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DOI 10.1097/cnd.0b013e318209efb1

Медицинская библиотека · Journal of clinical neuromuscular disease · 2011

Comparison of sudomotor and sensory nerve testing in painful sensory neuropathies.

Killian James M, Smyth Shane, Guerra Rudy, Adhikari Ishan, Harati Yadollah

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Аннотация

OBJECTIVE

To compare results of quantitative sudomotor axon reflex testing (QSART), dorsal sural, and sural sensory nerve testing in patients with painful sensory neuropathy (PSN).

METHODS

Fifty-six patients with symptoms and neurologic examinations consistent with PSN who had both autonomic and nerve conduction studies were identified from 376 patients with a clinical diagnosis of painful neuropathy. Cases were clinically categorized as large-fiber or small-fiber neuropathies by described criteria. The results of sural, dorsal sural, and QSART tests were then analyzed in relationship to these two clinical groups.

RESULTS

Evidence of unmyelinated fiber abnormalities by QSART was noted in 85% of clinical large-fiber and 69% of clinical small-fiber groups. Dorsal sural potentials were absent in all the large-fiber group but also in 52% of clinically classified small-fiber neuropathies. When QSART and dorsal sural abnormalities were combined, the identification of abnormalities in all the cases of PSN was 89% with 75% of cases (42) showing mixed large and small fiber abnormalities, 14% unmyelinated sensory fiber abnormalities (by QSART), and 11% normal studies.

CONCLUSION

This study demonstrates the value of combining both QSART and dorsal sural sensory testing in verifying the diagnosis of PSN. The majority of cases demonstrate involvement of unmyelinated C fibers as well as large/medium myelinated fibers, thereby separating mixed large- and small-fiber sensory neuropathies from those cases classified by clinical criteria solely as small-fiber neuropathy.

Для цитирования: Killian James M, Smyth Shane, Guerra Rudy, Adhikari Ishan, Harati Yadollah. Comparison of sudomotor and sensory nerve testing in painful sensory neuropathies.. Journal of clinical neuromuscular disease. 2011. DOI: 10.1097/cnd.0b013e318209efb1.

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