PDF(Pubmed)
Abstract：
Granular cell tumours (GCTs) are rare soft tissue tumours of neural origin. They have been reported in multiple anatomical sites. However, only 14 cases worldwide have been reported arising from the abdominal wall. While they can clinically manifest in a variety of ways, often they present as a small, slow-growing nodule with benign features. They can, however, be malignant, and in rare cases, they have been reported to metastasise. Here, we present a case of a rare abdominal wall GCT, which was managed with local excision. The purpose of this paper is to report the patient\'s clinical history, presentation, and surgical management, as well as to review the current literature to highlight the existence of this rare entity and the possibility that this may occur and should be considered a differential diagnosis in clinical practice.
摘要：
颗粒细胞肿瘤（GCT）是罕见的神经起源的软组织肿瘤。它们已经在多个解剖部位被报道。然而,全世界仅报告了14例由腹壁引起的病例.虽然它们可以通过多种方式在临床上表现出来，他们经常作为一个小的，具有良性特征的缓慢生长结节。他们可以,然而,是恶性的，在极少数情况下，据报道它们会转移。这里,我们介绍了一例罕见的腹壁GCT,这是通过局部切除来管理的。本文的目的是报告患者的临床病史，介绍,和手术管理，以及回顾当前的文献，以强调这种罕见实体的存在以及可能发生这种情况的可能性，并应将其视为临床实践中的鉴别诊断。
