Khader Abul Hasan Shadali Abdul, Sivasubramanian Barath Prashanth, Ravikumar Diviya Bharathi, Rajkumar Nithyalakshmi, Rajakannu Gokul, Tirupathi Raghavendra
Department of Internal Medicine, Government Kilpauk Medical College, Chennai, India.
Department of Infectious Diseases, University of Texas Health Science Centre, San Antonio, TX, United States.
J Community Hosp Intern Med Perspect. 2023 Nov 4;13(6):71-75. doi: 10.55729/2000-9666.1267. eCollection 2023.
Multiple cranial nerve palsies frequently accompany hypoglossal nerve palsy, potentially indicating malignancy, such as lymphoma, nasopharyngeal carcinoma, or metastases. However, when solely the hypoglossal nerve is affected, the causes may involve Chiari malformation, arachnoid cyst, or infectious mononucleosis, suggesting a positive prognosis. Craniocervical junction tuberculosis (TB), is an uncommon cause of isolated hypoglossal nerve palsy and has been reported infrequently in the literature. Craniocervical junction tuberculosis accounts for only 0.5% of TB cases overall and 6% of extra-pulmonary TB cases. We present here one such case of a 17-year-old male of Indian origin with a subacute history of tongue deviation and neck pain. Additionally, the patient reported loss of weight and appetite. The patient had significant posterior cervical lymphadenopathy. Neurological examination revealed findings suggestive of right peripheral hypoglossal nerve involvement. Blood investigations showed lymphocytosis along with an elevated erythrocyte sedimentation rate of 45 mm/h and elevated lactate dehydrogenase levels of 325 U/L. Tuberculin skin testing was positive and sputum acid-fast staining confirmed acid-fast bacilli. Magnetic Resonance Imaging of the cervical spine revealed a soft tissue component in the prevertebral space measuring 3.5×4.8 cm with a right paraspinal component adjoining the hypoglossal canal with peripheral contrast enhancement. Histological findings on the lymph node showed granulomatous lymphadenitis, suggestive of tuberculosis. The patient was started on 4-drug anti-tubercular therapy consisting of Isoniazid, Rifampicin, Pyrazinamide, and Ethambutol for a period of 18 months. He was subsequently followed up for 6 months till the resolution of palsy. This case emphasizes the importance of thorough evaluation and a meticulous workup to identify the underlying cause of hypoglossal nerve palsy and the importance of considering tuberculosis as a potential cause of isolated hypoglossal nerve palsy in everyday practice.
多组颅神经麻痹常伴有舌下神经麻痹,这可能提示恶性肿瘤,如淋巴瘤、鼻咽癌或转移瘤。然而,当仅舌下神经受累时,病因可能包括Chiari畸形、蛛网膜囊肿或传染性单核细胞增多症,提示预后良好。颅颈交界区结核是孤立性舌下神经麻痹的罕见病因,文献报道较少。颅颈交界区结核仅占所有结核病例的0.5%,占肺外结核病例的6%。我们在此报告一例17岁印度裔男性病例,该患者有舌偏斜和颈部疼痛的亚急性病史。此外,患者自述体重减轻和食欲减退。患者有明显的颈后淋巴结肿大。神经系统检查发现提示右侧周围性舌下神经受累。血液检查显示淋巴细胞增多,红细胞沉降率升高至45mm/h,乳酸脱氢酶水平升高至325U/L。结核菌素皮肤试验呈阳性,痰涂片抗酸染色发现抗酸杆菌。颈椎磁共振成像显示椎前间隙有一软组织成分,大小为3.5×4.8cm,右侧椎旁成分毗邻舌下神经管,周边有对比增强。淋巴结组织学检查显示肉芽肿性淋巴结炎,提示为结核。该患者开始接受为期18个月的由异烟肼、利福平、吡嗪酰胺和乙胺丁醇组成的四联抗结核治疗。随后对其进行了6个月的随访,直至麻痹症状消失。该病例强调了全面评估和细致检查以确定舌下神经麻痹潜在病因的重要性,以及在日常实践中考虑结核作为孤立性舌下神经麻痹潜在病因的重要性。