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相似文献

1
Immune deficiency, thrombocytopenia and osteomyelitis in pediatric patients.儿科患者的免疫缺陷、血小板减少症和骨髓炎
Yale J Biol Med. 1978 Jul-Aug;51(4):435-40.
2
[Metabolic defect of thrombocytopenic thrombocytopathia in the Wiskott-Aldrich syndrome (author's transl)].
Nihon Ketsueki Gakkai Zasshi. 1975 Dec;38(6):786-92.
3
[A case of Wiskott-Aldrich syndrome with specific immunological deficiencies].一例伴有特异性免疫缺陷的维斯科特-奥尔德里奇综合征
Pediatria (Napoli). 1976 Mar 31;84(1):110-9.
4
[Early surgical intervention in acute hematogenic osteomyelitis of the long tubular bones in children].
Vestn Khir Im I I Grek. 1979 Dec;123(12):83-5.
5
Rituximab for the treatment of autoimmune cytopenias in children with immune deficiency.利妥昔单抗用于治疗免疫缺陷儿童的自身免疫性血细胞减少症。
Br J Haematol. 2007 Jul;138(1):94-6. doi: 10.1111/j.1365-2141.2007.06616.x. Epub 2007 May 11.
6
Pseudo-osteomyelitis in Gaucher's disease.
Orthop Rev. 1989 Aug;18(8):880-8.
7
Cutaneous manifestations of immunogenetic deficiency disorders.免疫遗传学缺陷疾病的皮肤表现
Birth Defects Orig Artic Ser. 1981;17(2):93-115.
8
Hypercatabolism of IgG, IgA, IgM, and albumin in the Wiskott-Aldrich syndrome. A unique disorder of serum protein metabolism.威斯科特-奥尔德里奇综合征中IgG、IgA、IgM和白蛋白的高分解代谢。一种血清蛋白代谢的独特紊乱。
J Clin Invest. 1971 Nov;50(11):2331-8. doi: 10.1172/JCI106731.
9
[The Wiskott-Aldrich syndrome with verrucae vulgares].
Hautarzt. 1977 Dec;28(12):664-7.
10
Pyogenic osteomyelitis versus pseudo-osteomyelitis in Gaucher's disease. Report of a case and review of the literature.
Clin Pediatr (Phila). 1981 Oct;20(10):667-9. doi: 10.1177/000992288102001009.

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Skeletal manifestations and treatment of Gaucher's disease. Review of twenty cases.
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Gaucher's disease: pathogenetic considerations based on electron microscopic and histochemical observations.戈谢病:基于电子显微镜和组织化学观察的发病机制思考
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Acute hematogenous osteomyelitis. A review of sixty-six cases.急性血源性骨髓炎。66例病例回顾。
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Disturbed epiphysial growth at the knee after osteomyelitis in infancy.婴儿期骨髓炎后膝关节骨骺生长紊乱。
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Management of common bacterial infections of bones and joints.
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Wiskott Aldrich syndrome: a treatable immune disorder. A review.威斯科特-奥尔德里奇综合征:一种可治疗的免疫紊乱。综述。
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儿科患者的免疫缺陷、血小板减少症和骨髓炎

Immune deficiency, thrombocytopenia and osteomyelitis in pediatric patients.

作者信息

Clark C R, Lee K E, Ogden J A, McIntosh L S

出版信息

Yale J Biol Med. 1978 Jul-Aug;51(4):435-40.

PMID:751324
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2595619/
Abstract

Surgical decompression of osteomyelitis in pediatric patients should be an essential part of therapy in most cases. The initial deferral of prompt decompression in two patients because of underlying chronic, hemorrhagic (thrombocytopenic) disorders-one with Wiskott-Aldrich syndrome and one with Gaucher's disease-resulted in more serious and prolonged courses of the infectious processes. The complications might have been ameliorated by earlier drainage in each case. Based upon the experience gained from these two patients, we recommend early drainage, with appropriate treatment of the hemorrhagic disorder, to prevent more widespread dissemination or prolongation of osseous infection in similarly affected children.

摘要

在大多数情况下,小儿骨髓炎的手术减压应是治疗的重要组成部分。两名患者因潜在的慢性出血性(血小板减少性)疾病——一名患有维斯科特-奥尔德里奇综合征,另一名患有戈谢病——而最初推迟了及时减压,这导致感染过程更加严重和漫长。在每种情况下,早期引流可能会减轻并发症。基于从这两名患者身上获得的经验,我们建议早期引流,并对出血性疾病进行适当治疗,以防止在类似受影响的儿童中骨感染更广泛地扩散或延长。