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CLINICAL REPORT
Topical Steroid Withdrawal: A Case Series of 10 Children
Belinda SHEARY
Royal Randwick Medical Centre, Randwick, Australia
Concerns about topical steroid withdrawal are causing
some patients to cease long-term topical corticoste-
roid therapy, however, little is known about the en-
suing clinical outcomes. This qualitative case series
studied 10 children whose parents stopped their chro-
nic topical corticosteroid use and subsequently develo-
ped features typically reported in adults experiencing
topical steroid withdrawal. Patients were seen in an
Australian general practice between April 2014 and
October 2018, with follow-up periods ranging from 18
months to 4 years. Symptoms were difficult initially
for the children and their families, however, all ultima-
tely improved. At the final review, 4 of the children
had clear skin and another 4 had symptoms consistent
with their original, pre-treatment atopic dermatitis.
More research is required into long-term topical corti-
costeroid use and its discontinuation, including topical
steroid withdrawal, particularly in the pediatric popu-
lation.
Key words: topical steroid withdrawal; red skin syndrome;
atopic dermatitis; topical corticosteroids; eczema.
Accepted Feb 7, 2019; E-published Feb 8, 2019
Acta Derm Venereol 2019; 99: 551–556.
Corr: Belinda Sheary, Royal Randwick Medical Centre, 70/73-115 Bel-
more Road, Randwick NSW 2031, Australia. E-mail: belinda.sheary@ipn.
com.au
C
oncerns about topical steroid withdrawal (TSW)
are causing some parents of children with chronic
dermatological conditions, particularly atopic dermati-
tis (AD), to discontinue their child’s long-term topical
corticosteroid (TCS) therapy. TSW is a potential adverse
effect of TCS overuse (1), most commonly seen in pa-
tients with a history of atopy, reporting prolonged TCS
overuse, especially where such use has included the face
and provided diminishing clinical benefit over time. TSW
is widely discussed in social media (1) and with many
patients (and parents) researching health issues online
(2), discussing TSW is likely to become an increasingly
common scenario for prescribers of TCSs (3).
Pediatric cases of TSW have been reported in the
literature infrequently (1, 4–6). The incidence and preva-
lence of TSW is unknown (1, 7) and research is limited
(6, 8–13), however, a systematic review (1) suggested
TSW in children is uncommon with only 7% of reported
cases occurring in patients under 18 years of age. In a
recent study (12) examining patients ceasing long-term
TCSs and subsequently developing TSW symptoms,
20% (14 out of 69) of patients were children. This paper
SIGNIFICANCE
Topical steroid withdrawal is discussed widely in social me-
dia, and some patients with a history of long-term topi-
cal steroid use are self-diagnosing this condition. There is
little information in medical literature about what happens
when chronic topical steroid therapy is stopped, especially
in children. This study followed 10 children for between 18
months and 4 years after their parents decided to cease
their topical steroid use. The children experienced typical
topical steroid withdrawal symptoms for many months,
however, all eventually improved.
examines the histories of 10 of those 14 children. They
were followed up in a general practice setting for 18
months–4 years.
Little is known about what happens when children
cease chronic TCS use. Patients may experience “re-
bound” symptoms after stopping TCSs (14) and certainly
after stopping oral steroids for skin symptoms (15). Ho-
wever, it is not widely accepted there may be withdrawal
symptoms associated with TCS discontinuation as it is
with other medication (for example, selective serotonin
reuptake inhibitors commonly prescribed for depres-
sion). This may be because traditionally TCSs have been
recommended intermittently for flares of symptoms and
long-term frequent use has not been studied. However,
in practice there are patients who use TCSs regularly
for years – sometimes on a continuous daily basis (12).
Confirming the diagnosis of TSW is problematic,
and TSW remains controversial. Accepted diagnostic
criteria for TSW do not exist (though recently some
have been proposed (12)), and TCS “overuse” has never
been defined. Some argue that the symptoms resulting
from TCS discontinuation represent an exacerbation of
the underlying skin disease, however, there are features
typically reported in TSW and not in AD. On ceasing
TCSs, a patient with TSW develops widespread red skin
(7, 10–11) and itch, in addition to at least some of the
following distinctive features: burning pain, excessive
skin exfoliation, edema, skin sensitivity (1, 7, 10, 12),
‘red sleeve’ (7, 12) and/or ‘elephant wrinkles’ (12).
MATERIAL AND METHODS
This case series examined the histories of patients under the age of
18, who presented to an Australian general practice with concerns
about TSW, and whose cases were reported to the Therapeutic
Goods Administration (for inclusion in the Australian Adverse
Drug Reaction Database) between January 2015 and February
This is an open access article under the CC BY-NC license. www.medicaljournals.se/acta
Journal Compilation © 2019 Acta Dermato-Venereologica.
doi: 10.2340/00015555-3144
Acta Derm Venereol 2019; 99: 551–556