Piazza C, Casirati C, Peretti G, Battaglia G, Manfredini C, Nicolai P
Department of Otolaryngology, University of Brescia, Italy.
Head Neck. 2000 Aug;22(5):524-9. doi: 10.1002/1097-0347(200008)22:5<524::aid-hed14>3.0.co;2-d.
Granular cell tumor (GCT), or Abrikossoff's tumor, is an unusual lesion probably arising from Schwann cells. It is frequently found in the head and neck region, where the tongue is the most commonly affected site. Involvement of the hypopharynx is exceedingly rare because, to the best of our knowledge, only four cases have been reported in the literature.
We describe hypopharyngeal GCT in two women aged 29 and 52 years, respectively.
In the first patient, preoperative diagnostic examination, including endoscopy, CT, and MRI scan, was suggestive of a benign lesion arising from the posterior wall of the hypopharynx. In the second patient, a previous biopsy of the postcricoid area performed elsewhere suggested a diagnosis of well-differentiated squamous cell carcinoma, and CT scan staged the lesion as T1 N0. In both cases, treatment included surgical excision under microlaryngoscopy with CO(2) laser. The histopathologic study of the specimens, supported by immunohistochemical techniques, determined the lesions to be a GCT. The postoperative course was uneventful, and the patients were discharged 12 and 2 days after surgery, respectively. Both patients were asymptomatic without evidence of recurrence when last seen 2 years and 4 months after surgery, respectively.
GCT should be included in the differential diagnosis of submucosal hypopharyngeal lesions. Endoscopy and radiologic imaging do not display any typical finding suggestive of the diagnosis, which can be based only on histologic findings. Resection of the tumor, when technically feasible, should be performed under microlaryngoscopy with the CO(2) laser, which makes it possible to work in a bloodless field with minimal thermal damage and reduction of scarring and postoperative edema.
颗粒细胞瘤(GCT),即阿布里科索夫瘤,是一种可能起源于施万细胞的罕见病变。它常见于头颈部区域,其中舌是最常受累的部位。下咽受累极为罕见,据我们所知,文献中仅报道过4例。
我们分别描述了两名年龄为29岁和52岁女性的下咽颗粒细胞瘤。
首例患者的术前诊断检查,包括内镜检查、CT和MRI扫描,提示病变起源于下咽后壁,为良性病变。第二例患者,此前在其他地方对环状软骨后区域进行的活检提示诊断为高分化鳞状细胞癌,CT扫描将病变分期为T1 N0。两例患者均接受了在显微喉镜下用二氧化碳激光进行的手术切除。标本的组织病理学研究在免疫组化技术的支持下确定病变为颗粒细胞瘤。术后过程顺利,患者分别在术后12天和2天出院。分别在术后2年和4个月最后一次就诊时,两名患者均无症状,无复发迹象。
颗粒细胞瘤应列入下咽黏膜下病变的鉴别诊断中。内镜检查和影像学检查未显示任何提示诊断的典型表现,诊断只能基于组织学检查结果。在技术可行的情况下,应在显微喉镜下用二氧化碳激光切除肿瘤,这使得手术能够在无血的视野中进行,热损伤最小,减少瘢痕形成和术后水肿。