Peripheral neuropathy in acrodermatitis chronica atrophicans - a late Borrelia manifestation
Corresponding Author
E. Kindstrand
Karolinska Institute, Departments of Neurology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Eva Kindstrand, Karolinska Institute, Dept of Neurology, Huddinge University Hospital, S-141 86 Huddinge, SwedenSearch for more papers by this authorB. Y. Nilsson
Neurophysiology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorA. Hovmark
Dermatology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorR. Pirskanen
Karolinska Institute, Departments of Neurology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorE. Asbrink
Dermatology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorCorresponding Author
E. Kindstrand
Karolinska Institute, Departments of Neurology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Eva Kindstrand, Karolinska Institute, Dept of Neurology, Huddinge University Hospital, S-141 86 Huddinge, SwedenSearch for more papers by this authorB. Y. Nilsson
Neurophysiology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorA. Hovmark
Dermatology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorR. Pirskanen
Karolinska Institute, Departments of Neurology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorE. Asbrink
Dermatology, Stockholm Sorter Hospital, S-118 83 Stockholm, Sweden
Search for more papers by this authorAbstract
Clinical and/or neurophysiological signs of peripheral neuropathy were found in 64% of 63 consecutive untreated patients with the late borrelial manifestation acrodermatitis chronica atrophicans (ACA). The neuropathy frequency was significantly higher in the patients than in 30 age- and sex-matched control persons of whom 27% had neuropathy findings. The most common neuropathy in ACA was a symmetric distal sensory polyneuropathy. In a subgroup of patients with localized or asymmetric neuropathy, the changes were found more often in extremities with than without visible ACA lesions. Neuropathy symptoms, most often pain and/or paresthesia, were present in 64% of the patients, compared to in 13% of the control persons. Thus, both symptoms and signs of neuropathy were significantly more frequent in patients with untreated ACA than in control subjects.
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