Persistent idiopathic facial pain

被引:87
作者
Benoliel, Rafael [1 ]
Gaul, Charly [2 ]
机构
[1] Rutgers Sch Dent Med, 110 Bergen St, Newark, NJ 07101 USA
[2] Migraine & Headache Clin Konigstein, Konigstein Im Taunus, Germany
关键词
IFP; daily pain; trigeminal neuralgia; CHRONIC OROFACIAL PAIN; ATYPICAL ODONTALGIA; TRIGEMINAL NEURALGIA; NERVE INJURY; INTERNATIONAL CLASSIFICATION; SOMATOSENSORY ABNORMALITIES; ELECTROPHYSIOLOGIC TESTS; ENDODONTIC TREATMENT; CLINICAL-FEATURES; CLUSTER HEADACHE;
D O I
10.1177/0333102417706349
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Background: Persistent idiopathic facial pain (PIFP) is a chronic disorder recurring daily for more than two hours per day over more than three months, in the absence of clinical neurological deficit. PIFP is the current terminology for Atypical Facial Pain and is characterized by daily or near daily pain that is initially confined but may subsequently spread. Pain cannot be attributed to any pathological process, although traumatic neuropathic mechanisms are suspected. When present intraorally, PIFP has been termed 'Atypical Odontalgia', and this entity is discussed in a separate article in this special issue. PIFP is often a difficult but important differential diagnosis among chronic facial pain syndromes. Aim: To summarize current knowledge on diagnostic criteria, differential diagnosis, pathophysiology and management of PIFP. Methods: We present a narrative review reporting current literature and personal experience. Additionally, we discuss and differentiate the common differential diagnoses associated with PIFP including traumatic trigeminal neuropathies, regional myofascial pain, atypical neurovascular pains and atypical trigeminal neuropathic pains. Results and conclusion: The underlying pathophysiology in PIFP is still enigmatic, however neuropathic mechanisms may be relevant. PIFP needs interdisciplinary collaboration to rule out and manage secondary causes, psychiatric comorbidities and other facial pain syndromes, particularly trigeminal neuralgia. Burden of disease and psychiatric comorbidity screening is recommended at an early stage of disease, and should be addressed in the management plan. Future research is needed to establish clear diagnostic criteria and treatment strategies based on clinical findings and individual pathophysiology.
引用
收藏
页码:680 / 691
页数:12
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