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病例报告:21 世纪罕见的跛行原因。

Case Report: Uncommon cause of limp in the 21 century.

机构信息

Department of Women, Children, and Adolescents, Service of General Pediatrics, Geneva University Hospitals, Geneva, Switzerland.

Unit of Development and Research in Medical Education, University of Geneva Faculty of Medicine, Geneva, Switzerland.

出版信息

Front Endocrinol (Lausanne). 2022 Aug 1;13:968015. doi: 10.3389/fendo.2022.968015. eCollection 2022.

DOI:10.3389/fendo.2022.968015
PMID:35979442
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9377508/
Abstract

Scurvy results from a deficiency of ascorbic acid. This disease first appeared in children during the 19th century with the emergence of new dietary habits; in particular, heating milk that leads to a loss of ascorbic acid. Even though scurvy has become a rare condition in western countries, many cases are still reported in pediatric patients, especially in those who lack proper nutrition due to neurological or psychiatric illnesses. Symptoms include bleeding and swollen gums, loosening of teeth, bone abnormalities, arthralgia, delayed wound healing, anemia, petechiae, and purpura. Bone lesions are mainly irregularities of long bones metaphyses. We report the case of a five-year-old boy who presented with arthralgia and limb deformation (genu valgum). The patient was investigated for vitamin deficiencies to exclude rickets. The radiologic investigations revealed metaphyseal signs compatible with scurvy. During the hospitalization, the patient was observed to have abnormal eating patterns and the scurvy was attributed to malnutrition. Although the occurrence of scurvy is rare, it remains essential to detect this disease in children at risk of developing vitamin deficiencies. Without targeted treatment, the complications of scurvy can be serious and potentially fatal.

摘要

坏血病是由于抗坏血酸缺乏引起的。这种疾病在 19 世纪随着新的饮食习惯的出现首次出现在儿童中;特别是加热牛奶会导致抗坏血酸的损失。尽管坏血病在西方国家已很少见,但仍有许多儿科患者报告病例,特别是在因神经或精神疾病而缺乏适当营养的患者中。症状包括出血和肿胀的牙龈、牙齿松动、骨骼异常、关节痛、伤口愈合延迟、贫血、瘀点和紫癜。骨骼病变主要是长骨干骺端的不规则。我们报告了一例五岁男孩的病例,他出现了关节痛和肢体变形(膝外翻)。为排除佝偻病,对患者进行了维生素缺乏检查。放射学检查显示符合坏血病的干骺端征象。在住院期间,观察到患者有异常的饮食习惯,坏血病归因于营养不良。尽管坏血病的发生率较低,但仍有必要检测有发生维生素缺乏风险的儿童的这种疾病。如果不进行针对性治疗,坏血病的并发症可能很严重,甚至可能致命。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/0ed51dc1a548/fendo-13-968015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/c6b2ec834b2a/fendo-13-968015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/c8d24d6bfff9/fendo-13-968015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/66423685df1e/fendo-13-968015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/0ed51dc1a548/fendo-13-968015-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/c6b2ec834b2a/fendo-13-968015-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/c8d24d6bfff9/fendo-13-968015-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/66423685df1e/fendo-13-968015-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/fa34/9377508/0ed51dc1a548/fendo-13-968015-g004.jpg

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本文引用的文献

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Modern Day Scurvy in Pediatric Orthopaedics: A Forgotten Illness.现代小儿矫形外科坏血病:一种被遗忘的疾病。
J Pediatr Orthop. 2021 Mar 1;41(3):e279-e284. doi: 10.1097/BPO.0000000000001731.
3
Scurvy in pediatric age group - A disease often forgotten?小儿年龄组中的坏血病——一种常被遗忘的疾病?
BMJ Case Rep. 2023 Dec 30;16(12):e258819. doi: 10.1136/bcr-2023-258819.
4
Scurvy in a young man: a rare case report.一名年轻男性的坏血病:罕见病例报告
Front Nutr. 2023 Oct 17;10:1265334. doi: 10.3389/fnut.2023.1265334. eCollection 2023.
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Scurvy: Rediscovering a Forgotten Disease.坏血病:重新发现一种被遗忘的疾病。
Diseases. 2023 May 26;11(2):78. doi: 10.3390/diseases11020078.
J Clin Orthop Trauma. 2015 Jun;6(2):101-7. doi: 10.1016/j.jcot.2014.12.003. Epub 2015 Jan 5.
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MRI findings in pediatric patients with scurvy.患坏血病儿科患者的磁共振成像结果
Skeletal Radiol. 2015 Feb;44(2):291-7. doi: 10.1007/s00256-014-1962-y. Epub 2014 Aug 12.
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Serum vitamin C and the prevalence of vitamin C deficiency in the United States: 2003-2004 National Health and Nutrition Examination Survey (NHANES).血清维生素 C 与美国维生素 C 缺乏症的流行情况:2003-2004 年全国健康和营养调查(NHANES)。
Am J Clin Nutr. 2009 Nov;90(5):1252-63. doi: 10.3945/ajcn.2008.27016. Epub 2009 Aug 12.
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