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Biomedical subjects

L Jacquelin

Publications and source records attributed to L Jacquelin.

5 recordsLinked to original sources

[Schnitzler's syndrome. A new case].

A new case of Schnitzler's syndrome is reported in a 72-year old man hospitalized for severe deterioration of his general condition associated with recurrent ancient urticaria. Paraclinical examinations, which showed inflammatory syndrome, bone condensation and IgM monoclonal gammapathy, led to the diagnosis of Schnitzler's syndrome, first described in 1972. Twenty-two cases have now been published, characterized by vasculitic urticaria, osteosclerosis and IgM macroglobulinaemia. There is also severe inflammatory syndrome and the other immunological examinations are normal. Recent studies suggest the possibility of uncontrolled activity of interleukin-1 alpha. The condition is chronic and usually benign, but the fear of malignant transformation in the long term makes the therapeutic choice difficult.

Aged↗

Acute generalized exanthematous pustular dermatitis and viral infection.

Three patients with acute generalized exanthematous pustular dermatitis (AGEPD) are presented. This new clinical entity comprises generalized erythema, erythema multiforme, amicrobial pustules, fever and spontaneous healing over a 10-day period. Histologically, there are a mixed neutrophilic and eosinophilic vasculitis and an eosinophilic subcorneal and spongiform pustule. All the patients experienced pharyngitis 1 week before the onset of the rash. Two of them had high-titered IgM-neutralizing antibodies to enteroviruses and 1 had an enterovirus in stool and urine. AGEPD may be related to a viral infection and may occur in patients with a genetic predisposition to psoriasis. The diagnosis of AGEPD should be made early enough so that the patients are not given the often aggressive therapy of pustular psoriasis.

Adolescent↗

Chronic bullous dermatosis of childhood. Immunological and ultrastructural studies on the melanocyte--dermal junction.

Ultrastructural study of a case of benign chronic bullous dermatosis of childhood revealed the presence of melanocytes in the base of the blister. The melanocyte anchorage mechanism is described. The absence of labelling by bullous pemphigoid antibodies on the base of the blister, where melanocytes persist, indicates that the antigens recognized by these autoantibodies do not exist in the melanocyte basal membrane-contact zones. This suggests that the chemical nature of the melanocyte dermal junction anchorage system is different from that of the hemidesmosomes.

Antigens↗