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一例罕见的进行性系统性硬化症病例,发病于儿童早期,继发于传染性单核细胞增多症。

Unusual case of progressive systemic sclerosis with onset in early childhood and following infectious mononucleosis.

作者信息

Urano J, Kohno H, Watanabe T

出版信息

Eur J Pediatr. 1981 Jul;136(3):285-9. doi: 10.1007/BF00442996.

DOI:10.1007/BF00442996
PMID:6973466
Abstract

A rare case of infantile progressive systemic sclerosis is reported. A Japanese girl suffered from infectious mononucleosis at the age of 1 year 3 months, and 5 months later she developed edema and sclerosis of the skin. She has been followed up for 4 years and now has grotesque features, with contractures of hands and feet due to advanced systemic sclerosis. The relationship between infectious mononucleosis and progressive systemic sclerosis is discussed.

摘要

报告了一例罕见的婴儿进行性系统性硬化症病例。一名日本女孩在1岁3个月时患传染性单核细胞增多症,5个月后出现皮肤水肿和硬化。她已接受随访4年,目前因晚期系统性硬化症而出现面容怪异,伴有手足挛缩。文中讨论了传染性单核细胞增多症与进行性系统性硬化症之间的关系。

相似文献

1
Unusual case of progressive systemic sclerosis with onset in early childhood and following infectious mononucleosis.一例罕见的进行性系统性硬化症病例,发病于儿童早期,继发于传染性单核细胞增多症。
Eur J Pediatr. 1981 Jul;136(3):285-9. doi: 10.1007/BF00442996.
2
[Disorders of cellular immunity in systemic scleroderma].[系统性硬化症中的细胞免疫紊乱]
Przegl Lek. 1988;45(7):592-7.
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Pathogenesis of progressive systemic sclerosis.进行性系统性硬化症的发病机制。
Int J Dermatol. 1986 Jun;25(5):286-93. doi: 10.1111/j.1365-4362.1986.tb02244.x.
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T and B lymphocytes in peripheral blood of children with infectious mononucleosis and tonsillitis.传染性单核细胞增多症和扁桃体炎患儿外周血中的T淋巴细胞和B淋巴细胞。
Acta Paediatr Acad Sci Hung. 1980;21(1):27-31.
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Letter: Immunologic sequelae of infectious mononucleosis.信件:传染性单核细胞增多症的免疫后遗症
N Engl J Med. 1975 Sep 25;293(13):668. doi: 10.1056/NEJM197509252931319.
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[T- and B-lymphocyte determination in infectious mononucleosis].[传染性单核细胞增多症中T淋巴细胞和B淋巴细胞的测定]
Fortschr Med. 1977 Jun 16;95(23):1506-8.
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A brief overview of the pathogenesis of scleroderma (systemic sclerosis).硬皮病(系统性硬化症)发病机制简述。
Ann Rheum Dis. 1992 Feb;51(2):286-8. doi: 10.1136/ard.51.2.286.
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Infectious mononucleosis and the Epstein-Barr virus.传染性单核细胞增多症与爱泼斯坦-巴尔病毒
Am J Dis Child. 1978 Jan;132(1):78-86. doi: 10.1001/archpedi.1978.02120260080020.
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[Immunological cell surface markers in infectious mononucleosis (author's transl)].传染性单核细胞增多症中的免疫细胞表面标志物(作者译)
Klin Wochenschr. 1976 Jul 1;54(13):647-8. doi: 10.1007/BF01469032.
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Is agranulocytosis following infectious mononucleosis caused by autoimmunity?传染性单核细胞增多症后的粒细胞缺乏症是由自身免疫引起的吗?
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Virus-Induced MicroRNA Modulation and Systemic Sclerosis Disease.病毒诱导的微小RNA调控与系统性硬化症
Biomedicines. 2024 Jun 19;12(6):1360. doi: 10.3390/biomedicines12061360.
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Infections are not increased in scleroderma compared to non-inflammatory musculoskeletal disorders prior to disease onset.与疾病发作前的非炎性肌肉骨骼疾病相比,硬皮病患者的感染情况并未增加。
Open Rheumatol J. 2007;1:12-7. doi: 10.2174/1874312900701010012. Epub 2007 Nov 8.

本文引用的文献

1
ANTINUCLEAR AND PRECIPITATING AUTOANTIBODIES IN PROGRESSIVE SYSTEMIC SCLEROSIS.进行性系统性硬化症中的抗核抗体和沉淀性自身抗体
Lancet. 1963 Dec 7;2(7319):1188-90.
2
Generalized scleroderma in children. Acrosclerotic type.儿童全身性硬皮病。肢端硬化型。
Arch Dermatol. 1961 Mar;83:402-13. doi: 10.1001/archderm.1961.01580090052005.
3
Systemic scleroderma, A clinical study of 727 cases.系统性硬化症:727例临床研究
Arch Dermatol. 1961 Sep;84:359-71. doi: 10.1001/archderm.1961.01580150005001.
4
Calcinosis cutis: its relationship to scleroderma.皮肤钙质沉着症:其与硬皮病的关系。
AMA Arch Derm. 1959 Jul;80(1):15-21. doi: 10.1001/archderm.1959.01560190017002.
5
Epidemiology of systemic sclerosis (scleroderma).系统性硬化症(硬皮病)的流行病学
Ann Intern Med. 1971 May;74(5):714-21. doi: 10.7326/0003-4819-74-5-714.
6
Progressive systemic sclerosis. Diagnosis at the age of 4 years.进行性系统性硬化症。4岁时确诊。
Am J Dis Child. 1972 Jan;123(1):57-60.
7
Scleroderma in the child.儿童硬皮病
J Pediatr. 1974 Dec;85(6):770-5. doi: 10.1016/s0022-3476(74)80338-0.
8
Scleroderma in childhood.儿童硬皮病
Ann Rheum Dis. 1976 Jun;35(3):189-97. doi: 10.1136/ard.35.3.189.
9
Scleroderma: pathogenic factors and current management.硬皮病:致病因素与当前治疗方法
Aust N Z J Med. 1978;8 Suppl 1:143-8. doi: 10.1111/j.1445-5994.1978.tb04809.x.
10
Scleroderma.硬皮病
Med Clin North Am. 1977 Mar;61(2):283-97. doi: 10.1016/s0025-7125(16)31333-5.