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

J Am Acad Dermatol. 2019 Aug;81(2):355-363. doi: 10.1016/j.jaad.2019.04.029. Epub 2019 Apr 19.

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.

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

MeSH terms

  • Adult
  • Aged
  • Aged, 80 and over
  • Autoantibodies / blood*
  • Autoantigens / immunology*
  • Autoimmune Diseases / diagnosis*
  • Autoimmune Diseases / immunology
  • Autoimmune Diseases / pathology
  • Collagen Type XVII
  • Delayed Diagnosis
  • Dystonin / immunology*
  • Female
  • Fluorescent Antibody Technique, Direct
  • Fluorescent Antibody Technique, Indirect
  • Humans
  • Kaplan-Meier Estimate
  • Male
  • Microscopy, Fluorescence
  • Middle Aged
  • Non-Fibrillar Collagens / immunology*
  • Prognosis
  • Pruritus / etiology
  • Retrospective Studies
  • Skin Diseases / diagnosis*
  • Skin Diseases / immunology
  • Skin Diseases / pathology
  • Survival Rate

Substances

  • Autoantibodies
  • Autoantigens
  • DST protein, human
  • Dystonin
  • Non-Fibrillar Collagens