ARTICLE
Auteur(s) : Ricardo Coelho1,
Rodrigo Carvalho2, Ana Rodrigues2, Ana
Afonso3, Jorge Cardoso2
1Dermatology Department, Hospital de Faro
2Dermatology Department, Hospital de Curry
Cabral
3Pathology Department, Hospital de Curry Cabral
A 74-year-old white woman was referred to our department with a
1-year history of four large asymptomatic lesions on her thighs.
The lesions began as small erythematous patches and subsequently
increased in diameter. She had a history of arthritis, treated for
the preceding 3 years with naproxen.
Examination of the posterior thighs revealed four large (between
3 × 2 cm and 17 × 14 cm) erythematous, minimally scaly,
oval patches, with no induration. One of the lesions had light
central clearing (figure
1). Physical examination was otherwise unremarkable. The
initial clinical impression was parapsoriasis, and a biopsy
specimen was obtained. Histopathological examination revealed a
moderate superficial and mid-dermal interstitial infiltrate of
lymphocytes and histiocytes, and mucin between collagen fibers;
these findings are consistent with the interstitial variant of
granuloma annulare. Further investigations were unremarkable. The
diagnosis of patch-type granuloma annulare was made, and the
patient was treated with betamethasone ointment twice daily for 4
weeks with no improvement. We did not find any regression of the
lesion after biopsy. Because the lesions were asymptomatic and
caused no anxiety to the patient, topical medication was
discontinued.
Granuloma annulare is a benign, self-limited condition; the
cause is unknown and the pathogenesis is poorly understood. There
are several clinical variants of granuloma annulare: localized,
generalized, subcutaneous, perforating, linear, and patch types.
There is an overlap between variants, and more than one
morphological type may exist in the same patient. This patient had
a rare, recently described granuloma annular variant named patch
granuloma annulare [1]. It appears as asymptomatic erythematous to
brown patches, with or without minimal scale, that may have an
annular configuration on the trunk or proximal extremities. There
is no evidence of papules, scales, or induration [2]. As with other
forms of granuloma annulare, there is a female predominance. There
is also a possible association with drug reaction (which may have
been present in our patient) [1-3].
A high index of suspicion is necessary to make the diagnosis.
The differential diagnosis of patch-type granuloma annulare
includes morphea, erythema annulare centrifugum, and parapsoriasis.
Pathologically, this entity is characterized by an interstitial
pattern of mononuclear cellular infiltration with scattered
histiocytes between collagen fibers; there is mucin deposition
between collagen bundles that can be highlighted by Alcian blue and
colloidal iron stains [4]. Necrobiotic areas are usually absent. In
cases related to drug reactions, eosinophils and some lichenoid
changes at the dermal-epidermal interface are present. Histological
differential diagnosis includes necrobiosis lipoidica and
interstitial granulomatous dermatitis. Systemic therapy is
unnecessary because of the relatively limited involvement and
asymptomatic nature of the lesions. It is reported that patch
granuloma annulare will respond to the same therapy as other types
of granuloma annulare: cryotherapy, topical and intralesional
corticosteroids for localized disease, and photochemotherapy,
isotretinoin, dapsone, or antimalarials for generalized disease.
Resolution of patch-type granuloma annulare after biopsy has been
reported [5].
In conclusion, we present a rare and recently described variant
of granuloma annulare characterized by patches of erythema on the
extremities and trunk that lack the usual clinical findings but
display the classic histopathological findings of interstitial
granuloma annulare.
Acknowledgements
Financial support: none. Conflict of interest: none.
References
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