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[St. John's wort (Hypericum perforatum L.). A plant with relevance for dermatology].

Saint John's wort (Hypericum perforatum L.) is a herbal remedy that is effective in the treatment of mild to moderate depression. In traditional folk medicine, oily extracts of St. John's wort are used for topical treatment of wounds, burns and myalgia. The lipophilic phloroglucin-derivative hyperforin has antibacterial and antiinflammatory effects. These effects could be of relevance in topical treatment of infected wounds and other dermatoses, but no studies have been conducted so far. The naphtodianthrone hypericin is a photodtodynamic active substance that kills tumor cells via the induction of apoptosis. Hypericin also displays antiviral activity in vitro. In vivo, intravenous or oral treatment with hypericin of HIV-infected subjects did not result in a reduction of the virus load. Most of the patients treated with hypericin experienced phototoxicity. Similar phototoxic symptoms ("hypericism") have been observed in grazing animals ingesting large amounts of St. John's wort. In contrast, antidepressant medication with St. John's wort usually does not produce phototoxic symptoms. Recent pharmacokinetic studies suggest that the phototoxic threshold level of hypericin is not reached with dosages used for the oral treatment of depression. However, very recent reports demonstrated interactions of St. John's wort with other drugs such as digoxin, indinavir and cyclosporin. Blood levels of these drugs were dramatically decreased by St. John's wort. This should be considered in the treatment of skin conditions with antiviral drugs or cyclosporin.

Depressive Disorder↗

[Photodermatosis and photoprotection in children].

Photodermatosis is an heterogeneous group of affections characterized by an abnormal sensitivity of skin to sunlight responsible of a local or generalized eruption. Rare in children, the most frequent of them such as sun-burns, phytophotodermatosis and phototoxicity are fortunately benign, brief and spontaneously resolving. Some of them disappear spontaneously after few years like polymorphic light eruptions which are rather observed in children older than ten years. In case of recurrence, rare diagnosis have to be investigated with specific tests (phototests, blood exams, genetic investigations) as some metabolic or genetic disorders may be revealed by a photosensitivity, especially before the age of three years. The questioning of the parents and of the child is fundamental. Many diagnosis may be discussed depending on age and circumstances. Treatment consists in photoprotection recommendations, solar eviction and regular application of protective screens, whose spectrum of protection are different and have to be known in order to prescribe an adapted photoprotection.

Age Factors↗

Photophobia and autonomic responses to facial pain in migraine.

Subjective and autonomic responses to visual stimulation and facial pain were investigated in 10 migraine sufferers and 21 'non-headache' control subjects. Ratings of glare- and light-induced pain were greater in migraine sufferers than control subjects. In migraine sufferers, glare ratings increased during painful mechanical stimulation of the nasal ala, the side of the nose and the back of the neck. Glare ratings decreased in both groups during painful stimulation of the chin. Light-induced pain increased during painful stimulation of all four sites in migraine sufferers, but not control subjects. Increases in forehead pulse amplitude during painful mechanical stimulation were greater bilaterally in migraine sufferers than in control subjects, consistent with loss of inhibitory influences on vascular reactions in the face. Visual stimulation facilitated lacrimation when the nasal ala was pinched, but visual stimulation coupled with pain elsewhere in the head and neck did not. The lacrimal response to combined nasal ala and visual stimulation was absent on the symptomatic side in patients with unilateral headache, indicating local parasympathetic deficit in migraine. These findings suggest that migraine is associated with loss of inhibitory subcortical processes which normally suppress sensations of glare and light-induced pain, and which may also suppress vasodilator responses to facial pain. Loss of inhibitory pain-control mechanisms could interact in a vicious circle with autonomic disturbances during migraine.

Adolescent↗

Solar eczema.

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Dermatitis, Phototoxic↗