Abstract
Caglia et al.from Italy, present a case of 28-year-old female with cutaneous Rosai-Dorfmann disease occurring in a patient with a past medical history of autism spectrum disorders. The purely cutaneous form of the disease is extremely rare, accounting for approximately 3% of cases.
Highlights
Kar et al [3] from India, report a rare case of a 16-year-old girl with a rare site and unusual presentation of neurocystercosis
Open Access was observed after discontinuation of the drug and treatment of methylprednisolone
The diagnosis was based on endemic area for WestNile Virus (WNV), thyroid lobes enlargement, higher serum CRP levels, high IgM antibodies against WNV, normal throid peroxidase level and patient response to corticosteroids
Summary
Kar et al [3] from India, report a rare case of a 16-year-old girl with a rare site and unusual presentation of neurocystercosis. Colson et al [6] from Belgium, report of two patients (a 55-yearold woman, a 42-year-old woman) who developed lymphedema and scleroderma-like skin changes after treatment with Paclitaxel® for breast cancer.
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