Georgiev G P, Jelev L
Department of Anatomy, Histology and Embryology, Medical University, Sofia, Bulgaria.
Rom J Morphol Embryol. 2009;50(4):725-7.
During routine anatomical dissection of the left upper limb of a 73-year-old female cadaver, a unique coexistence of variant muscles was found. In the forearm region, a largely developed reversed palmaris longus was discovered. Its short distal tendon was in close relation to the median nerve. In the neighboring hypothenar region, an unusual abductor digiti minimi was also observed. Its muscular body was composed of two portions - medial and lateral one, arising from the reversed palmaris longus tendon. The lateral portion passed over the ulnar nerve and artery in the canal of Guyon. In the literature, there are descriptions of entrapment neuropathies caused by either reversed palmaris longus or variant abductor digiti minimi. Here, for the first time we describe a coexistence of these variant muscles and suggest it as a possible, even rare, cause of both the median and ulnar nerves entrapment and ulnar artery thrombosis.
在对一名73岁女性尸体的左上肢进行常规解剖时,发现了一种独特的变异肌肉共存情况。在前臂区域,发现了一块发育较大的反掌长肌。其短的远端肌腱与正中神经关系密切。在相邻的小鱼际区域,还观察到一块异常的小指展肌。其肌腹由两部分组成——内侧部分和外侧部分,起自反掌长肌腱。外侧部分在Guyon管内越过尺神经和尺动脉。文献中有关于反掌长肌或变异小指展肌导致卡压性神经病的描述。在此,我们首次描述了这些变异肌肉的共存情况,并认为这可能是导致正中神经和尺神经卡压以及尺动脉血栓形成的一个原因,尽管这种情况可能很罕见。