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Ultrasound evaluation of the femoral trochlea in newborns: incidence of trochlear dysplasia and associated risk factors. 新生儿股骨滑车的超声评估:滑车发育不良的发生率及相关危险因素。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2023-10-31 DOI: 10.1097/BPB.0000000000001141
Javier Masquijo, Angeles Bruno, Agustina Warde, Carola Mónico, Florencia Turazza

This study aimed to describe the femoral groove morphology using ultrasound in children under 6 months, estimate the incidence of trochlear dysplasia, and evaluate associated risk factors. A prospective study included 298 patients who underwent universal ultrasound screening for hip dysplasia [developmental dysplasia of the hip (DDH)] and knee ultrasound. Measurements of sulcus angle (SA), trochlear depth (TD), and trochlear facet asymmetry (TFA) were analyzed. Trochlear dysplasia was considered present if the ASO was ≥159°. Reproducibility was assessed using the intraclass correlation coefficient (ICC) in 60 knees. Logistic regression adjusted for confounders, presenting odds ratios (OR) and 95% confidence intervals (CI). Significance was set at P  < 0.05. Analysis included 596 knees (298 patients). Females accounted for 51% of patients, with 7% having breech presentation, 4.4% DDH, 6.4% family history of DDH, and 5% family history of patellofemoral instability. ICC showed excellent agreement for SA and TD, but poor for TFA. Trochlear dysplasia incidence was 3% (9/298; 67% bilateral). Median (IQR) values were 147.5 (144.0-150.5) for SA, 2.4 (2.2-2.8) for TD, and 1.1 (1.0, 1.1) for TFA. Breech presentation (OR, 9.68; 95% CI 1.92-48.71, P  = 0.006) and concomitant DDH (OR 6.29, 95% CI 1.04-37.78, P  = 0.044) were associated with trochlear dysplasia. Ultrasound effectively evaluates femoral groove morphology and diagnoses trochlear dysplasia in newborns. Trochlear dysplasia incidence was 3%, with a 10-fold higher risk in breech presentation and 6-fold higher risk in concomitant DDH. Standardized screening and timely treatment protocols should be further investigated. Level of evidence: Diagnostic Level II.

本研究旨在用超声描述6个月以下儿童的股沟形态,估计滑车发育不良的发生率,并评估相关的危险因素。一项前瞻性研究包括298名接受髋关节发育不良(DDH)和膝关节超声检查的患者。分析了滑车沟角(SA)、滑车深度(TD)和滑车小面不对称性(TFA)的测量结果。如果ASO≥159°,则认为存在Trochlear发育不良。使用组内相关系数(ICC)对60个膝关节的再现性进行评估。Logistic回归对混杂因素进行了调整,呈现优势比(OR)和95%置信区间(CI)。显著性设置为P
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引用次数: 0
Evaluation of posterior tibial slope relationship with common knee pathologies in pediatric and adolescent age groups in the Turkish population. 评估土耳其儿童和青少年群体中胫骨后斜坡与常见膝关节病变的关系。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-02-19 DOI: 10.1097/BPB.0000000000001171
Haluk Yaka, Onur Bilge, Ahmet Fevzi Kekeç, Mehmet Demiryürek, Mahmut Nedim Doral

Anterior cruciate ligament rupture (ACLR), tibial eminence fracture (TEF), and Osgood-Schlatter disease (OSD) have been linked to a steep posterior tibial slope (PTS) in children and adolescents. This study aims to examine and compare these associations. 418 patients aged 8-18, 237 males and 181 females with knee pain between 2010 and 2019 were included and the patients belonged to the Turkish population. They consisted of ACLR (n = 47), TEF (n = 22), OSD (n = 51), and a control group (n = 298). The study and control groups were compared for PTS, sex, and age, with ACLR, TEF, OSD, retrospectively. The ACLR, OSD, and TEF groups had higher PTS values than the control group ( P < 0.001). There was no significant difference in ACLR-OSD, ACLR-TEF, and OSD-TEF comparisons ( P = 0.22, P = 0.99, and P = 0.99, respectively). PTS increase was linked to ACLR, TEF, and OSD in the multinomial regression analysis, ( P < 0.001). Increase in PTS was associated with ACLR, TEF, and OSD for both males and females (independently of other factors; ACLR: P < 0.001, P < 0.001, OR: 1.59, OR: 2.63, TEF: P = 0.001, P < 0.001, OR: 1.98, OR: 1.44; OSD: P = 0.001, P < 0.001, OR: 1.49, OR: 1.28 for males and females respectively). ACLR, TEF, and OSD are associated with increased PTS in the pediatric and adolescent age groups, and there are differences between these pathologies in terms of the amount of PTS increase, age, and sex. Consideration of age and gender in pediatric and adolescent patients with increased PTS may be useful in predicting pathologies associated with increased PTS. Level of evidence: III retrospective comparative study.

在儿童和青少年中,前交叉韧带断裂(ACLR)、胫骨突骨折(TEF)和奥斯古德-施拉特病(OSD)与胫骨后斜坡(PTS)陡峭有关。本研究旨在检查和比较这些关联。研究纳入了 418 名年龄在 8-18 岁之间、在 2010 年至 2019 年期间患有膝关节疼痛的患者,其中男性 237 人,女性 181 人。其中包括 ACLR 组(n = 47)、TEF 组(n = 22)、OSD 组(n = 51)和对照组(n = 298)。研究组和对照组在 PTS、性别和年龄方面进行了比较,并对 ACLR、TEF 和 OSD 进行了回顾性分析。ACLR、OSD 和 TEF 组的 PTS 值高于对照组(P < 0.001)。ACLR-OSD 组、ACLR-TEF 组和 OSD-TEF 组的比较无明显差异(分别为 P = 0.22、P = 0.99 和 P = 0.99)。在多项式回归分析中,PTS 的增加与 ACLR、TEF 和 OSD 相关(P < 0.001)。男性和女性的 PTS 增加与 ACLR、TEF 和 OSD 相关(与其他因素无关;ACLR:P < 0.001,P < 0.001,OR:1.59,OR:2.63,TEF:P = 0.001,P = 0.99):P=0.001,P<0.001,OR:1.98,OR:1.44;OSD:P=0.001,P<0.001,OR:1.49,男性和女性的OR:1.28)。在儿童和青少年年龄组中,ACLR、TEF 和 OSD 与 PTS 增加有关,而且这些病症在 PTS 增加的程度、年龄和性别方面存在差异。考虑PTS增加的儿童和青少年患者的年龄和性别可能有助于预测与PTS增加相关的病理情况。证据等级:III 级回顾性比较研究。
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引用次数: 0
Should I stay or should I go: an assessment of criteria for safe day of surgery discharge of displaced supracondylar humerus fractures. 该留还是该走:对肱骨髁上移位骨折手术当天安全出院标准的评估。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI: 10.1097/BPB.0000000000001191
Andreas Rehm, Nicholas Judkins, Silvester Kabwama, Sebastian Ho, Ayla C Newton, Elizabeth Ashby
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引用次数: 0
Outcomes of late-stages infantile Blount's disease managed by acute single stage: medial hemi-plateau elevation and metaphyseal osteotomy. Eight case series. 急性单期治疗晚期婴儿布朗特病的结果:内侧半平台抬高和干骺端截骨术。八个案例系列。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2023-11-16 DOI: 10.1097/BPB.0000000000001143
Vidyasagar Chandankere, Maryada Venkateshwarlu Reddy, Annapareddy Venkata Gurava Reddy

This study aimed to evaluate the clinical and radiological outcomes of surgical intervention involving acute medial hemi-plateau elevation and metaphyseal osteotomy with internal fixation and growth modulation for late-stages Blount's disease. A retrospective analysis was conducted on consecutive patients with late-stages infantile tibia vara between 2014 and 2020. Inclusion criteria consisted of children aged 8 years and older with Blount's disease with Langenskiold stage IV, V or VI, tibia vara more than 30*, medial plateau depression angle (MPDA) exceeding 25* and knee instability with a minimum follow-up period of 3 years. Patients with Limb length discrepancy greater than 5 cm were excluded. Data collection included assessments of age, weight, disease stage, clinical tibiofemoral angle (TFA), mechanical medial proximal tibial angle (mMPTA), MPDA, tibial torsion and knee instability. Functional outcomes were evaluated using modified Pediatric Outcome Data Collection Instruments (PODCI) scores. The study included 5 children with 8 affected limbs. Among them, three children with five limbs had recurrent deformities after previous surgeries. All cases showed significant improvements in TFAs, mMPTA, tibial torsion, knee instability and modified PODCI scores. Complications included 4 cases of superficial infections, 1 intra-articular fracture, 2 minor screw breakage and 2 on-table under correction. Surgical intervention involving acute Single-stage medial hemi-plateau elevation and metaphyseal osteotomy leads to satisfactory outcomes in late-stages Blount's disease among older children. It is crucial to achieve proper correction of all deformity components during surgery, with epiphysiodesis on the lateral side to prevent further recurrence. Continuous follow-up until skeletal maturity is essential for optimal results.

本研究旨在评估急性内侧半平台抬高和干骺端截骨内固定和生长调节手术治疗晚期布朗特病的临床和影像学结果。回顾性分析2014 - 2020年间连续发生的晚期婴儿胫骨内翻患者。纳入标准为年龄在8岁及以上的布朗特病Langenskiold期IV、V或VI期患儿,胫骨内翻大于30*,内侧平台凹陷角(MPDA)超过25*,膝关节不稳定,随访时间至少为3年。排除肢体长度差异大于5 cm的患者。数据收集包括评估年龄、体重、疾病分期、临床胫股角(TFA)、机械胫骨内侧近端角(mMPTA)、MPDA、胫骨扭转和膝关节不稳定。使用改进的儿科结局数据收集工具(PODCI)评分评估功能结局。该研究包括5名儿童,8个患肢。其中,有3名五肢儿童在既往手术后出现复发性畸形。所有病例在tfa、mMPTA、胫骨扭转、膝关节不稳定和改良PODCI评分方面均有显著改善。并发症包括4例浅表感染,1例关节内骨折,2例轻微螺钉断裂,2例矫正手术台上。手术干预包括急性单期中期半平台抬高和干骺端截骨术,可导致大龄儿童晚期布朗特病的满意结果。在手术中实现所有畸形组成部分的适当矫正是至关重要的,外侧的表皮成形术可以防止进一步复发。为了获得最佳效果,持续随访直到骨骼成熟。
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引用次数: 0
'Six years of experience with the nationwide newborn ultrasonographic hip screening program in Turkey: a considerable change in the type of surgical interventions in developmental dysplasia of the hip'. 土耳其全国新生儿髋关节超声波筛查计划的六年经验:髋关节发育不良的手术干预类型发生了巨大变化"。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI: 10.1097/BPB.0000000000001199
Rashid Anjum
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引用次数: 0
Lower limb coronal malalignment correction by percutaneous osteotomy and schanz screws fixation. 通过经皮截骨术和Schanz螺钉固定矫正下肢冠状位错位。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-02-26 DOI: 10.1097/BPB.0000000000001176
Khaled Mohamed Emara, Ramy Ahmed Diab, Mohamed N Essa, Mohamed Eissa, Mahmoud Ahmed Elshobaky, Ahmed K Emara, Kyrillos Rashid, Mahmoud Abuelwafa, Mostafa Gemeah

Pediatric knee deformities are common, and the classic treatment is corrective osteotomy. The aim of this study to assess the safety and efficacy of percutaneous low-energy osteotomy and casting with shanz screws fixation in treatment of Genu varum in children equal or younger than 7 years. This is a prospective nonrandomized case series study was conducted. A total of 38 patients (total of 60 limbs: 36 varus and 24 valgus) were treated by percutaneous low-energy osteotomy and casting with shanz screws fixation and observed over 2-5 years. Clinical and radiological outcomes were evaluated at the end of follow-up period by standing scanogram which enabled tibiofemoral angles and the mechanical axis to be measured and the rate of complications. There was a statistically significant improvement of the radiographic parameters in the form of tibiofemoral angle and MAD. Clinically, all the cases were completely corrected just one patient (two limbs) complicated by over-correction but statically non-significant and. pin tract infection in shanz screws fixation was noticed in one Patient. Percutaneous low-energy osteotomy and casting with shanz screws fixation is a simple, safe, and effective method in dealing with 7 years and younger children with pathological knee deformities. Level of evidence: Therapeutic level IV.

小儿膝关节畸形很常见,经典的治疗方法是矫正截骨术。本研究的目的是评估经皮低能量截骨术和shanz螺钉固定铸造法治疗小于或等于7岁儿童膝关节外翻的安全性和有效性。这是一项前瞻性非随机病例系列研究。共有 38 名患者(共 60 个肢体:36 个外翻和 24 个内翻)接受了经皮低能量截骨术和山字形螺钉固定石膏治疗,并进行了 2-5 年的观察。在随访期结束时,通过立位扫描图对临床和放射学结果进行评估,从而测量胫骨与股骨的角度和机械轴以及并发症的发生率。从统计学角度看,胫骨与股骨的夹角和MAD的放射学参数都有明显改善。在临床上,所有病例都得到了完全矫正,只有一名患者(两只肢体)出现了过度矫正的并发症,但在统计学上并不明显。经皮低能量截骨术和shanz螺钉固定铸造术是治疗7岁及以下儿童病理性膝关节畸形的一种简单、安全、有效的方法。证据等级:治疗级别 IV。
{"title":"Lower limb coronal malalignment correction by percutaneous osteotomy and schanz screws fixation.","authors":"Khaled Mohamed Emara, Ramy Ahmed Diab, Mohamed N Essa, Mohamed Eissa, Mahmoud Ahmed Elshobaky, Ahmed K Emara, Kyrillos Rashid, Mahmoud Abuelwafa, Mostafa Gemeah","doi":"10.1097/BPB.0000000000001176","DOIUrl":"10.1097/BPB.0000000000001176","url":null,"abstract":"<p><p>Pediatric knee deformities are common, and the classic treatment is corrective osteotomy. The aim of this study to assess the safety and efficacy of percutaneous low-energy osteotomy and casting with shanz screws fixation in treatment of Genu varum in children equal or younger than 7 years. This is a prospective nonrandomized case series study was conducted. A total of 38 patients (total of 60 limbs: 36 varus and 24 valgus) were treated by percutaneous low-energy osteotomy and casting with shanz screws fixation and observed over 2-5 years. Clinical and radiological outcomes were evaluated at the end of follow-up period by standing scanogram which enabled tibiofemoral angles and the mechanical axis to be measured and the rate of complications. There was a statistically significant improvement of the radiographic parameters in the form of tibiofemoral angle and MAD. Clinically, all the cases were completely corrected just one patient (two limbs) complicated by over-correction but statically non-significant and. pin tract infection in shanz screws fixation was noticed in one Patient. Percutaneous low-energy osteotomy and casting with shanz screws fixation is a simple, safe, and effective method in dealing with 7 years and younger children with pathological knee deformities. Level of evidence: Therapeutic level IV.</p>","PeriodicalId":50092,"journal":{"name":"Journal of Pediatric Orthopaedics-Part B","volume":" ","pages":"552-559"},"PeriodicalIF":0.9,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140061113","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Conservative versus surgical treatment of Gartland type II supracondylar humeral fractures in children. 儿童加特兰德 II 型肱骨髁上骨折的保守治疗与手术治疗。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-02-19 DOI: 10.1097/BPB.0000000000001170
Danjiang Zhu, Yuwei Wen, Qiang Wang, Baojian Son, Wei Feng

The purpose of the study was to compare the efficacy of conservative and surgical treatments for Gartland type II supracondylar humerus fractures in children. We assessed 142 patients with type II supracondylar humerus fractures treated in our hospital from February 2018 to February 2019. The patients were divided into two groups: initial conservative treatment (Group A) and initial surgical treatment (Group B). Clinical outcomes were measured by the Flynn scoring system. Variables were analyzed using a statistical approach between those groups. All patients were followed up for 6-12 months. The rate of loss reduction was 19.8% in patients treated conservatively, and the incidence of pin infections was 7.1% in patients treated surgically. Although there were no statistical differences between the three groups in fracture healing time and Flynn score, the conservative treatment was superior to surgical treatment in functional recovery times. At the last follow-up, all fractures had healed without iatrogenic vascular or nerve injury, Volkmann's contracture, or cubit varus deformity. Conservative treatment is safe and effective for the treatment of Gartland type II supracondylar fracture and represents a faster recovery time of elbow range of motion as compared with surgical treatment. Type IIB had a 41.3% risk of secondary displacement versus 5.3% for IIA, but we still prefer closed reduction. However, closed reduction of Garland type II must be followed accurately in the first 2 weeks to identify patients with loss of reduction. The patients who loss reduction can be treated with percutaneous pinning, and the clinical effect was consistent with immediate surgical treatment. Level of evidence: level III.

本研究旨在比较儿童Gartland II型肱骨髁上骨折保守治疗和手术治疗的疗效。我们对2018年2月至2019年2月在我院接受治疗的142例II型肱骨髁上骨折患者进行了评估。患者分为两组:初始保守治疗组(A组)和初始手术治疗组(B组)。临床结果采用 Flynn 评分系统进行测量。采用统计学方法对两组之间的变量进行分析。所有患者均接受了 6-12 个月的随访。保守治疗患者的损失减少率为 19.8%,手术治疗患者的针脚感染发生率为 7.1%。虽然三组患者在骨折愈合时间和 Flynn 评分上没有统计学差异,但在功能恢复时间上,保守治疗优于手术治疗。在最后一次随访中,所有骨折均已愈合,没有出现先天性血管或神经损伤、沃尔克曼氏挛缩或立方体屈曲畸形。保守治疗对治疗 Gartland II 型肱骨髁上骨折安全有效,与手术治疗相比,肘关节活动范围恢复时间更快。IIB 型发生二次移位的风险为 41.3%,而 IIA 型为 5.3%,但我们仍倾向于采用闭合复位术。不过,Garland II 型闭合复位术必须在头两周内进行准确跟踪,以识别复位丧失的患者。对于复位丧失的患者,可以采用经皮固定治疗,其临床效果与立即手术治疗一致。证据等级:三级。
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引用次数: 0
Conservative versus surgical treatment of Gartland type II supracondylar humeral fractures in children. 儿童加特兰德 II 型肱骨髁上骨折的保守治疗与手术治疗。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI: 10.1097/BPB.0000000000001194
Andreas Rehm, Matthew Seah, Silvester Kabwama, Sebastian Ho, Ayla C Newton, Elizabeth Ashby
{"title":"Conservative versus surgical treatment of Gartland type II supracondylar humeral fractures in children.","authors":"Andreas Rehm, Matthew Seah, Silvester Kabwama, Sebastian Ho, Ayla C Newton, Elizabeth Ashby","doi":"10.1097/BPB.0000000000001194","DOIUrl":"10.1097/BPB.0000000000001194","url":null,"abstract":"","PeriodicalId":50092,"journal":{"name":"Journal of Pediatric Orthopaedics-Part B","volume":"33 6","pages":"607-608"},"PeriodicalIF":0.9,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142606381","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Should we rethink the approach to osteochondromas in dangerous anatomical sites in multiple hereditary exostoses? 我们是否应该重新考虑处理多发性遗传性骨软骨病危险解剖部位骨软骨瘤的方法?
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-11-01 Epub Date: 2024-10-01 DOI: 10.1097/BPB.0000000000001190
Nunzio Catena, Chiara Arrigoni, Valentina Camurri, Simone Riganti, Giorgio Marre' Brunenghi
{"title":"Should we rethink the approach to osteochondromas in dangerous anatomical sites in multiple hereditary exostoses?","authors":"Nunzio Catena, Chiara Arrigoni, Valentina Camurri, Simone Riganti, Giorgio Marre' Brunenghi","doi":"10.1097/BPB.0000000000001190","DOIUrl":"10.1097/BPB.0000000000001190","url":null,"abstract":"","PeriodicalId":50092,"journal":{"name":"Journal of Pediatric Orthopaedics-Part B","volume":"33 6","pages":"613-614"},"PeriodicalIF":0.9,"publicationDate":"2024-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142606426","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Dandy-Walker malformations with other complex congenital deformities associated with scoliosis: a case series. 丹迪-沃克畸形伴脊柱侧弯的其他复杂先天性畸形:病例系列。
IF 0.9 4区 医学 Q4 ORTHOPEDICS Pub Date : 2024-09-27 DOI: 10.1097/BPB.0000000000001213
Masayoshi Machida, Masafumi Machida, Katsuaki Taira, Naho Nemoto, Noboru Oikawa, Hirofumi Ohashi, Kazuyoshi Nakanishi

Dandy-Walker malformations (DWM) is a rare condition with an estimated prevalence of 1 in 30 000 cases. Although DWM often complicates scoliosis, its prevalence and the time of onset are unknown because only a few reports have described the association between scoliosis and DWM. This case series describes spinal deformity associated with DWM. The clinical records and spinal radiographs of 23 consecutive patients with DWM at a single centre were reviewed. DWM was clinically diagnosed if patients met the following three conditions: (1) posterior fossa enlargement, (2) cerebellar hypoplasia and (3) cystic dilation of the fourth ventricle on MRI. Radiological assessment records for the presence, prevalence and time of onset of DWM were studied. Twelve of 23 patients (52%) demonstrated a scoliotic deformity, with 3 (13%) having severe deformities exceeding 60°. The average age at diagnosis was 3.6 ± 2.9 years (range: 0.7-9.7) and at radiographic examination during the final follow-up was 8.7 years (range 1.0-22.0). Only two patients were skeletally mature. The coronal angular deformity at the final follow-up was 34.2 ± 32.3° (range: 10.1-125.1°). One patient with moderate deformity >25° died before bracing. In addition, of three patients with severe deformities, only one had undergone posterior spinal fusion. The prevalence of scoliosis in DWM was 52%, and all patients who developed scoliosis reported early-onset scoliosis under 10 years of age. Early diagnosis and screening of spine deformity are required for patients with DWM to prevent disease progression. Evidence level: 4.

丹迪-沃克畸形(Dandy-Walker malformations,DWM)是一种罕见疾病,发病率估计为1/30000。虽然DWM经常并发脊柱侧弯,但其发病率和发病时间尚不清楚,因为只有少数报道描述了脊柱侧弯与DWM之间的关联。本系列病例描述了与 DWM 相关的脊柱畸形。研究人员回顾了一个中心连续 23 例 DWM 患者的临床记录和脊柱X光片。如果患者符合以下三个条件,即可临床诊断为 DWM:(1) 后窝扩大;(2) 小脑发育不全;(3) 核磁共振成像显示第四脑室囊性扩张。研究人员对 DWM 的存在、发病率和发病时间进行了放射学评估记录。23名患者中有12人(52%)出现脊柱侧弯畸形,其中3人(13%)的严重畸形超过60°。确诊时的平均年龄为 3.6 ± 2.9 岁(范围:0.7-9.7 岁),最后随访期间接受放射学检查时的平均年龄为 8.7 岁(范围:1.0-22.0 岁)。只有两名患者骨骼发育成熟。最后随访时的冠状角畸形为 34.2 ± 32.3°(范围:10.1-125.1°)。一名中度畸形大于 25°的患者在支具安装前死亡。此外,在三名严重畸形的患者中,只有一人接受了脊柱后路融合术。DWM患者中脊柱侧弯的发病率为52%,所有出现脊柱侧弯的患者均在10岁以下早发。需要对DWM患者进行脊柱畸形的早期诊断和筛查,以防止疾病恶化。证据等级:4。
{"title":"Dandy-Walker malformations with other complex congenital deformities associated with scoliosis: a case series.","authors":"Masayoshi Machida, Masafumi Machida, Katsuaki Taira, Naho Nemoto, Noboru Oikawa, Hirofumi Ohashi, Kazuyoshi Nakanishi","doi":"10.1097/BPB.0000000000001213","DOIUrl":"https://doi.org/10.1097/BPB.0000000000001213","url":null,"abstract":"<p><p>Dandy-Walker malformations (DWM) is a rare condition with an estimated prevalence of 1 in 30 000 cases. Although DWM often complicates scoliosis, its prevalence and the time of onset are unknown because only a few reports have described the association between scoliosis and DWM. This case series describes spinal deformity associated with DWM. The clinical records and spinal radiographs of 23 consecutive patients with DWM at a single centre were reviewed. DWM was clinically diagnosed if patients met the following three conditions: (1) posterior fossa enlargement, (2) cerebellar hypoplasia and (3) cystic dilation of the fourth ventricle on MRI. Radiological assessment records for the presence, prevalence and time of onset of DWM were studied. Twelve of 23 patients (52%) demonstrated a scoliotic deformity, with 3 (13%) having severe deformities exceeding 60°. The average age at diagnosis was 3.6 ± 2.9 years (range: 0.7-9.7) and at radiographic examination during the final follow-up was 8.7 years (range 1.0-22.0). Only two patients were skeletally mature. The coronal angular deformity at the final follow-up was 34.2 ± 32.3° (range: 10.1-125.1°). One patient with moderate deformity >25° died before bracing. In addition, of three patients with severe deformities, only one had undergone posterior spinal fusion. The prevalence of scoliosis in DWM was 52%, and all patients who developed scoliosis reported early-onset scoliosis under 10 years of age. Early diagnosis and screening of spine deformity are required for patients with DWM to prevent disease progression. Evidence level: 4.</p>","PeriodicalId":50092,"journal":{"name":"Journal of Pediatric Orthopaedics-Part B","volume":" ","pages":""},"PeriodicalIF":0.9,"publicationDate":"2024-09-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142394766","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
期刊
Journal of Pediatric Orthopaedics-Part B
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