Literature DB >> 12482043

Pemphigus vulgaris: a review of treatment over a 19-year period.

S Ljubojević1, J Lipozencić, S Brenner, D Budimcić.   

Abstract

BACKGROUND: Pemphigus vulgaris is an autoimmune blistering disease of the skin and mucous membranes with a high mortality if left untreated.
OBJECTIVE: We present a retrospective analysis of 159 patients with pemphigus vulgaris and pemphigus vegetans who were admitted to the Department of Dermatology and Venereology, Zagreb University Hospital Center (Zagreb, Croatia) from 1980 to 1998.
RESULTS: Female to male ratio was approximately 2:1. The mean age was 53 years. During the war years in Croatia (1991-95) we noticed a low incidence of pemphigus vulgaris, and from 1996 to 1998 the incidence almost doubled. Diagnosis was based on histopathology [showing typical pemphigus vulgaris changes in 156 (98%) patients], indirect immunofluorescence [positive in 122 (77%) patients], direct immunofluorescence [positive in 141 (89%) patients], and blister smear cytology (Tzanck test) [positive in 115 (72%) patients]. High dosages of prednisone (100-150 mg) were given to 129 patients, which was combined with azathioprine. Patients with refractory pemphigus vulgaris were treated with intramuscular gold (14 patients) and plasmapheresis (five patients). All patients were treated with local ointments. The prolonged use of high doses of corticosteroids and immunosuppressants caused several complications, in particular, steroid diabetes (37 patients), skin infections (26 patients), arterial hypertension (23 patients), cardiorespiratory diseases (22 patients), sepsis (nine patients), etc. During the hospital treatment, 14 patients died, 10 during 1980-89 and only four during the 1990-98 period. The main causes of death were cardiorespiratory failure (six patients) and sepsis (five patients).
CONCLUSIONS: Although pemphigus vulgaris is still a life-threatening disease, today it can be successfully treated with a combination of immunosuppressive agents. Early diagnosis and treatment of pemphigus vulgaris allow a better prognosis with lower mortality rates.

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Year:  2002        PMID: 12482043     DOI: 10.1046/j.1468-3083.2002.00504.x

Source DB:  PubMed          Journal:  J Eur Acad Dermatol Venereol        ISSN: 0926-9959            Impact factor:   6.166


  12 in total

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2.  Pemphigus Vulgaris: A Clinical Study of 31 Cases (2004-2014) in Morocco.

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3.  Preliminary data on Pemphigus vulgaris treatment by a proteomics-defined peptide: a case report.

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Review 4.  Autoimmune blistering diseases in females: a review.

Authors:  Cathy Y Zhao; Dédée F Murrell
Journal:  Int J Womens Dermatol       Date:  2015-02-26

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6.  Pemphigus vulgaris and infections: a retrospective study on 155 patients.

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Review 7.  Management of Pemphigus Vulgaris.

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8.  Childhood Pemphigus Vulgaris: Report of Two Cases with Emphasis on Diagnostic Approach.

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9.  Nineteen-year retrospective evaluation of pemphigus in a single dermatology centre in Istanbul, Turkey.

Authors:  Mukaddes Kavala; İlkin Zindancı; Zafer Turkoglu; Burce Can Kuru; Emin Ozlu; Mehmet Simsek
Journal:  Postepy Dermatol Alergol       Date:  2020-03-09       Impact factor: 1.837

10.  The imbalance of gut microbiota and its correlation with plasma inflammatory cytokines in pemphigus vulgaris patients.

Authors:  Shuli Huang; Jing Mao; Lin Zhou; Xia Xiong; Yongqiong Deng
Journal:  Scand J Immunol       Date:  2019-07-08       Impact factor: 3.889

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