Nasit Jitendra G, Chauhan Sanjaykumar, Dhruva Gauravi
Department of Pathology, P. D. U. Government Medical College and Hospital, Rajkot, Gujarat, India.
Indian Dermatol Online J. 2013 Jan;4(1):33-6. doi: 10.4103/2229-5178.105467.
Granular cell tumor (GCT) is an uncommon tumor and is believed to be of schwannian origin. GCT is benign but rare malignant cases are recorded. GCT occurs in almost any part of the body. The common sites are the tongue, skin, and subcutaneous tissue. GCT of hand is an extremely rare. Till date only 17 cases are reported in the literature. Preoperative diagnosis of GCT is important, because GCT mimics dermal adnexal tumor in subcutaneous tissue, other soft tissue tumor or inflammatory lesions. GCT is composed of large polygonal cells with eosinophilic granular cytoplasm and these cells are often immunoreactive for the S-100 protein. Fine-needle aspiration cytology has been suggested to be diagnostic modality of choice and this would undoubtedly aid the correct diagnosis. Excision with wide surgical margins is curative for benign GCT. Recurrence and malignant transformation requires regular follow-up. Here, this communication documents a case of cytological diagnosis of the granular cell tumor of hand in a 21-year-old female, clinically suspected to be a dermal adnexal tumor.
颗粒细胞瘤(GCT)是一种罕见肿瘤,被认为起源于施万细胞。GCT通常为良性,但也有罕见的恶性病例报道。GCT可发生于身体几乎任何部位,常见部位为舌、皮肤和皮下组织。手部GCT极为罕见,迄今为止,文献中仅报道了17例。GCT的术前诊断很重要,因为GCT在皮下组织中可类似皮肤附属器肿瘤、其他软组织肿瘤或炎性病变。GCT由具有嗜酸性颗粒状细胞质的大的多边形细胞组成,这些细胞通常对S-100蛋白呈免疫反应性。细针穿刺细胞学检查被认为是首选的诊断方法,这无疑有助于正确诊断。良性GCT通过广泛手术切缘切除可治愈。复发和恶性转化需要定期随访。在此,本文报道了一例21岁女性手部颗粒细胞瘤的细胞学诊断病例,该病例临床怀疑为皮肤附属器肿瘤。