Livedo reticularis is a spastic-anatomical condition of the small vessels which
translates morphologically by a reticular pattern, interspersing cyanosis, pallor and
erythema. The same can be congenital or acquired. Among the acquired, we highlight
the physiological livedo reticularis and the idiopathic livedo by vasospasm; the
latter configures the most common cause. The drug-induced type is less common. The
drugs amantadine and norepinephrine are often implicated. Cyanosis is usually
reversible if the causative factor is removed, however, with chronicity, the vessels
may become permanently dilated and telangiectatic. We report a case of a patient
diagnosed with Parkinson’s disease with chronic livedo reticularis associated with
the use of amantadine and improvement after discontinuation of the drug.
Myotonic dystrophy (MD) is a neuromuscular disease with myotonia, progressive weakness, and involvement of CNS, heart, and gastrointestinal system. Excessive daytime sleepiness (EDS) in myotonic dystrophy type 1 (MD1) is related to sleep breathing diseases, restless leg syndrome, periodic limb movements during sleep and narcoleptic-like phenotype. However, authors highlight a central dysfunction of sleep regulation. We describe a 26-year-old, female, MD1 patient with EDS. Sleep diary/actigraphy evidenced two different circadian periods with values of 1442 and 1522 min. Agomelatine, 50 mg at night, was prescribed with improvement of the circadian rhythm and complaints of sleepiness. The identification of unanticipated causes of EDS, such as circadian rhythm disorders permits an appropriated treatment. As we know, it is the first relate of non-24-h sleep-wake disorder in patient with MD1. Sleep diary and actigraphy could be good options to investigate sleep-wake cycle disorder in patients with MD and EDS.
Homem de 44 anos com inchaço indolor progressivo no topo da cabeça nos últimos 10 meses com dor de cabeça. O exame físico revelou aproximadamente 4 por 5 cm de edema, consistência firme.
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