Dear Editor,Hailey-Hailey disease, also called benign familial pemphigus, is an autosomal dominant
disorder caused by mutations in the ATP2C1 gene. Positive family history is detected in
two thirds of all cases. The prevalence is 1:50,000 and the incidence of sporadic
mutations might be as high as 26%.[1,2] We present a case of a patient who
developed benign familial pemphigus in the seventh decade of life without any medical
family history.A 78-year-old white woman with hypertension and dyslipidemia presented with erythematous
plaques in the groin with satellite pustules diagnosed as candidal intertrigo. The
lesions had presented for 4 months and showed no improvement under topical and oral
antifungal treatment (Figure 1). The patient
reported severe itching. In two weeks' time, a new perineal erythema appeared with
linear erosions and eczematous, circinate lesions with some flaccid vesicles involving
her neck, back, and upper and lower extremities (Figure
2). The mucosal membranes were not involved. Blood test results were normal
and cultures were negative. A punch biopsy of the perineal lesions was obtained and
stained with hematoxylin-eosin and another punch was taken and studied through direct
immunofluorescence. Indirect immunofluorescence was negative. Pathology data revealed
hyperkeratosis and acanthosis with suprabasal acantholysis, which did not affect adnexal
structures and resembled a "dilapidated brick wall" (Figure 3). Dyskeratotic keratinocytes were not observed. Direct
immunofluorescence study showed no deposition of immunoreactants. These features were
consistent with Hailey-Hailey's disease.
Figure 1
Erythematous plaques with linear erosions
Figure 2
Erythematous plaques and circinate lesions on the lower extremities
Figure 3
Acanthosis with suprabasal acantholysis. Dyskeratotic keratinocytes are not
observed. Hematoxylin and eosin stain
Erythematous plaques with linear erosionsErythematous plaques and circinate lesions on the lower extremitiesAcanthosis with suprabasal acantholysis. Dyskeratotic keratinocytes are not
observed. Hematoxylin and eosin stainSymptoms include erythematous plaques with blisters and fissures that appear
predominantly in skin folds, sometimes with a circinate pattern. Many triggers have been
identified (friction, perspiration, ultraviolet radiation). Most patients have worse
symptoms during hot summer months when sweat and friction aggravate the eruption. Since
the condition usually appears in the third or fourth decade, the onset of clinical
manifestations in the seventh decade is uncommon. Lesion infection is the main problem
because it causes pain, itching, and an unpleasant smell, with the associated adversity.
White bands on the fingernails and pits on the palms can also occur. Dissemination or
mucosal involvement is rare.The diagnosis of Hailey-Hailey disease requires differentiation from other acantholytic
dermatoses. Due to the localization of the lesions, differential diagnosis also includes
candidal intertrigo, psoriasis inversa, and contact dermatitis. Although herpes simplex
infection can mimic the vesicular lesions of Hailey-Hailey disease, Tzanck smear is
useful to differentiate the diseases.[3]There is no first-line treatment. However, wearing light and loose clothes to prevent
sweating and friction is an important precaution. The most extended treatment includes
topical and systemic antibiotics, topical and systemic corticosteroids, steroidsparing
immunomodulators, botulinum toxin injections, retinoids, and dapsone. Although medical
treatment is important in the control of disease exacerbations in Hailey-Hailey, many
cases are recalcitrant, and medical therapy infrequently leads to prolonged
remissions.Carbon dioxide laser ablation is an option for recalcitrant Hailey-Hailey.[4] If the disease causes extreme
disability, surgery can be performed, with the use of grafts and flaps. Oxybutynin is an
anti-muscarinic drug that was first associated with the resolution of hyperhidrosis in
1988. In our case, the patient made outstanding progress thanks to the administration of
5 mg/daily of this antiperspirant agent since sweat is one of the precipitating factors
of new outbreaks.[5]
Authors: Phillip C Hochwalt; Kevin N Christensen; Sean R Cantwell; Thomas L Hocker; Clark C Otley; Jerry D Brewer; Christopher J Arpey; Randall K Roenigk; Christian L Baum Journal: Int J Dermatol Date: 2015-09-04 Impact factor: 2.736