Results 261 to 270 of about 161,137 (307)
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Dermatology, 1990
Familial pemphigus vulgaris was found in a Jewish woman and her son who developed the disease within a period of 18 months from one another. HLA typing was performed in the mother and son as well as in the unaffected father and sister. Examination of the HLA antigens in this family indicates that there may be different variants of DR4, DQw3 and that ...
Carlos Idises +5 more
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Familial pemphigus vulgaris was found in a Jewish woman and her son who developed the disease within a period of 18 months from one another. HLA typing was performed in the mother and son as well as in the unaffected father and sister. Examination of the HLA antigens in this family indicates that there may be different variants of DR4, DQw3 and that ...
Carlos Idises +5 more
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Dermatology, 1985
A case of familial pemphigus vulgaris is described in an uncle and his niece who developed the disease 18 years apart. The man died from pemphigus in 1964. The diagnosis was confirmed histopathologically in both cases, but immunofluorescent microscopic studies were performed only in the woman because the technique was not available in 1964.
M. Himelfarb, B. Dorfman, S. Brenner
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A case of familial pemphigus vulgaris is described in an uncle and his niece who developed the disease 18 years apart. The man died from pemphigus in 1964. The diagnosis was confirmed histopathologically in both cases, but immunofluorescent microscopic studies were performed only in the woman because the technique was not available in 1964.
M. Himelfarb, B. Dorfman, S. Brenner
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Pemphigus Vulgaris and Pregnancy
Obstetrical & Gynecological Survey, 1995Pemphigus vulgaris (PV), an autoimmune bullous dermatosis, is rarely encountered in pregnancy. Two women with PV and their three pregnancies are described. Pregnancy outcome was generally good, although one of the neonates had characteristic PV skin lesions that resolved spontaneously. The pathophysiology, clinical manifestations, and special issues of
G. Ohel +3 more
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Journal of the European Academy of Dermatology and Venereology, 2008
AbstractBackground Pemphigus vulgaris can be divided into mucosal, mucocutaneous and cutaneous subtypes. A higher mortality rate has been shown with mucocutaneous involvement.Objectives The aim of this retrospective study was to analyse the association of clinical subtypes of pemphigus vulgaris with remission rates.Patients/methods One hundred ...
R Abedini +5 more
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AbstractBackground Pemphigus vulgaris can be divided into mucosal, mucocutaneous and cutaneous subtypes. A higher mortality rate has been shown with mucocutaneous involvement.Objectives The aim of this retrospective study was to analyse the association of clinical subtypes of pemphigus vulgaris with remission rates.Patients/methods One hundred ...
R Abedini +5 more
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Pemphigus: Pemphigus vulgaris and pemphigus foliaceus
1990The term pemphigus stems from the Greek pemphix (blister) [1] and describes a group of chronic blistering skin diseases in which autoantibodies are directed against the cell surface of keratinocytes, resulting in the loss of cohesion between epidermal cells, through a process called acantholysis. Pemphigus is divided into pemphigus vulgaris (PV) with a
John R. Stanley, Stephan Müller
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Pemphigus Vulgaris in Childhood
Archives of Pediatrics & Adolescent Medicine, 1972Pemphigus vulgaris rarely occurs in children. We present the youngest reported case. All six cases of childhood pemphigus vulgaris proven by biopsy began with lesions confined to the oral mucosa. In each case diagnosis was delayed until the more typical cutaneous lesions began to appear.
E. Richard Harrell, Patrick J. Murphy
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Pediatrics, 1986
The case history of a baby with neonatal pemphigus vulgaris is presented. This is the 13th case of pemphigus vulgaris during pregnancy reported in the literature. The correlations between the clinical, histologic, and immunofluorescent findings are discussed and a review of all previously reported cases is presented.
H. Rogovin +4 more
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The case history of a baby with neonatal pemphigus vulgaris is presented. This is the 13th case of pemphigus vulgaris during pregnancy reported in the literature. The correlations between the clinical, histologic, and immunofluorescent findings are discussed and a review of all previously reported cases is presented.
H. Rogovin +4 more
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Oral Surgery, Oral Medicine, Oral Pathology, 1981
Abstract Although pemphigus vulgaris is uncommon in adolescence, its occurrence in two patients in this age group is reported. In both cases the lesions were confined to the oral mucosa and the diagnosis was established by the typical histologic picture and positive direct and indirect immunofluorescence.
Alexandra Sklavounou +2 more
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Abstract Although pemphigus vulgaris is uncommon in adolescence, its occurrence in two patients in this age group is reported. In both cases the lesions were confined to the oral mucosa and the diagnosis was established by the typical histologic picture and positive direct and indirect immunofluorescence.
Alexandra Sklavounou +2 more
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Archives of Dermatology, 1952
IT IS DIFFICULT, as Michelson 1 states, to draw a sharp line of distinction between acute and chronic pemphigus vulgaris, and consequently there may be some overlapping in our presentations. As I have looked over some of the literature dealing with pemphigus, I have been struck with the fact that, while much investigative work has been done, one finds
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IT IS DIFFICULT, as Michelson 1 states, to draw a sharp line of distinction between acute and chronic pemphigus vulgaris, and consequently there may be some overlapping in our presentations. As I have looked over some of the literature dealing with pemphigus, I have been struck with the fact that, while much investigative work has been done, one finds
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The Journal of Dermatology, 2008
ABSTRACTA male newborn with skin erosions was born to a 32‐year‐old woman who was under treatment for pemphigus vulgaris that had been diagnosed 16 months earlier. Antibodies to desmoglein (Dsg)1 and Dsg3 were analyzed by enzyme‐linked immunosorbent assay. Index values of antibodies to Dsg1 and Dsg3 were 49 (normal index values, <14) and 121 (normal
Yoshiko Mine +8 more
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ABSTRACTA male newborn with skin erosions was born to a 32‐year‐old woman who was under treatment for pemphigus vulgaris that had been diagnosed 16 months earlier. Antibodies to desmoglein (Dsg)1 and Dsg3 were analyzed by enzyme‐linked immunosorbent assay. Index values of antibodies to Dsg1 and Dsg3 were 49 (normal index values, <14) and 121 (normal
Yoshiko Mine +8 more
openaire +3 more sources