a 19-year-old girl with hepatosplenomegaly and possible hematological disease. We suspected Gaucher's disease on account of histological and biochemical evidence found in specimens from the liver, spleen, and bone marrow. 18 months later, pebbled skin developed on her neck and upper back. Histological examination revealed large amounts of mucous material between the collagen bundles deep in the dermis, which proved to be dermatan sulfate. The clinical and histological symptoms are characteristic for Hunter's disease.
我们报告了一名19岁患有肝脾肿大及可能患有血液系统疾病的女孩。基于在肝脏、脾脏和骨髓标本中发现的组织学和生化证据,我们怀疑她患有戈谢病。18个月后,她的颈部和上背部出现了鹅卵石样皮肤。组织学检查显示真皮深层胶原束之间有大量黏液物质,经证实为硫酸皮肤素。这些临床和组织学症状是亨特氏病的特征。