非典型桡骨纵向缺损的长期随访：病例报告。

IF 1.3 4区医学 Q3 PEDIATRICS

Congenital Anomalies Pub Date : 2024-04-25 DOI:10.1111/cga.12570

Hiroshi Satake, Ryuji Takeuchi, Yasushi Naganuma, Toshiya Nito, Naomi Hanaka, Junichiro Shibuya, Masahiro Maruyama, Ryusuke Honma, Michiaki Takagi

{"title":"非典型桡骨纵向缺损的长期随访：病例报告。","authors":"Hiroshi Satake, Ryuji Takeuchi, Yasushi Naganuma, Toshiya Nito, Naomi Hanaka, Junichiro Shibuya, Masahiro Maruyama, Ryusuke Honma, Michiaki Takagi","doi":"10.1111/cga.12570","DOIUrl":null,"url":null,"abstract":"<p>We experienced an atypical case of radial longitudinal deficiency that did not fit into any classifications, including Blauth. The patient had a bilateral hypoplastic thumb, in which the index and middle fingers were missing in the right hand. We performed surgeries in four stages: centralization of the right hand, opponensplasty of the right thumb, opponensplasty of the left thumb, and distraction lengthening of the right ulnar. Twenty-five years after the initial treatment, the patient was satisfied with the treatment and had no significant difficulty with activities of daily living.</p>","PeriodicalId":10626,"journal":{"name":"Congenital Anomalies","volume":null,"pages":null},"PeriodicalIF":1.3000,"publicationDate":"2024-04-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Long-term follow-up for the atypical radial longitudinal deficiency: A case report\",\"authors\":\"Hiroshi Satake, Ryuji Takeuchi, Yasushi Naganuma, Toshiya Nito, Naomi Hanaka, Junichiro Shibuya, Masahiro Maruyama, Ryusuke Honma, Michiaki Takagi\",\"doi\":\"10.1111/cga.12570\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>We experienced an atypical case of radial longitudinal deficiency that did not fit into any classifications, including Blauth. The patient had a bilateral hypoplastic thumb, in which the index and middle fingers were missing in the right hand. We performed surgeries in four stages: centralization of the right hand, opponensplasty of the right thumb, opponensplasty of the left thumb, and distraction lengthening of the right ulnar. Twenty-five years after the initial treatment, the patient was satisfied with the treatment and had no significant difficulty with activities of daily living.</p>\",\"PeriodicalId\":10626,\"journal\":{\"name\":\"Congenital Anomalies\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":1.3000,\"publicationDate\":\"2024-04-25\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Congenital Anomalies\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/cga.12570\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"PEDIATRICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Congenital Anomalies","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/cga.12570","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"PEDIATRICS","Score":null,"Total":0}

引用次数: 0

摘要

我们遇到过一个非典型的桡骨纵向缺损病例，它不符合包括布劳特在内的任何分类。患者有双侧拇指发育不良，右手食指和中指缺失。我们分四个阶段进行了手术：右手集中手术、右手拇指对侧成形术、左手拇指对侧成形术和右手尺骨牵引延长术。初次治疗 25 年后，患者对治疗效果表示满意，日常生活没有明显困难。

本文章由计算机程序翻译，如有差异，请以英文原文为准。

查看原文本刊更多论文

Long-term follow-up for the atypical radial longitudinal deficiency: A case report

We experienced an atypical case of radial longitudinal deficiency that did not fit into any classifications, including Blauth. The patient had a bilateral hypoplastic thumb, in which the index and middle fingers were missing in the right hand. We performed surgeries in four stages: centralization of the right hand, opponensplasty of the right thumb, opponensplasty of the left thumb, and distraction lengthening of the right ulnar. Twenty-five years after the initial treatment, the patient was satisfied with the treatment and had no significant difficulty with activities of daily living.

求助全文

通过发布文献求助，成功后即可免费获取论文全文。去求助

来源期刊

Congenital Anomalies PEDIATRICS-

自引率

0.00%

发文量

审稿时长

>12 weeks

期刊介绍： Congenital Anomalies is the official English language journal of the Japanese Teratology Society, and publishes original articles in laboratory as well as clinical research in all areas of abnormal development and related fields, from all over the world. Although contributions by members of the teratology societies affiliated with The International Federation of Teratology Societies are given priority, contributions from non-members are welcomed.