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NEUROLOGY 2006;66:499-504
© 2006 American Academy of Neurology

Small vessel abnormalities in alternating hemiplegia of childhood

Pathophysiologic implications S. Auvin, MD, S. Joriot-Chekaf, MD, J. C. Cuvellier, MD, F. Pandit, PhD, J. M. Cuisset, MD, M. M. Ruchoux, MD, PhD* and L. Vallée, MD*

From the Departments of Pediatric Neurology (S.A., S.J.-C., J.C.C., F.P., J.M.C., L.V.) and Neuropathology (M.M.R.), University Hospital, Lille, France.

Address correspondence and reprint requests to Dr. S. Auvin, Service de Neurologie pédiatrique, Hôpital Roger Salengro, Boulevard du Pr J Leclercq, 59037 Lille Cedex, France; e-mail: auvin{at}invivo.edu

Background: The pathophysiology of alternating hemiplegia of childhood (AHC) is unclear. The authors evaluated the skin and muscle biopsies from patients with AHC for vascular abnormalities.

Methods: Skin biopsy specimens from four patients ages 18 months, 8 years, 9 years, and 18 years and muscle biopsies from two of these patients were examined by electron microscopy and compared with healthy controls.

Results: Vascular abnormalities were found in both skin and muscle. Skin biopsies showed similar abnormalities in all four patients. Vacuoles were visible in the endothelium. The most striking abnormality was the presence in the tunica media of small and unevenly shaped vascular smooth muscle cells (VSMCs) containing intracytoplasmic vacuoles and, occasionally, apoptotic nuclei, with variations according to patient age. Moreover, most VSMCs had lost junctions with neighboring cells, and some were completely isolated. In vessels from muscle biopsies, the VSMCs showed vacuoles, residual osmiophilic deposits, and myofilament loss with substitution by vacuoles.

Conclusions: The vascular abnormalities in our patients suggest a primary or secondary vascular pathophysiology to alternating hemiplegia of childhood. The vascular smooth muscle cells may be the initial target of the disease process.

* These authors contributed equally to this work.

Disclosure: The authors report no conflicts of interest.

Received March 30, 2005.

Accepted in final form October 31, 2005.




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[Abstract] [Full Text] [PDF]