Batten Rebecca L, Ng Wan-Fai
Clinical Research Facility, Level 6, Leazes Wing, Royal Victoria Infirmary, Newcastle upon Tyne NE1 4PE, UK.
J Med Case Rep. 2014 Mar 25;8:105. doi: 10.1186/1752-1947-8-105.
We report an unusual case of facial pain and swelling caused by compression of the facial and vestibulocochlear cranial nerves due to the tortuous course of a branch of the posterior inferior cerebellar artery. Although anterior inferior cerebellar artery compression has been well documented in the literature, compression caused by the posterior inferior cerebellar artery is rare. This case provided a diagnostic dilemma, requiring expertise from a number of specialties, and proved to be a learning point to clinicians from a variety of backgrounds. We describe the case in detail and discuss the differential diagnoses.
A 57-year-old Caucasian woman with a background of mild connective tissue disease presented to our rheumatologist with intermittent left-sided facial pain and swelling, accompanied by hearing loss in her left ear. An autoimmune screen was negative and a Schirmer's test was normal. Her erythrocyte sedimentation rate was 6mm/h (normal range: 1 to 20mm/h) and her immunoglobulin G and A levels were mildly elevated. A vascular loop protocol magnetic resonance imaging scan showed a loop of her posterior inferior cerebellar artery taking a long course around the seventh and eighth cranial nerves into the meatus and back, resulting in compression of her seventh and eighth cranial nerves. Our patient underwent microvascular decompression, after which her symptoms completely resolved.
Hemifacial spasm is characterized by unilateral clonic twitching, although our patient presented with more unusual symptoms of pain and swelling. Onset of symptoms is mostly in middle age and women are more commonly affected. Differential diagnoses include trigeminal neuralgia, temporomandibular joint dysfunction, salivary gland pathology and migrainous headache. Botulinum toxin injection is recognized as an effective treatment option for primary hemifacial spasm. Microvascular decompression is a relatively safe procedure with a high success rate. Although a rare pathology, posterior inferior cerebellar artery compression causing facial pain, swelling and hearing loss should be considered as a differential diagnosis in similar cases.
我们报告一例不寻常的病例,因小脑后下动脉分支走行迂曲,压迫面神经和前庭蜗神经,导致面部疼痛和肿胀。尽管文献中已充分记载了小脑前下动脉压迫的情况,但小脑后下动脉引起的压迫却很罕见。该病例带来了诊断难题,需要多个专科的专业知识,并且对来自各种背景的临床医生来说都是一个学习点。我们详细描述该病例并讨论鉴别诊断。
一名57岁有轻度结缔组织病病史的白种女性,因间歇性左侧面部疼痛和肿胀,伴有左耳听力丧失,前来我们的风湿病科就诊。自身免疫筛查为阴性,泪液分泌试验正常。她的红细胞沉降率为6mm/h(正常范围:1至20mm/h),免疫球蛋白G和A水平轻度升高。血管袢协议磁共振成像扫描显示,她的小脑后下动脉袢沿着第七和第八颅神经走行很长一段距离进入耳道并折返,导致第七和第八颅神经受压。我们的患者接受了微血管减压术,术后症状完全缓解。
面肌痉挛的特征是单侧阵挛性抽搐,尽管我们的患者表现出更不寻常的疼痛和肿胀症状。症状多在中年起病,女性更易受累。鉴别诊断包括三叉神经痛、颞下颌关节功能障碍、唾液腺病变和偏头痛性头痛。肉毒杆菌毒素注射被认为是原发性面肌痉挛的有效治疗选择。微血管减压术是一种相对安全且成功率高的手术。尽管是一种罕见的病理情况,但小脑后下动脉压迫导致面部疼痛、肿胀和听力丧失,在类似病例中应作为鉴别诊断考虑。