Javaroni Julia Biliato, Silveira Heitor Albergoni, Reyes Magdalena Raquel Torres, Mesquita Ana Terezinha Marques, Rocha Gabriela Fonseca, León Jorge Esquiche
Department of Pediatric Dentistry - Riberão Preto Dental School (FORP/USP), University of São Paulo, Ribeirão Preto, SP Brazil.
Oral Pathology, Department of Stomatology, Public Oral Health, and Forensic Dentistry, Ribeirão Preto Dental School (FORP/USP), University of São Paulo, Avenida do Café, S/N, Ribeirão Preto, SP 14040-904 Brazil.
Indian J Otolaryngol Head Neck Surg. 2023 Dec;75(4):3920-3924. doi: 10.1007/s12070-023-03957-1. Epub 2023 Jun 17.
Granular cell tumor (GCT) is an uncommon benign neoplasm derived from Schwann cells, frequently affecting the oral cavity, skin, and gastrointestinal tract. On microscopy, pseudocarcinomatous squamous hyperplasia (PSH) and perineural involvement are potential diagnostic pitfalls. GCT should be differentiated from non-neural GCT (NN-GCT). A 13-year-old male patient was referred presenting a nodular lesion on the upper lip several months ago. After excisional biopsy, microscopy revealed GCT without PSH but presenting multifocal perineural involvement. By immunohistochemistry, ALK was negative, whereas Rb and INI1 expression was intact. Moreover, with few intraoral NN-GCTs being assessed, recent studies suggest that acquired dermal NN-GCT subgroup seems to correspond to ALK-rearranged variants of epithelioid fibrous histiocytoma. Accordingly, further research on this topic is strongly encouraged.
颗粒细胞瘤(GCT)是一种罕见的源自施万细胞的良性肿瘤,常累及口腔、皮肤和胃肠道。在显微镜下,假癌性鳞状上皮增生(PSH)和神经周围侵犯是潜在的诊断陷阱。GCT应与非神经颗粒细胞瘤(NN-GCT)相鉴别。一名13岁男性患者数月前因上唇出现结节性病变前来就诊。切除活检后,显微镜检查显示为无PSH但有多灶性神经周围侵犯的GCT。免疫组化显示,间变性淋巴瘤激酶(ALK)为阴性,而视网膜母细胞瘤(Rb)和整合素结合蛋白1(INI1)表达完整。此外,由于评估的口腔内NN-GCT较少,近期研究表明,获得性皮肤NN-GCT亚组似乎对应于上皮样纤维组织细胞瘤的ALK重排变体。因此,强烈鼓励对此主题进行进一步研究。