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1.
Rev Stomatol Chir Maxillofac Chir Orale ; 117(5): 351-356, 2016 Nov.
Article in English | MEDLINE | ID: mdl-27473929

ABSTRACT

INTRODUCTION: Dislocation of the mandibular condyle into the middle cranial fossa after a trauma is a rare event. The lack of appropriate treatment can lead to ankylosis of the temporomandibular joint (TMJ). We report about a case of TMJ ankylosis following intracranial dislocation of the mandibular condyle through the roof of the articular fossa. CASE REPORT: A 9-year-old patient was referred for a severe limitation of mouth opening that began progressively one year before. A history of chin injury due to an accidental fall was found. Preoperative CT scan showed a TMJ ankylosis on the right side combined with a dislocation of the mandibular condyle into the middle cranial fossa. Treatment consisted in an intracranial resection of the mandibular condyle, partial removal of the ankylosis block and TMJ arthroplasty. DISCUSSION: Our case is the second case of TMJ ankylosis following intracranial dislocation of the mandibular condyle and treated with arthroplasty alone published in the English literature. There is no consensus regarding the pathophysiology of TMJ ankylosis and regarding the attitude towards the ankylosis block. In our case, no recurrence was noticed after a one-year follow-up. An interdisciplinary approach is needed, including maxillofacial surgeon, neurosurgeon, physiotherapist and orthodontist.


Subject(s)
Ankylosis/pathology , Cranial Fossa, Middle/pathology , Joint Dislocations/pathology , Mandibular Condyle/pathology , Temporomandibular Joint Disorders/pathology , Temporomandibular Joint/pathology , Accidental Falls , Ankylosis/etiology , Ankylosis/surgery , Child , Cranial Fossa, Middle/surgery , Humans , Joint Dislocations/etiology , Joint Dislocations/surgery , Male , Mandibular Condyle/surgery , Temporomandibular Joint/surgery , Temporomandibular Joint Disorders/etiology , Temporomandibular Joint Disorders/surgery
2.
Neurochirurgie ; 48(6): 516-21, 2002 Dec.
Article in French | MEDLINE | ID: mdl-12595808

ABSTRACT

Nocardia spp. cerebral abscesses are rare and usually occur in immunocompromised patients. We report two recent cases of cerebral abscesses due to Nocardia farcinica in immunocompetent patients and review the literature about diagnosis and therapeutic issues. Outcome was good for the two patients following an early identification of the bacteria. Stereotactic biopsy was performed in one case and craniotomy with excision of the abscess in the other case. In both cases, complete identification of the bacteria could be achieved, followed by prolonged antibiotic therapy. Exposure to the germ (mainly telluric) is often difficult to suspect from the past medical history of the patient. Diagnosis is also unexpected. Despite the typically and characteristic aspect on CT and MRI, specific identification and anti-microbial sensitivity profiles are necessary to optimize treatment. In some rare cases, unusual species like Nocardia farcinica, can be resistant to numerous antibiotics requiring adjustments of medical management. Early identification of the bacteria is necessary to achieve good outcome in immunocompetents patients.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Brain Abscess , Nocardia Infections/drug therapy , Nocardia Infections/microbiology , Adult , Brain Abscess/diagnosis , Brain Abscess/microbiology , Brain Abscess/therapy , Humans , Magnetic Resonance Imaging , Male , Middle Aged , Neurosurgical Procedures/methods , Severity of Illness Index , Tomography, X-Ray Computed , Treatment Outcome
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