Pre-splenectomy permanent tooth extraction in a child with hereditary spherocytosis: a case report and guidelines care.

IF 1.5 4区 医学 Q3 DENTISTRY, ORAL SURGERY & MEDICINE
Journal of Clinical Pediatric Dentistry Pub Date : 2024-11-01 Epub Date: 2024-11-03 DOI:10.22514/jocpd.2024.143
Patrick Pereira Garcia, Luenny Maria Moraes Pinheiro, Wellington José Alves Nunes, Rudys Rodolfo de Jesus Tavares, Cyrene Piazera Silva Costa
{"title":"Pre-splenectomy permanent tooth extraction in a child with hereditary spherocytosis: a case report and guidelines care.","authors":"Patrick Pereira Garcia, Luenny Maria Moraes Pinheiro, Wellington José Alves Nunes, Rudys Rodolfo de Jesus Tavares, Cyrene Piazera Silva Costa","doi":"10.22514/jocpd.2024.143","DOIUrl":null,"url":null,"abstract":"<p><p>Hereditary Spherocytosis (HS) is a type of hemolytic anemia characterized by a defect in the membrane of red blood cells, which causes them to assume a spherical shape, become osmotically fragile, and be prone to early hemolysis. While it is relatively well understood in the medical field, there is limited evidence regarding the dental management of patients with this condition. Therefore, this report aims to present a case involving the extraction of permanent teeth before splenectomy in a child with HS who had been hospitalized. Additionally, treatment guidelines for these patients are proposed and developed. The patient was scheduled to undergo a total splenectomy due to splenomegaly resulting from severe hemolytic anemia. Prior to the surgery, the child was referred to the hospital's dental clinic with a chief complaint of dental pain. An intraoral examination revealed carious lesions with pulpal involvement in the first molars, and extraction was recommended to minimize the risk of post-splenectomy infection. Hematological support was provided during dental treatment since partial control of the anemia was necessary for the extraction procedure. Developing dental treatment guidelines for patients with HS is essential to ensure their safety.</p>","PeriodicalId":50235,"journal":{"name":"Journal of Clinical Pediatric Dentistry","volume":"48 6","pages":"221-224"},"PeriodicalIF":1.5000,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Clinical Pediatric Dentistry","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.22514/jocpd.2024.143","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/11/3 0:00:00","PubModel":"Epub","JCR":"Q3","JCRName":"DENTISTRY, ORAL SURGERY & MEDICINE","Score":null,"Total":0}
引用次数: 0

Abstract

Hereditary Spherocytosis (HS) is a type of hemolytic anemia characterized by a defect in the membrane of red blood cells, which causes them to assume a spherical shape, become osmotically fragile, and be prone to early hemolysis. While it is relatively well understood in the medical field, there is limited evidence regarding the dental management of patients with this condition. Therefore, this report aims to present a case involving the extraction of permanent teeth before splenectomy in a child with HS who had been hospitalized. Additionally, treatment guidelines for these patients are proposed and developed. The patient was scheduled to undergo a total splenectomy due to splenomegaly resulting from severe hemolytic anemia. Prior to the surgery, the child was referred to the hospital's dental clinic with a chief complaint of dental pain. An intraoral examination revealed carious lesions with pulpal involvement in the first molars, and extraction was recommended to minimize the risk of post-splenectomy infection. Hematological support was provided during dental treatment since partial control of the anemia was necessary for the extraction procedure. Developing dental treatment guidelines for patients with HS is essential to ensure their safety.

遗传性球形红细胞增多症患儿脾切除术前恒牙拔除:病例报告和护理指南。
遗传性球形红细胞增多症(HS)是一种溶血性贫血,其特点是红细胞膜存在缺陷,导致红细胞呈球形,渗透性脆弱,容易发生早期溶血。虽然医学界对这种疾病的了解相对较多,但有关牙科治疗这种疾病的证据却很有限。因此,本报告旨在介绍一例在脾切除术前拔除恒牙的 HS 住院患儿。此外,还提出并制定了针对此类患者的治疗指南。患者因严重溶血性贫血导致脾脏肿大而被安排接受全脾切除术。手术前,患儿被转诊到医院的牙科诊所,主诉为牙齿疼痛。口腔内检查发现第一磨牙有牙髓受累的龋齿病变,建议拔除以尽量减少脾切除术后感染的风险。由于需要部分控制贫血才能进行拔牙手术,因此在牙科治疗期间提供了血液支持。为恒河猴患者制定牙科治疗指南对于确保他们的安全至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Journal of Clinical Pediatric Dentistry
Journal of Clinical Pediatric Dentistry DENTISTRY, ORAL SURGERY & MEDICINE-PEDIATRICS
CiteScore
1.80
自引率
7.70%
发文量
47
期刊介绍: The purpose of The Journal of Clinical Pediatric Dentistry is to provide clinically relevant information to enable the practicing dentist to have access to the state of the art in pediatric dentistry. From prevention, to information, to the management of different problems encountered in children''s related medical and dental problems, this peer-reviewed journal keeps you abreast of the latest news and developments related to pediatric dentistry.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信