Results 121 to 130 of about 119,526 (169)
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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.
P Merlob, B Hazaz, S H Reisner
exaly +3 more sources
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.
P Merlob, B Hazaz, S H Reisner
exaly +3 more sources
The Journal of the American Dental Association, 1980
Pemphigus vulgaris is a rare, potentially fatal skin disease with lesions usually first appearing in the mouth. Histologic examination is the only reliable mechanism with which to establish an accurate diagnosis. An elderly patient with multiple oral and skin lesions was diagnosed, referred to the dermatology service, and successfully treated with ...
P L, Kempler, T R, Schott
openaire +2 more sources
Pemphigus vulgaris is a rare, potentially fatal skin disease with lesions usually first appearing in the mouth. Histologic examination is the only reliable mechanism with which to establish an accurate diagnosis. An elderly patient with multiple oral and skin lesions was diagnosed, referred to the dermatology service, and successfully treated with ...
P L, Kempler, T R, Schott
openaire +2 more sources
Pemphigus Vulgaris and Paraneoplastic Pemphigus
Oral and Maxillofacial Surgery Clinics of North America, 2008The history, epidemiology, pathophysiology, clinical presentation, diagnostic work-up, histopathology, and treatment of PV and PNP have been presented. These life-threatening, autoimmune, mucocutaneous bullous conditions may be encountered first by oral health providers and, therefore, deserve keen understanding and attention by the oral and ...
Wendell A, Edgin +2 more
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The immunogenetics of pemphigus vulgaris
Autoimmunity Reviews, 2005Pemphigus vulgaris (PV) is an autoimmune blistering disease of the skin of unknown etiology. While various environmental factors have been implicated as triggering agents, HLA association is probably the most important predisposing factor. The aim of this review is to highlight the association of HLA with pemphigus vulgaris.
Ron Loewenthal
exaly +3 more sources
Interventions for pemphigus vulgaris and pemphigus foliaceus
Cochrane Database of Systematic Reviews, 2009A range of interventions have been described for treatment of pemphigus, however the optimal therapeutic strategy has not been established.To assess the efficacy and safety of all interventions used in the management of pemphigus vulgaris and pemphigus foliaceus.We searched the Cochrane Skin Group Specialised Register (October 2008), The Cochrane ...
Linda K Martin +5 more
openaire +2 more sources
Acta Paediatrica, 1991
ABSTRACT. Pemphigus vulgaris is extremely rare in childhood. Only 35 cases of juvenile pemphigus vulgaris have been reported in the literature up until to now. During the pre‐steroid era, the outcome of the disease was usually regarded as fatal. Today, the prognosis has improved because of the possibility of early diagnosis by immunoflourescent ...
V, Graff-Lonnevig, T, Kaaman
openaire +2 more sources
ABSTRACT. Pemphigus vulgaris is extremely rare in childhood. Only 35 cases of juvenile pemphigus vulgaris have been reported in the literature up until to now. During the pre‐steroid era, the outcome of the disease was usually regarded as fatal. Today, the prognosis has improved because of the possibility of early diagnosis by immunoflourescent ...
V, Graff-Lonnevig, T, Kaaman
openaire +2 more sources
Dermatologica, 2009
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 ...
V, Katzenelson +5 more
openaire +4 more sources
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 ...
V, Katzenelson +5 more
openaire +4 more sources
Pemphigus vulgaris and malignancy
International Journal of Oral Surgery, 1985A case of oral squamous cell carcinoma with pemphigus vulgaris is reported and the literature is reviewed. Association between the above entities has essentially been founded upon the specificity of cancer-associated antigen. To date, such an antigen has not been adequately defined, and, therefore, any causal relationship between the 2 processes on the
A, Armin, H, Nadimi, J, Robinson
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Journal of the American Academy of Dermatology, 1982
An infant was born with bullous lesions. The mother had had pemphigus vegetans diagnosed 1 year earlier, with remission during pregnancy. Histopathology and immunofluorescence of the infant's lesions were consistent with pemphigus vulgaris. The mother and infant had low titers of epidermal intercellular antibodies in their sera.
J S, Storer +3 more
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An infant was born with bullous lesions. The mother had had pemphigus vegetans diagnosed 1 year earlier, with remission during pregnancy. Histopathology and immunofluorescence of the infant's lesions were consistent with pemphigus vulgaris. The mother and infant had low titers of epidermal intercellular antibodies in their sera.
J S, Storer +3 more
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The Journal of Dermatology, 1985
ABSTRACTA 32‐year‐old Japanese man was seen because of a crusted and oozing plaque on his scalp of 3 years' duration. Histologically, suprabasal clefts and bullae containing acantholytic cells as well as intercellular IgG and C3 deposits were found by the direct immunofluorescent technique. There were no circulating pemphigus antibodies. The lesion was
A, Yagi, S, Shiraishi, Y, Miki
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ABSTRACTA 32‐year‐old Japanese man was seen because of a crusted and oozing plaque on his scalp of 3 years' duration. Histologically, suprabasal clefts and bullae containing acantholytic cells as well as intercellular IgG and C3 deposits were found by the direct immunofluorescent technique. There were no circulating pemphigus antibodies. The lesion was
A, Yagi, S, Shiraishi, Y, Miki
openaire +2 more sources