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NEUROLOGY 2007;69:1451-1459
© 2007 American Academy of Neurology

Differences and similarities between atypical facial pain and trigeminal neuropathic pain

Heli Forssell, DDS, PhD, Olli Tenovuo, MD, PhD, Pekka Silvoniemi, MD, PhD and Satu K. Jääskeläinen, MD, PhD

From the Departments of Oral Diseases (H.F.), Neurology (O.T.), Otorhinolaryngology (P.S.), and Clinical Neurophysiology (S.K.J.) and Pain Clinic (H.F.), Turku University Hospital, Finland.

Address correspondence and reprint requests to Dr Jääskeläinen, Department of Clinical Neurophysiology, University Hospital, PL 52, FIN-20521 Turku, Finland

Objective: To investigate contribution of neuropathic mechanisms to clinically diagnosed atypical facial pain (AFP) using neurophysiologic and thermal quantitative sensory testing (QST) and comparing findings in AFP with those in definite trigeminal neuropathic pain (TNP).

Methods: Twenty patients with AFP and 12 patients with TNP participated after thorough clinical diagnostic workup. All patients underwent blink reflex (BR) recordings, habituation of the BR, and (except one patient with TNP) thermal QST. The results were compared with the reference values of our laboratory for normality.

Results: Of the patients with AFP, 75% showed abnormal findings. The BR responses were abnormal in three (15%) AFP patients (in two patients, the findings were compatible with a peripheral neuropathy and in one with a brainstem lesion), and in seven (58%) TNP patients. Seven (35%) patients with AFP and four (33%) with TNP showed increased excitability of the BR in the form of deficient habituation. Thermal QST indicated abnormal small fiber function in 11 (55%) patients with AFP and in all patients with TNP tested. QST showed thermal hypoesthesia in 45% and warm allodynia in 10% of patients with AFP. In TNP, all findings indicated thermal hypoesthesia. Abnormalities in BR and thermal QST were less frequent in AFP than TNP, but when present, type and pattern of findings were similar in both conditions.

Conclusions: Clinical diagnosis of atypical facial pain represents a heterogeneous entity and seems to form a continuum regarding the level and extent of neuropathic involvement. Without detailed neurophysiologic and quantitative sensory examinations, neuropathic cause of chronic orofacial pain may be overlooked.

GLOSSARY: = ß-amyloid protein; AFP = atypical facial pain; BR = blink reflex; CDT = cold detection threshold; HPT = heat pain threshold; QST = quantitative sensory testing; TN = trigeminal nerve; TNP = trigeminal neuropathic pain; WDT = warm detection threshold.


satu.jaaskelainen{at}tyks.fi

Supported by research grants from the Finnish Dental Society, Sigrid Jusélius Foundation, Finnish Medical Foundation, and Turku University Hospital.

Disclosure: The authors report no conflicts of interest.

Received October 25, 2006. Accepted in final form April 20, 2007.




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