Ugur Kesici, Emine Mataraci, Sevgi Kesici, Sezgin Zeren
Department of General Surgery, Ministry of Health, Akcaabat Hackali Baba State Hospital, Trabzon, Turkey.
Acta Med Iran. 2013 Aug 7;51(7):509-11.
Granular cell tumor (GCT) was first described by Abrikossoff in 1926. GCT is a rarely seen soft tissue tumor and is generally benign. While the tumor can be seen in all parts of the body it is generally located on the head and neck region, and especially on the tongue. GCT is rarely seen in the anal-perianal region. In accordance with literature this case was reported because it was thought to be the 27th anal-perianal located GCT case. In this case report, approximately 0,5-1 cm pedunculated polypoid lesion was determined in the perianal region during the physical examination of a 23 year old female patient who applied with palpable mass complaint in the perianal region. Lesion in the patient was totally excited with healthy skin-subcutaneous tissue under local anesthesia. A benign granular cell tumor was detected in the histopathological examination. Positive staining was monitored immunohistochemically with S-100 and neuron specific enolase (NSE). GCT is a rarely seen tumor in the anal-perianal region and its malign transformation rate is very low. Even lesions seen in the perianal region have clinically a benign appearance, a histopathological examination should be conducted and also GCT should be kept in mind during diagnosis. Malign-benign separation of these lesions is difficult so histopathological examination should be conducted with great care. Large local excision in the treatment provides curative treatment. But for those presenting malign transformation further examination must be performed for metastasis. After the treatment local recurrence and metastasis should be considered carefully. Prognosis of metastatic disease is very bad.
颗粒细胞瘤(GCT)于1926年由阿布里科索夫首次描述。GCT是一种罕见的软组织肿瘤,通常为良性。虽然该肿瘤可见于身体的各个部位,但一般位于头颈部区域,尤其是舌头。GCT在肛门-肛周区域很少见。根据文献报道,该病例被认为是第27例位于肛门-肛周的GCT病例。在本病例报告中,一名23岁女性患者因肛周可触及肿块前来就诊,体格检查时在肛周区域发现一个约0.5 - 1厘米的带蒂息肉样病变。在局部麻醉下,将患者病变连同健康的皮肤-皮下组织完整切除。组织病理学检查发现为良性颗粒细胞瘤。免疫组织化学检测S - 100和神经元特异性烯醇化酶(NSE)呈阳性染色。GCT在肛门-肛周区域是一种罕见的肿瘤,其恶变率非常低。即使在肛周区域见到的病变临床外观为良性,也应进行组织病理学检查,并且在诊断时应考虑到GCT。这些病变的良恶性鉴别困难,因此组织病理学检查应格外谨慎。治疗采用局部广泛切除可治愈。但对于出现恶变的患者,必须进一步检查是否有转移。治疗后应仔细考虑局部复发和转移情况。转移性疾病的预后非常差。