Literature DB >> 31009674

Nonbullous pemphigoid: Insights in clinical and diagnostic findings, treatment responses, and prognosis.

Aniek Lamberts1, Joost M Meijer2, Hendri H Pas2, Gilles F H Diercks3, Barbara Horváth2, Marcel F Jonkman2.   

Abstract

BACKGROUND: Nonbullous pemphigoid is an under-recognized phenotype of the autoimmune bullous disease pemphigoid, characterized by the absence of blisters. Several disease aspects have not been studied previously.
OBJECTIVE: To describe the characteristics of nonbullous pemphigoid.
METHODS: A retrospective review study of medical records. The diagnosis of pemphigoid was based on meeting 2 of the following 3 criteria: (1) pruritus, (2) positive direct immunofluorescence microscopy, or (3) positive indirect immunofluorescence microscopy on salt-split skin.
RESULTS: The review included 69 patients. The mean delay in diagnosis was 29 months. Skin examination most often showed pruritic papules/nodules (37%) or pruritus without primary skin lesions (22%). Histopathologic findings were mainly nonspecific. Results of direct and indirect immunofluorescence microscopy were positive in 60% and 69%, respectively. During follow-up, blisters formed in 17%, which was associated with a positive indirect immunofluorescence microscopy (P = .014) and a positive BP180 immunoblot result (P = .032). The Kaplan-Meier estimates of mortality at 1, 2, and 3 years were 14%, 34%, and 46%, respectively, with an 8.6-fold increased all-cause mortality risk. LIMITATIONS: The retrospective study design.
CONCLUSIONS: Nonbullous pemphigoid presented with heterogeneous pruritic skin lesions, resulting in delayed diagnosis. Direct and indirect immunofluorescence microscopy are essential to diagnose nonbullous pemphigoid, in contrast to histopathology, mainly showing nonspecific findings. An increased all-cause mortality risk was observed during follow-up.
Copyright © 2019 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.

Entities:  

Keywords:  autoimmune blistering disease; autoimmune bullous disease; case series; clinical characteristics; mortality; nonbullous pemphigoid; pemphigoid; prognosis; treatment

Mesh:

Substances:

Year:  2019        PMID: 31009674     DOI: 10.1016/j.jaad.2019.04.029

Source DB:  PubMed          Journal:  J Am Acad Dermatol        ISSN: 0190-9622            Impact factor:   11.527


  5 in total

1.  Non-bullous Lichen Planus Pemphigoides: A Case Report.

Authors:  Aniek Lamberts; Gilles F H Diercks; Hendri H Pas; Barbara Horváth
Journal:  Acta Derm Venereol       Date:  2020-05-28       Impact factor: 3.875

2.  Autoreactive Peripheral Blood T Helper Cell Responses in Bullous Pemphigoid and Elderly Patients With Pruritic Disorders.

Authors:  Dario Didona; Luca Scarsella; Milad Fehresti; Farzan Solimani; Hazem A Juratli; Manuel Göbel; Stefan Mühlenbein; Lily Holiangu; Josquin Pieper; Vera Korff; Thomas Schmidt; Cassian Sitaru; Rüdiger Eming; Michael Hertl; Robert Pollmann
Journal:  Front Immunol       Date:  2021-03-25       Impact factor: 7.561

Review 3.  Dermatology for the internist: optimal diagnosis and management of atopic dermatitis.

Authors:  Shanthi Narla; Jonathan I Silverberg
Journal:  Ann Med       Date:  2021-12       Impact factor: 4.709

Review 4.  The significance of preclinical anti-BP180 autoantibodies.

Authors:  Yosuke Mai; Kentaro Izumi; Shoko Mai; Hideyuki Ujiie
Journal:  Front Immunol       Date:  2022-08-08       Impact factor: 8.786

5.  IgE autoantibodies in serum and skin of non-bullous and bullous pemphigoid patients.

Authors:  A Lamberts; N Kotnik; G F H Diercks; J M Meijer; G Di Zenzo; H H Pas; M F Jonkman; B F Gibbs; U Raap; B Horváth
Journal:  J Eur Acad Dermatol Venereol       Date:  2020-11-17       Impact factor: 6.166

  5 in total

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