Case of Erythema Annulare Centrifugum

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Annually recurring erythema annulare centrifugum: a case report

INTRODUCTION Erythema annulare centrifugum is a rare cutaneous disease characterized by erythematous and violaceous annular plaques that usually involved the thighs and the legs. The eruption may be associated with an underlying disease and its accompanying characteristic symptoms. For these reasons, a full physical examination should be conducted to exclude underlying disorders. Annually recur...

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Erythema Annulare Centrifugum: A Rare Skin Finding of Autoimmune Hepatitis

Erythema annulare centrifugum is characterized by dermal perivascular lymphocytic infiltrates. It is often associated with infections, autoimmune or neoplastic diseases but in most cases the cause is unexplained. A case of erythema annulare centrifugum related to autoimmune hepatitis in a 24-year-old woman is described in this case report. Clinical response of the autoimmune hepatitis to a comb...

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Erythema annulare centrifugum during rituximab treatment for autoimmune haemolytic anaemia.

References 1 Parsi K, Kossard S. Multiple hereditary glomangiomas: successful treatment with sclerotherapy. Australas J Dermatol 2002; 43: 43–47. 2 Goldman MP, Sadick NS, Weiss RA. Cutaneous necrosis, telangiectatic matting, and hyperpigmentation following sclerotherapy. Etiology, prevention, and treatment. Dermatol Surg 1995; 21: 19–29. 3 H elou J, Maatouk I, Moutran R, Wehb e J, Stephan F, Ob...

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Erythema annulare centrifugum: association with autoimmune polyglandular syndrome type 1

Autoimmune polyendocrine syndromes are a heterogeneousgroup of rare diseases characterized by autoimmune activityagainst more than one endocrine organ, although non-endocrineorgans can also be affected. We report the association of APS Iwith erythema annulare centrifugum in an 18-years-old male whopresented with multiple figurate erythema spreading on his trunkand extremities along with a histo...

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ژورنال

عنوان ژورنال: Proceedings of the Royal Society of Medicine

سال: 1939

ISSN: 0035-9157

DOI: 10.1177/003591573903200605