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组织细胞增多症X的生存质量:西南肿瘤学组研究

Quality of survival in histiocytosis X: a Southwest Oncology Group study.

作者信息

Komp D M, El Mahdi A, Starling K A, Easley J, Vietti T J, Berry D H, George S L

出版信息

Med Pediatr Oncol. 1980;8(1):35-40. doi: 10.1002/mpo.2950080106.

DOI:10.1002/mpo.2950080106
PMID:6969347
Abstract

Sixty children survived for five years after the diagnosis of histiocytosis X. Serious disabilities were seen in 50% of children whose disease involved soft tissue and bone. Late deaths from pulmonary failure were associated with opportunistic infections in two cases. Future treatment approaches must weigh the risks of therapy-related complications against the probability of significant disability if the disease continues for many years.

摘要

60名儿童在被诊断为勒-雪病后存活了5年。在疾病累及软组织和骨骼的儿童中,50%出现了严重残疾。两例因呼吸衰竭导致的晚期死亡与机会性感染有关。未来的治疗方法必须权衡治疗相关并发症的风险与如果疾病持续多年出现严重残疾的可能性。

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Quality of survival in histiocytosis X: a Southwest Oncology Group study.组织细胞增多症X的生存质量:西南肿瘤学组研究
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J Cutan Pathol. 2011 Mar;38(3):280-5. doi: 10.1111/j.1600-0560.2010.01650.x. Epub 2010 Dec 12.
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Treatment of Langerhans cell histiocytosis--evolution and current approaches.朗格汉斯细胞组织细胞增多症的治疗——进展与当前方法
Br J Cancer Suppl. 1994 Sep;23:S41-6.
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Langerhans cell histiocytosis--clinical and epidemiological aspects.朗格汉斯细胞组织细胞增多症——临床与流行病学方面
Br J Cancer Suppl. 1994 Sep;23:S11-6.
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Progressive spinocerebellar degeneration "plus" associated with Langerhans cell histiocytosis: a new paraneoplastic syndrome?与朗格汉斯细胞组织细胞增多症相关的进行性脊髓小脑变性“加征”:一种新的副肿瘤综合征?
J Neurol Neurosurg Psychiatry. 1995 Feb;58(2):180-3. doi: 10.1136/jnnp.58.2.180.
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Histiocytosis X--current controversies.组织细胞增多症X——当前的争议
Arch Dis Child. 1985 Jul;60(7):605-7. doi: 10.1136/adc.60.7.605.
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Favourable prognostic features in histiocytosis X: bone involvement and absence of skin disease.组织细胞增多症X的良好预后特征:骨骼受累及无皮肤疾病。
Arch Dis Child. 1986 Dec;61(12):1219-21. doi: 10.1136/adc.61.12.1219.