Department of Pathology & Laboratory Medicine, All India Institute of Medical Sciences (AIIMS), Rishikesh, India.
Department of Pathology, Atal Bihari Vajpayee Institute of Medical Sciences (Formerly PGIMER), Dr Ram Manohar Lohia Hospital, New Delhi, India.
Head Neck Pathol. 2022 Sep;16(3):707-715. doi: 10.1007/s12105-022-01415-y. Epub 2022 Feb 14.
Schwannoma is a benign, slow growing, usually solitary and encapsulated tumor derived from Schwann cells of the nerve sheath. Schwannomas can be divided into central, or intraosseous, and peripheral lesions. The etiology is unknown, but it is postulated that lesions arise by the proliferation of Schwann cells at one point inside the perineurium. Schwannomas may mimic other diseases of the head and neck, such as infection, tumor or metastasis. Extracranial schwannomas are rare; in this study we review a series of 22 cases of schwannomas originating in the head and neck region over a period of eight years. All tumors were benign and well-encapsulated. Tumor size ranged from 0.5 to 9 cm. The age range of patients studied was 15-74 years with a mean age of 35 years and a male predilection (M:F, 2.6:1)was noted. Four cases of schwannomas occurred in the tongue (18.18%) and lower lip (18.18%), three in the nasal cavity (13.64%), two each (9.09%) in the buccal mucosa, parapharyngeal space (9.09%), and eyebrow (9.09%), and one each in the upper lip (4.55%), lateral canthus of the eye (4.55%), intraorbital region (4.55%), submandibular gland (4.55%), and ear (4.55%). Schwannomas can present in a wide variety of sites within the head and neck. The tumor is benign and tend to be asymptomatic for long periods of time. Histopathology is the gold standard for diagnosis. Our study describes the clinicopathologic features of extracranial head and neck schwannomas, highlights the histopathologic features, and discusses pertinent findings with correlation to the present literature. It is important that both clinicians and pathologists be familiar with the uncommon sites of occurrence and the potential pitfalls associated with the diagnosis and management of these tumors.
神经鞘瘤是一种良性、生长缓慢的肿瘤,通常为单发、包膜完整,来源于神经鞘细胞。神经鞘瘤可分为中枢性(或骨内)和周围性病变。其病因不明,但推测病变是由神经外膜内一点的雪旺氏细胞增殖引起的。神经鞘瘤可能模仿头颈部的其他疾病,如感染、肿瘤或转移。颅外神经鞘瘤很少见;在这项研究中,我们回顾了八年来起源于头颈部的 22 例神经鞘瘤病例。所有肿瘤均为良性且包膜完整。肿瘤大小从 0.5 厘米至 9 厘米不等。研究对象的年龄范围为 15-74 岁,平均年龄为 35 岁,且存在男性偏好(男:女,2.6:1)。4 例神经鞘瘤发生于舌(18.18%)和下唇(18.18%),3 例发生于鼻腔(13.64%),2 例分别发生于颊黏膜、咽旁间隙(9.09%)和眉弓(9.09%),1 例分别发生于上唇(4.55%)、外眦(4.55%)、眼眶内(4.55%)、下颌下腺(4.55%)和耳部(4.55%)。神经鞘瘤可发生于头颈部的广泛部位。肿瘤为良性,往往长时间无症状。组织病理学是诊断的金标准。我们的研究描述了颅外头颈部神经鞘瘤的临床病理特征,强调了组织病理学特征,并结合现有文献讨论了相关发现。临床医生和病理学家都熟悉这些肿瘤的罕见发生部位和诊断及治疗相关的潜在陷阱非常重要。