Leach Brian C, Kulbersh Jonathan S, Day Terry A, Cook Joel
Department of Dermatology, Medical University of South Carolina, Charleston, South Carolina 29425, USA.
Dermatol Surg. 2008 Apr;34(4):483-97. doi: 10.1111/j.1524-4725.2007.34094.x. Epub 2008 Jan 31.
The purpose of this study was to identify and characterize recurrent skin cancers of the head and neck presenting with cranial neuropathies and to review the presentation and the management for this rare subset of cutaneous neoplasms.
A retrospective review was performed for all patients with previous related cutaneous neoplasms presenting with cranial neuropathies referred to a single academic tertiary-care head and neck tumor program from 1999 to 2007. Six cases of head and neck carcinoma with demonstrable cranial neuropathy were identified and analyzed by clinical history, radiographic and surgical findings, and treatment and survival data. A review of the literature, pertinent anatomy, imaging studies, and surgical/nonsurgical management are summarized for these aggressive neurotropic malignancies.
Cranial neuropathy was the presenting symptom of recurrent disease in all six patients. Four presented with multiple cranial neuropathies. All exhibited neuropathy of the trigeminal nerve (cranial nerve V). The tumors involved were squamous cell carcinoma (4) and melanoma (2). All patients were multiply symptomatic, presenting with a mean of three neurologic symptoms, including facial numbness (5), facial paralysis or weakness (3), facial pain (3), diplopia (3), paresthesia (3), hearing loss (1), or formication (2). Symptoms were present for an average of 7 months prior to diagnosis of perineural recurrence. Cranial nerve involvement was confirmed in all patients by magnetic resonance imaging, and five patients manifested histologic evidence of perineural tumor infiltration. Treatment consisted of various combinations of surgery, radiation, and chemotherapy for five patients, and one patient declined any intervention. Death rate subsequent to disease was 50%, and follow-up has continued within our institution on all patients for an average of 25.5 months (range, 3-72 months).
Cranial neuropathy is a rare presentation of recurrent cutaneous neoplasms of the head and neck. Given this infrequent occurrence and shared features of presentation, these highly morbid tumors are often mistakenly diagnosed as Bell's palsy or trigeminal neuralgia. Our findings corroborate previous reports of diagnostic delay, increased tumor burden, and worsened morbidity and mortality associated with such cutaneous malignancies. The critical utility of radiologic imaging for staging and tumor delineation are also supported by our institutional data.
本研究旨在识别和描述伴有颅神经病变的头颈部复发性皮肤癌,并回顾这一罕见皮肤肿瘤亚组的临床表现及治疗方法。
对1999年至2007年转诊至单一学术性三级医疗头颈肿瘤项目、既往有相关皮肤肿瘤且伴有颅神经病变的所有患者进行回顾性研究。通过临床病史、影像学和手术结果以及治疗和生存数据,对6例伴有可证实颅神经病变的头颈癌患者进行了识别和分析。对这些侵袭性嗜神经性恶性肿瘤的文献、相关解剖学、影像学研究以及手术/非手术治疗进行了总结。
颅神经病变是所有6例患者复发性疾病的首发症状。4例患者表现为多发性颅神经病变。所有患者均表现出三叉神经(颅神经V)神经病变。所涉及的肿瘤为鳞状细胞癌(4例)和黑色素瘤(2例)。所有患者均有多种症状,平均出现3种神经症状,包括面部麻木(5例)、面瘫或肌无力(3例)、面部疼痛(3例)、复视(3例)、感觉异常(3例)、听力丧失(1例)或蚁走感(2例)。症状在诊断神经周围复发前平均出现7个月。所有患者均通过磁共振成像证实有颅神经受累,5例患者有神经周围肿瘤浸润的组织学证据。5例患者接受了手术、放疗和化疗的各种联合治疗,1例患者拒绝任何干预。疾病发生后的死亡率为50%,本机构对所有患者继续进行了平均25.5个月(范围3 - 72个月)的随访。
颅神经病变是头颈部复发性皮肤肿瘤的罕见表现。鉴于这种情况罕见且临床表现有共同特征,这些高发病率肿瘤常被误诊为贝尔麻痹或三叉神经痛。我们的研究结果证实了先前关于诊断延迟、肿瘤负荷增加以及与此类皮肤恶性肿瘤相关的发病率和死亡率恶化的报道。我们机构的数据也支持了放射影像学在分期和肿瘤勾画方面的关键作用。