Two simultaneous anatomical variations of the cervical spine - a case report discussing the concept of tandem anomalies.

IF 1.2 4区 医学 Q3 ANATOMY & MORPHOLOGY
Joanna Jaworek-Troć, Izabela Zamojska, Michał Zarzecki, Bartosz Kołodziejczyk, Jerzy Andrzej Walocha, Jarosław Zawiliński, Marcin Lipski, Przemysław Pękala
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引用次数: 0

Abstract

forming a bony opening through which the vertebral artery (VA) enters the vertebral canal. Block vertebra is a synostosis of at least two vertebral bodies that did not separate during the embryological development. It is worth distinguishing it from the Klippel-Feil syndrome, as the latter oftentimes involves other abnormalities (namely skeletal) and is typically diagnosed in childhood. Both variants could potentially lead to an impairment of the blood flow through the VA. Case report: The following case report presents a finding of two anomalies of the cervical spine, found in a 38 y.o. female patient suffering from dizziness. A synostosis of the C4 and C5 vertebral bodies, arches and zygapophysial (facet) joint, was noted by the examining radiologist, with marked narrowing of the intervertebral foramen. Furthermore, second anatomical variation in the form of the complete bilateral arcuate foramen was identified superior to the groove for the VA on the upper surface of the posterior arch of the atlas. Conclusions: To the best knowledge of the authors, this case report is the first to present a co-existing block vertebra and bilateral complete arcuate foramen. Common presence of at least two anatomical variations that could have a synergistic clinical effect could possibly be termed 'tandem anomaly.' Notwithstanding, identification of a single anomaly explaining a patient's symptoms does not absolve the medical professionals from searching for any other potential variations that could also be present and could further influence the clinical picture.

颈椎同时出现两种解剖变异--讨论串联异常概念的病例报告。
形成一个骨性开口,椎动脉(VA)通过该开口进入椎管。阻滞椎是至少两个在胚胎发育过程中没有分离的椎体的合体。值得将其与克利珀尔-费尔综合征(Klippel-Feil Syndrome)区分开来,因为后者通常涉及其他畸形(即骨骼畸形),并且通常在儿童时期诊断出来。这两种变异都可能导致通过 VA 的血流受损。病例报告:下面的病例报告介绍了一名 38 岁女性头晕患者的颈椎两处异常。放射科医生检查发现,C4 和 C5 椎体、椎弓和颧骨关节(面关节)突合,椎间孔明显变窄。此外,在寰椎后弓上表面的VA凹槽上方,还发现了第二种解剖变异,即完整的双侧弓状孔。结论据作者所知,本病例报告是第一例同时存在阻滞椎和双侧完整弓状孔的病例。至少两种解剖变异的共同存在可能会产生协同的临床效应,这可能会被称为 "串联异常"。尽管如此,医学专家在发现单一异常可解释患者的症状时,并不能免除寻找其他潜在变异的责任,这些变异也可能存在,并可能进一步影响临床表现。
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来源期刊
Folia morphologica
Folia morphologica ANATOMY & MORPHOLOGY-
CiteScore
2.40
自引率
0.00%
发文量
218
审稿时长
6-12 weeks
期刊介绍: "Folia Morphologica" is an official journal of the Polish Anatomical Society (a Constituent Member of European Federation for Experimental Morphology - EFEM). It contains original articles and reviews on morphology in the broadest sense (descriptive, experimental, and methodological). Papers dealing with practical application of morphological research to clinical problems may also be considered. Full-length papers as well as short research notes can be submitted. Descriptive papers dealing with non-mammals, cannot be accepted for publication with some exception.
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