Biomedical subjects
L Vaillant
Publications and source records attributed to L Vaillant.
[Late cutaneous porphyria secondary to a primary cancer of the liver].
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[Autoimmune pemphigus combined with alpha 1-antitrypsin deficiency].
It has been demonstrated experimentally that the bullae observed in autoimmune pemphigus are due to the action of proteases. So far, no case of pemphigus associated with deficiency in antiprotease has been reported. We present a case of pemphigus associated with familial deficiency in alpha 1-antitrypsin (alpha 1-AT), a major human body antiprotease. A 35-year old man presented with pemphigus preceded during 18 months, and accompanied by pruritus. The lesions were polymorphous, being made of solitary bullae, circinate vesiculobullae and squamous scabie plaques. Histopathological examination showed an intraepidermal bulla with acantholysis, a very spongiosis. The diagnosis of autoimmune pemphigus was confirmed by fluorescence of the epidermis in IgG and C3 and by the presence of antibodies directed against the intracellular substance. The initial treatment, which consisted of prednisolone 10 mg/kg/day and 10 plasma exchanges, was rapidly successful, but several relapses occurred thereafter. Two years after the pemphigus was diagnosed, a panlobular emphysema was discovered which made it possible to demonstrate a severe familial deficiency in alpha 1-AT of the Pi phenotype. This is the first published case of alpha 1-AT deficiency associated with autoimmune pemphigus. In our patient the skin disease presented as herpetiform pemphigus (initial features of dermatitis herpetiformis, followed by misleading polymorphous lesions, rare acantholytic cells, good response to corticosteroids), but there was no eosinophilic spongiosis. The frequency of alpha1-AT deficiency (estimated at 1 in 1,000 in northern Europe) and the lack of published cases with such an association may suggest a pure coincidence.(ABSTRACT TRUNCATED AT 250 WORDS)
[What is the cause of acquired ciliary hypertrichosis in AIDS?].
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[Cutaneous Alternaria tenuissima alternariosis].
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[The elimination of dental and sinusal infectious foci in dermatologic pathology. A double-blind study in 27 cases confined to chronic urticaria].
The authors study the responsibility on dental and sinusal focal sepsis in the evolution of chronic urticaria. The conclusion is that the eradication of dental and sinusal focal sepsis doesn't significantly change the evolution of chronic urticaria (Student Fischer test).
[Multiple cutaneous and hepatic angioma in a newborn infant].
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Multiple cutaneous hemangiomas and coarctation of the aorta with right aortic arch.
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Erythromycin ethyl succinate: diffusion through interstitial dermal fluid.
Erythromycin is widely used in dermatology. There are few studies of its diffusion in the skin. The diffusion of erythromycin ethyl succinate (EES) in dermal fluid has now been investigated by the suction blister method. Suction blister fluid (SBF) and blood samples were collected from 10 volunteers before administration of 1 g EES and 10 times during the following 24 h. The median peak serum level was 2.05 micrograms/ml and in SBF it was 0.34 microgram/ml. The median ratio of the areas under curves (f SBF/f serum) was 43%. In all subjects EES concentrations in SBF between the second and twelfth hours exceeded 0.1 g/ml. The results show good diffusion of EES through normal skin from the second to the twelfth hours after oral administration.
[Behçet's disease with myositis].
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[Leg ulcer of the pyoderma gangrenosum type. Manifestation of tertiary cutaneous syphilis].
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[Annular cutaneous sarcoidosis of the forehead: treatment with isotretinoin].
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[Tuberculous abscess of the psoas muscle manifested through a mass in the thigh].
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[Gardner-Diamond syndrome in a 14-year-old girl. Discussion on the diagnostic value of skin tests].
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[Isoxicam reaction of the ectodermosis erosiva pluri-orificialis type].
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[Behçet's disease with predominantly digestive manifestations].
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[Extraoral oriented forces].
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