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Restrepo, Carlos E.

Mayo Clinic

Instituto Neurológico de Colombia

Citations 3

The almost-invisible perineurioma
Restrepo, Carlos E., Amrami, Kimberly K. , Howe, Benjamin M. , Dyck, P. James B. , Mauermann, Michelle L. , Spinner, Robert J. , Mauermann, Michelle L

Neurosurgical Focus | September 1, 2015 | Volume: 39 | Issue: 3 | Pages: E13

10.3171/2015.6.focus15225 Get It

Intraneural perineurioma is a rare, benign slow-growing lesion arising from the perineurial cells that surrounds the peripheral nerve fibers. Typically it presents during childhood and young adulthood as a motor mononeuropathy. MRI plays an essential role in the diagnosis and localization of the lesion, which appears as a fusiform enlargement of the nerve fascicles that enhances intensely with gadolinium. Despite the typical clinical and radiological features, intraneural perineurioma remains largely underdiagnosed because of the lack of familiarity with this entity, but also as a result of technical limitations with conventional MRI that is typically performed as a screening test over a large field of view and without contrast sequences. The purpose of this article is to present the pitfalls and pearls learned from years of experience in the diagnosis and management of this relatively rare condition. Clinical suspicion and detailed neurological examination followed by high-quality electrophysiological studies (EPS) must lead to an adequate preimaging localization of the lesion and narrowing of the imaging area. The use of high-resolution (3-T) MRI combined with gadolinium administration will allow adequate visualization of the internal anatomy of the nerve and help in differentiating other causes of neuropathy. In cases where the lesion is not recognized but clinical suspicion is high, possible errors must be assessed, including the EPS localization, area of imaging, MRI resolution, and slice thickness.
Perineural spread of malignant melanoma from the mandible to the brachial plexus: case report
Restrepo, Carlos E., Spinner, Robert J. , Howe, B. Matthew, Jentoft, Mark E. , Markovic, Svetomir N. , Lachance, Daniel Honore

Journal of Neurosurgery | January 23, 2015 | Volume: 122 | Issue: 4 | Pages: 784-790

10.3171/2014.12.jns14852 Get It

Perineural spread is a well-known mechanism of dissemination of head and neck malignancies. There are few reports of melanoma involving the brachial plexus in the literature. To their knowledge, the authors report the first known case of perineural spread of malignant melanoma to the brachial plexus. Clinicoradiological and anatomopathological correlation is presented, highlighting the importance of peripheral nerve communications in perineural spread.
Expanding what is known of the anatomy of the spinal accessory nerve
Restrepo, Carlos E., Tubbs, R. Shane , Spinner, Robert J.

Clinical Anatomy | December 29, 2014 | Volume: 28 | Issue: 4 | Pages: 467-471

10.1002/ca.22492 Get It

The spinal accessory nerve (SAN) is classically considered a motor nerve innervating the sternocleidomastoid and trapezius muscles. Its anatomical relevance derives from the high prevalence of lesions following head and neck surgeries. As expected, trapezius weakness and atrophy are the most common findings; however, it is also commonly accompanied by pain and other sensory deficits that have no clear explanation, suggesting other functions. We have recently seen two patients presenting with an unrecognized sign, that is, subclavicular/pectoral asymmetry secondary to the SAN lesion. Retrospectively, we reviewed other patients with similar findings in our case series and in the literature. We discuss the anatomical connections of the SAN with the superficial cervical plexus and propose an explanation for this finding. Of the 41 patients in our series, we identified this sign in all who had preoperative photographs. New insights on the anatomy and connections of the SAN may account for the diversity of symptoms and signs presented following an operative intervention as well as the variability of its severity. Clin. Anat. 28:467–471, 2015. © 2014 Wiley Periodicals, Inc.