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[病例报告:鼻侧壁多形性腺瘤]

[Case report: pleomorphic adenoma of the lateral nasal wall].

作者信息

Castello E, Caligo G, Pallestrini E A

机构信息

Dipartimento Regionale Testa Collo, Ospedale San Martino, Genova.

出版信息

Acta Otorhinolaryngol Ital. 1996 Oct;16(5):433-7.

PMID:9199088
Abstract

Pleomorphic adenoma is a tumor which most often originates from one of the major salivary glands; it is rarely located in the lacrymal glands and it is highly exceptional in the nasal cavity. Cases of pleomorphic adenoma in the nasal cavity have been described by Spiro (40 cases), Compagno and Wong (40 cases) and Suzuki et al. (41 cases). This type of tumor generally originates from the septal mucosa even though the seromucosal glands are mostly located in the lateral nasal wall. This pathology is more frequently found in females. The clinical signs of this tumor are non specific, slow unilateral nasal occlusion, rhinorrhea and, at times, epistaxis. Evolution is generally local although locoregional and distant metastases have been described in the literature. This sort of tumor has no specific appearance and thus diagnosis is based on histology. Indeed, microscopically nasal pleomorphic adenoma differs from salivary gland adenoma for the predominance of the cellular component over the connective component. The epithelial cells are small, oval-shaped and often arranged in cordons; they are sometimes organized in small acinous structures. The connective component can be mixoid, condroid or collagenous; follicles with squamous metaplasia and mitosis are rare. Histologically differentiating this disorder from olfactory esthesione-uroblastoma can prove difficult; the lack of extra cellular neurifibrillar structures, neurotubules and neurosecretory granules in nasal pleomorphic adenoma are the main distinguishing criteria. The present work reports a case of a 45-year-old man who had suffered of an increasing unilateral nasal obstruction from 1 year. Endoscopic examination showed a smooth surface neoplasm involving the entire nasal cavity. CT scan showed the deformation of the medial bone wall of the maxillary sinus and of the ethmoid although without any osteolysis. Median maxillectomy surgical exeresis of the neoplasm was performed with the facial degloving technique. Histology revealed a 5 cm pleomorphic adenoma originating from the lateral nasal wall. This origin is extremely rare because this tumor generally originates in the nasal septum. Immunohistochemical stains proved positive for epithelial membrane antigen (MNF 116), for myoepithelial cells (PS100) and for stromal cells (Vimentine) with the epithelial elements predominating. After 9 months of follow-up the patient is still disease free.

摘要

多形性腺瘤是一种最常起源于大唾液腺之一的肿瘤;它很少位于泪腺,在鼻腔中极为罕见。鼻腔多形性腺瘤的病例已由斯皮罗(40例)、孔帕尼奥和王(40例)以及铃木等人(41例)进行过描述。这种类型的肿瘤通常起源于鼻中隔黏膜,尽管浆液黏液腺大多位于鼻侧壁。这种病理情况在女性中更常见。该肿瘤的临床症状不具有特异性,表现为缓慢的单侧鼻塞、流涕,有时还有鼻出血。虽然文献中描述过局部区域和远处转移,但肿瘤通常呈局部进展。这种肿瘤没有特异性外观,因此诊断基于组织学。实际上,显微镜下鼻腔多形性腺瘤与唾液腺腺瘤的不同之处在于细胞成分比结缔组织成分占优势。上皮细胞小,呈椭圆形,常排列成索状;有时会组织成小的腺泡结构。结缔组织成分可以是黏液样、软骨样或胶原样;有鳞状化生和有丝分裂的滤泡很少见。从组织学上区分这种疾病与嗅神经母细胞瘤可能很困难;鼻腔多形性腺瘤中缺乏细胞外神经纤维结构、神经微管和神经分泌颗粒是主要的鉴别标准。本研究报告了一例45岁男性患者,他单侧鼻塞加重已有1年。内镜检查显示鼻腔内有一个表面光滑的肿物。CT扫描显示上颌窦内侧骨壁和筛骨变形,尽管没有任何骨质溶解。采用面部掀翻技术进行了肿瘤的上颌骨中位切除术。组织学检查显示为一个起源于鼻侧壁的5厘米多形性腺瘤。这种起源极为罕见,因为这种肿瘤通常起源于鼻中隔。免疫组化染色显示上皮膜抗原(MNF 116)、肌上皮细胞(PS100)和基质细胞(波形蛋白)呈阳性,上皮成分占主导。随访9个月后,患者仍无疾病复发。

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