Polymelia of the upper limb

Q4 Medicine
Sergey I. Golyana
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 CLINICAL CASE: A 2-year-old child diagnosed with polymelia of the right upper limb was examined and treated at our clinic. Clinical examination revealed two shoulder blades and one clavicle, with a normal anatomical location and development. Behind, an upper limb ended with the stump of the forearm, represented by an underdeveloped ulna. Moreover, the elbow joint was in a state of flexion contracture at an angle of 170, and the ulna was turned posteriorly and 1520 medially. The anterior humerus in the proximal section was underdeveloped, and in the distal section, it articulated in a normally formed elbow joint with the radius and ulna. The hand had five fingers with moderate underdevelopment and deformity of the 5th finger. After examining the bone, muscle, and vascular anatomy of the doubled limb, surgery was performed; as a result, a nearly complete anatomical and functional limb was reconstructed from the two segments of one upper limb.
 DISCUSSION: Polymelia is an extremely rare variant of a congenital anomaly of the limbs; thus, only a few cases are reported in the literature, which differs significantly from each other in clinical manifestations. Many questions related to the etiology and pathogenesis of these malformations are unexplored. The doubling of the limbs in animals is caused by both teratogenic environmental factors and genetic mutations. In any case, reconstructive surgery makes it possible to effectively treat children with such anomalies in the development of the limbs and obtain good results.
 CONCLUSIONS: The restoration of the upper limb of children with polymelia is quite difficult, but doable. Adequate analysis of all examination data and rational planning of surgical intervention in such cases creates conditions that enable achieving the maximum anatomical and functional results of upper limb reconstruction in children with this developmental anomaly.","PeriodicalId":37631,"journal":{"name":"Pediatric Traumatology, Orthopaedics and Reconstructive Surgery","volume":"14 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2023-10-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Pediatric Traumatology, Orthopaedics and Reconstructive Surgery","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.17816/ptors492255","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0

Abstract

BACKGROUND: The most rare and extremely rare malformation of the upper limb is polymelia, i.e., doubling (triple) limb. In the literature, no more than 20 cases of an increase in the number of lower limbs and only three cases of doubling (triple) of the upper limb (in humans) have been described. CLINICAL CASE: A 2-year-old child diagnosed with polymelia of the right upper limb was examined and treated at our clinic. Clinical examination revealed two shoulder blades and one clavicle, with a normal anatomical location and development. Behind, an upper limb ended with the stump of the forearm, represented by an underdeveloped ulna. Moreover, the elbow joint was in a state of flexion contracture at an angle of 170, and the ulna was turned posteriorly and 1520 medially. The anterior humerus in the proximal section was underdeveloped, and in the distal section, it articulated in a normally formed elbow joint with the radius and ulna. The hand had five fingers with moderate underdevelopment and deformity of the 5th finger. After examining the bone, muscle, and vascular anatomy of the doubled limb, surgery was performed; as a result, a nearly complete anatomical and functional limb was reconstructed from the two segments of one upper limb. DISCUSSION: Polymelia is an extremely rare variant of a congenital anomaly of the limbs; thus, only a few cases are reported in the literature, which differs significantly from each other in clinical manifestations. Many questions related to the etiology and pathogenesis of these malformations are unexplored. The doubling of the limbs in animals is caused by both teratogenic environmental factors and genetic mutations. In any case, reconstructive surgery makes it possible to effectively treat children with such anomalies in the development of the limbs and obtain good results. CONCLUSIONS: The restoration of the upper limb of children with polymelia is quite difficult, but doable. Adequate analysis of all examination data and rational planning of surgical intervention in such cases creates conditions that enable achieving the maximum anatomical and functional results of upper limb reconstruction in children with this developmental anomaly.
上肢多肢症
背景:上肢最罕见和极其罕见的畸形是多肢畸形,即双肢(三肢)。在文献中,下肢数量增加的病例不超过20例,上肢(人类)增加一倍(三倍)的病例只有3例。 临床病例:一名2岁儿童被诊断为右上肢多裂,在我诊所接受检查和治疗。临床检查发现两个肩胛骨和一个锁骨,解剖位置和发育正常。在后面,上肢以前臂的残肢结束,以未发育的尺骨为代表。肘关节处于170角屈曲挛缩状态,尺骨向后转动,向内侧转动1520角。肱骨前段近段发育不全,远段与桡骨、尺骨形成正常肘关节。手部有五个手指,第五个手指发育不全,畸形。在检查了双肢的骨骼、肌肉和血管解剖后,进行手术;结果,从一个上肢的两个节段重建了一个几乎完整的解剖和功能肢体。 讨论:多肢畸形是一种极其罕见的四肢先天性异常的变体;因此,文献中仅报道了少数病例,其临床表现差异较大。许多与这些畸形的病因和发病机制有关的问题尚未得到探讨。动物四肢的加倍是由致畸环境因素和基因突变共同引起的。无论如何,重建手术可以有效地治疗这种肢体发育异常的儿童,并获得良好的效果。 结论:多足症患儿上肢的修复是相当困难的,但也是可行的。充分分析所有检查数据,合理规划手术干预,为这种发育异常的儿童上肢重建创造条件,使其获得最大的解剖和功能效果。
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来源期刊
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery
Pediatric Traumatology, Orthopaedics and Reconstructive Surgery Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.50
自引率
0.00%
发文量
38
期刊介绍: The target audience of the journal is researches, physicians, orthopedic trauma, burn, and pediatric surgeons, anesthesiologists, pediatricians, neurologists, oral surgeons, and all specialists in related fields of medicine.
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