Ghannane Houssine, Laghmari Mehdi, Aniba Khalid, Lmejjati Mohammed, Benali Saïd Ait
Department of Neurosurgery, UHC Mohammed VI, Faculty of Medicine, Cadi Ayyad University, Marrakesh, Morocco.
Childs Nerv Syst. 2011 Jul;27(7):1053-62. doi: 10.1007/s00381-011-1441-x. Epub 2011 Apr 6.
Authors report their experience of a pediatric brain stem abscess with a literature review.
A 2.5-year-old girl first displayed bacterial otitis 3 months before admission. Diagnosis of brain stem abscess was delayed, despite plethoric neurological signs. She complained of right hemiparesis, headache, squint, dysphagia, and false way inhalation pneumopathy. Brain magnetic resonance imaging revealed presence of an abscess in the pons, prompting for a microsurgical pus aspiration. Postoperative course was regular with a total neurological recovery. Clinical and radiological screening showed progressive regression of the pontine lesion after 4 months, despite persistence of a mild contrast enhancement. Present case is the 18th pediatric brain stem abscess reported in literature.
Mean age of occurrence is 8.1 ± 4 years (range 0.75-16) without gender predominance. High morbidity is typical and essentially involves motor functions. The most common clinical signs are raised intracranial pressure, motor limbs deficit, and cranial nerve palsies. Fever was found in 10 out of 18 cases (56%). Three patients received conservative medical treatment. Three patients underwent stereotactic aspiration and 12 others underwent microsurgical aspiration or excision. No mortality was reported since the eighties. However, morbidity is still high.
High clinical index of suspicion is necessary to improve functional outcome. Stereotactic-guided or microsurgical aspiration are still good therapeutic options. The rarity of pediatric brain stem abscesses and the need of optimal management make this case-based update very peculiar.
作者报告了一例小儿脑干脓肿的诊治经验并进行文献复习。
一名2.5岁女童在入院前3个月首次出现细菌性中耳炎。尽管存在明显的神经系统体征,但脑干脓肿的诊断仍被延误。她主诉右侧偏瘫、头痛、斜视、吞咽困难和误吸性肺病。脑部磁共振成像显示脑桥有脓肿,遂行显微手术抽脓。术后病程顺利,神经功能完全恢复。临床和影像学检查显示,尽管仍有轻度强化,但4个月后脑桥病变逐渐消退。本病例是文献报道的第18例小儿脑干脓肿。
发病的平均年龄为8.1±4岁(范围0.75 - 16岁),无性别差异。高发病率是其典型特征,主要累及运动功能。最常见的临床体征是颅内压升高、肢体运动功能障碍和脑神经麻痹。18例中有10例(56%)出现发热。3例患者接受了保守治疗。3例患者接受了立体定向抽脓,另外12例接受了显微手术抽脓或切除。自80年代以来未报告死亡病例。然而,发病率仍然很高。
提高功能预后需要高度的临床怀疑指数。立体定向引导或显微手术抽脓仍是良好的治疗选择。小儿脑干脓肿的罕见性以及最佳治疗的必要性使得基于病例的更新非常特殊。