Bullous Pemphigoid and Scabies: Is There an Association?

September 2022 | Volume 21 | Issue 9 | 1009 | Copyright © September 2022


Published online September 1, 2022

doi:10.36849/JDD.4900

Mati Rozenblat MDa, Awad Halaj MDa, Assi Levi MDb,c, Moshe Lapidoth MDb,c, Michael Ziv MDa

aDepartment of Dermatology, "Emek" medical center, Afula, Israel
bSackler Faculty of Medicine, Tel Aviv University, Tel Aviv
cLaser Unit, Division of Dermatology, Rabin Medical Center, Petah-Tikva, Israel

Abstract
Background: Bullous Pemphigoid (BP) is an autoimmune subepithelial bullous disease. Several reports suggested an association between BP and scabies.
Objective: We aimed to evaluate whether an association between BP and scabies exists.
Methods: This is a retrospective matched case-control study. We retrospectively identified BP patients treated in our clinic between January 1, 2009, and December 31, 2016. Each patient was assigned to 3 control subjects (matched by age and sex) treated in our clinic, not due to BP. The study group was examined for a scabies diagnosis within the 3 years prior to BP diagnosis; the control group was examined for a scabies diagnosis 3 years prior to its first visit in our clinic.
Results: Fifteen out of the 87 (17.2%) BP patients were diagnosed with scabies within the 3 years prior to their initial BP diagnosis, compared to only 4.2% (11 out of 261) among the control group. The odds ratio of scabies history was 4 times higher among BP patients compared to the control group (OR=4.23; 95% CI: 1.50–11.91, P=0.007).
Limitations: A retrospective study design.
Conclusions: An association between scabies diagnosis and BP is demonstrated in our study.

J Drugs Dermatol. 2022;21(9):1009-1011. doi:10.36849/JDD.4900

INTRODUCTION

Bullous pemphigoid (BP) is one of the most common autoimmune bullous diseases. It typically affects the elderly.1 It is characterized by autoantibodies against the basement membrane zone proteins- BP antigen 1 and BP antigen 2. The disease has variable presentation; the typical one consists of tense bulla on reddish base skin and is associated with pruritus. The diagnosis is based on a characteristic clinical manifestations along with immunohistological and immunological findings. It had been found that the disease is more prevalent among certain HLA class II alleles.2 BP had been described in association with neurological diseases.3,4 In addition, several reports described an association of BP and scabies.5,6 Scabies has several clinical presentations - the classical one consists of burrows, nodules, and crusts. However, the epidemiological and clinical presentation of scabies might resemble BP, thus confusion can occur, as reported in case reports of patients with a clinical picture of BP and evidence of scabies. The possible explanations for the overlap vary from superinfection with Staph Aureus (S. Aerus), id reaction, and secretion of lytic enzymes; However, the relationship between these factors and BP is not well determined.7,8 Another possible explanation lies within the speculated pathomechanism for cases of BP induced by scabies, which suggests that exposure of autoantigens induced by a distribution of the basement membrane at the junction of the epidermis and dermis and may start a cascade that contributes to the development of BP. The process was named epitope spreading phenomenon.9 This study aims to evaluate whether an association between BP and scabies truly exists.

MATERIALS AND METHODS

Emek medical center is a tertiary referral center for dermatological patients in northeastern part of Israel. It covers a population of approximately 1 million people.10 It is the only center with an immune pathology service in the area. This population combines 2 major ethnic groups, Jews and Arabs. About 7 percent of the district population is above 65 years old according to the 2008 census.10 We searched the databases of our local health system for patients with a new diagnosis of BP which are residents of the northeastern district of Israel. The database was searched for a time period between January 1, 2009, to December 31, 2016. For each patient, we randomly assigned 3 control subjects without BP that visited our clinic for reasons other than BP. The