表现为先天性巨指症的帕西尼神经瘤：一例罕见病例报告
Pacinian Neuroma Presenting as Congenital Macrodactyly: A Rare Case Report.
作者信息
Mahipathy Surya Rao Rao Venkata, Durairaj Alagar Raja, Parthasarathy Jayaganesh
机构信息
Associate Professor, Department of Plastic Surgery, Saveetha Medical College Hospital , Thandalam, Kanchipuram, India .
Associate Professor, Department of Pathology, Saveetha Medical College Hospital , Thandalam, Kanchipuram, India .
出版信息
J Clin Diagn Res. 2015 Sep;9(9):PD22-3. doi: 10.7860/JCDR/2015/14525.6528. Epub 2015 Sep 1.
Pacinian neuromas are rare benign tumours of pacinian corpuscles of the digits. They generally occur on the volar aspect of the fingertips. Pacinian corpuscles are specialised nerve endings with a lamellated structure and are regarded as pressure and vibration receptors. Here, we report a case of pacinian neuroma presenting as congenital macrodactyly of the right little finger with pain for which the lesion was surgically excised.
帕西尼神经瘤是一种罕见的手指帕西尼小体良性肿瘤。它们通常发生在指尖掌侧。帕西尼小体是具有层状结构的特殊神经末梢，被视为压力和振动感受器。在此，我们报告一例表现为右小指先天性巨指症并伴有疼痛的帕西尼神经瘤病例，该病变已通过手术切除。
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