Literature DB >> 21727692

Bullous pemphigoid.

Sujay Khandpur1, Parul Verma.   

Abstract

Bullous pemphigoid (BP) is a relatively common autoimmune vesicobullous disease encountered in India. It is a subepidermal bullous disorder most commonly seen in the elderly and manifests as tense blisters on urticarial base, predominantly over flexures, and is associated with pruritus. The diagnosis can be confirmed by histology, direct and indirect immunofluorescence. Several new diagnostic techniques have also been developed. Treatment of BP is based on the extent and rate of progression of the disease. Several topical and systemic anti-inflammatory and immunosuppressive agents have been used with variable results.

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Year:  2011        PMID: 21727692     DOI: 10.4103/0378-6323.82398

Source DB:  PubMed          Journal:  Indian J Dermatol Venereol Leprol        ISSN: 0378-6323            Impact factor:   2.545


  3 in total

1.  Dyshidrosiform pemphigoid with Parkinsonism in a nonagenarian Maharashtrian female.

Authors:  Tabassum Behlim; Yugal K Sharma; Nitin D Chaudhari; Kedarnath Dash
Journal:  Indian Dermatol Online J       Date:  2014-10

2.  A case series of ocular involvement in bullous pemphigoid: clinical features, management, and outcomes.

Authors:  Anahita Kate; Swapna Shanbhag; Pragnya Rao Donthineni; Sayan Basu
Journal:  F1000Res       Date:  2021-11-25

3.  A Cross-sectional Study of Direct Immunofluorescence in the Diagnosis of Immunobullous Dermatoses.

Authors:  Archana C Buch; Harsh Kumar; Nk Panicker; Sonali Misal; Yk Sharma; Charusheela R Gore
Journal:  Indian J Dermatol       Date:  2014-07       Impact factor: 1.494

  3 in total

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