Griffi et al, 2010; Voorhees et al, 2019; Saikaly et al,
2016; Hoegler et al, 2018).
The pathogenesis of GPP is only partially
understood. GPP can present in patients with
existing or prior psoriasis Vulgaris or in patients
without a history of psoriasis Vulgaris. More than
half of the GPP individual cases are caused by
recessive mutations in IL36RN. IL36RN encodes
interleukin-36-receptor antagonist (IL-36Ra), which
antagonizes three interleukin cytokines (IL-1F6, IL-
1F8, and IL-1F9) that are involved in the activation
of pro-inflammatory signaling pathways (Hoegler et
al, 2018).
The clinical presentation of generalized pustular
psoriasis usually presents with 2-3 mm sterile
pustules overlying painful, erythematous skin.
Patients are visibly ill, with high-grade fever,
malaise, leucocytosis, elevated C-reactive protein
levels (Hoegler et al, 2018). Diagnostic criteria
proposedby Umezama et al. are consisted of 1)
multiple sterile pustules overlying erythematous
skin, 2) fever, malaise and other systemic symptoms,
3) Kogoj spongiform pustules on histopathological
analysis, 4) laboratory abnormalities including left
shift leucocytosis, elevated erythrocyte
sedimentation rate, elevated CRP, elevated ASTO
levels, elevated IgG or IgA levels, hypoproteinemia,
hypocalcaemia, 5) recurrence of these
clinical/histopathological features. (Hoegler et al,
2018) The differential diagnosis of pustular psoriasis
is with acute generalized exanthematous pustulosis
(AGEP), but AGEP tends to occur and resolve more
quickly and is particularly associated with antibiotic
use (Hoegler et al, 2018).
For the diagnostic examination, we can do a
biopsy for a histopathology examination. The
histopathology findings in pustular psoriasis consist
of confluent parakeratosis, hyperkeratosis,
neutrophils in stratum corneum (Munro
microabscesses) and in spinous layer (spongiform
pustules of Kogoj), hypergranulosis,sub-
parapapillary thinning of the epidermis, regular
acanthosis, often with clubbed rete ridges, dilated
capillaries in dermal papillae, perivascular
lymphocytes (Rapini, 2012).
A broad spectrum of antipsoriatic treatments,
both topical and systemic, is available for the
management of psoriasis (Gudjonsson et al, 2012).
In patients with erythrodermic and pustular
psoriasis, treatments with acitretin, methotrexate, or
short-course cyclosporine are the treatments of the
first choice (Gudjonsson et al, 2012).
For children
with GPP, first-line treatment is similar to that
inadults.As retinoids can cause premature epiphyseal
closure,skeletal hyperostosis, and extraosseous
calcification, it maynot be ideal first-line therapy.
Cyclosporine has fewer knownsideeffects and is
often the first treatment used before
retinoids.Methotrexate is not approved in children
under the age of 2 years.Both methotrexate and
cyclosporine must be used with cautionbecause of
the long-term oncogenic potential.A recent
retrospective chart review assessed the efficacy of
cyclosporine in pediatric patients having extensive
plaquetype, erythrodermic, and pustular psoriasis.
Excellent efficacy (>75% reduction in PASI) was
observed in all but three patients (Gudjonsson et al,
2012; Rapini, 2012; Dogra et al, 2017; James et al,
2016; Dogra et al, 2018). Corticosteroids shouldbe
utilized with caution, especially in patients with
concomitantpsoriasis Vulgaris because of the
potential to initiate flares.Combination therapies are
employed in almost 50% of the children with
generalized pustular psoriasis in order to provide
optimum disease control. Pustular psoriasis in
children has a more favorable course as compared to
adults. The response to treatment is good, and
remission lasts longer as compared to adults (Dogra
et al, 2018).
2 CASE
A nine-year-oldboy, Indonesian people, Javanese,
was brought by her parents to the dermato-
venereology clinic in Karyadi General Hospital on
August 10
th
, 2018 with a chief complaint ofsudden
onset of pustules eruptions on an erythematous
baseover the face, trunk, and extremities.
The lesions were developed within 24 h after the
patient got vaccinated in his school. The lesion was
initially on his face then became more generalized
with the involvement of the face, trunk, and
extremities. The symptoms were alsoaccompanied
by fever and pain on his body.Then his parents
brought him to a dermatologist. There he received
treatment with topical cream and oral capsule, but
the lessons did not improve, so he was referred to
Karyadi Hospital.
The patient did not suffer from any other
diseases or use any topical or systemic medication
before. He had no food or drug allergy. Therewas no
past and family history of dermatosis, including
psoriasis. The patient was the first child, and he has
a healthy 5-year-old little brother. He was in 2
nd
-
grade junior high school, and his academic status
was functional. His parents worked as an employee.