Bilateral asymmetrical variation of median artery in coexistence with bifid median nerve and variation in the origin and course of its palmar cutaneous branch: a case study with clinical implications.

IF 1.2 4区 医学 Q3 ANATOMY & MORPHOLOGY Anatomical Science International Pub Date : 2024-12-09 DOI:10.1007/s12565-024-00817-y
Sajad Seyyedin, Seyed Noureddin Nematollahi-Mahani
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Abstract

The median artery typically regresses after two months of intrauterine life, although it may persist into adulthood in some individuals. The presence of a persistent median artery (PMA) may be associated with other anatomical variations including a bifid median nerve. In the present cadaveric study, we report a rare variation of bilateral asymmetry of PMA associated with the bifid median nerve, and unilateral variation of the origin and course of the palmar cutaneous branch of the median nerve (PCBMN) which to our knowledge, is the first study to report all these variations in an individual. Classical dissection of the upper limb was performed on a 45-year-old male cadaver. The cadaver was donated to the Department of Anatomy at Kerman University of Medical Sciences. Bilateral PMA was observed in both upper limbs. The PMA originated from the ulnar artery and contributed to the formation of an incomplete superficial palmar arch (SPA) on both sides; however, the branching pattern of these arteries was different between the right and left hands. Also, a bilateral high division of the median nerve was observed proximal to the carpal tunnel. We also encountered a very rare variation of PCBMN, in which it originated from the ulnar side of the median nerve, and passed beneath the flexor retinaculum of the left hand. Awareness of anatomical variations of the median nerve and also the presence of PMA is of utmost importance due to their implication in carpal tunnel syndrome and surgical complications.

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双侧正中动脉与双裂正中神经共存时的不对称变异及其掌皮支起源和走向的变异:一个具有临床意义的病例研究。
正中动脉通常会在宫内生活两个月后消退,但有些人可能会持续到成年。正中动脉持续存在(PMA)可能与其他解剖变异有关,包括正中神经分叉。在本尸体研究中,我们报告了一种罕见的变异,即正中神经双侧不对称,正中神经掌皮支(PCBMN)的起源和走向单侧变异。我们对一具 45 岁的男性尸体进行了上肢经典解剖。这具尸体捐赠给了克尔曼医科大学解剖学系。在双上肢均观察到双侧 PMA。PMA 起源于尺动脉,并在两侧形成了不完整的掌浅弓(SPA);然而,这些动脉的分支模式在左右手中有所不同。此外,在腕管近端还观察到双侧正中神经高位分叉。我们还发现了一种非常罕见的 PCBMN 变异,即它起源于正中神经的尺侧,并从左手屈肌腱膜下方穿过。认识正中神经的解剖变异以及 PMA 的存在至关重要,因为它们会导致腕管综合征和手术并发症。
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来源期刊
Anatomical Science International
Anatomical Science International 医学-解剖学与形态学
CiteScore
2.80
自引率
8.30%
发文量
50
审稿时长
>12 weeks
期刊介绍: The official English journal of the Japanese Association of Anatomists, Anatomical Science International (formerly titled Kaibogaku Zasshi) publishes original research articles dealing with morphological sciences. Coverage in the journal includes molecular, cellular, histological and gross anatomical studies on humans and on normal and experimental animals, as well as functional morphological, biochemical, physiological and behavioral studies if they include morphological analysis.
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