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1.
An. bras. dermatol ; 93(4): 585-586, July-Aug. 2018. graf
Article in English | LILACS | ID: biblio-949923

ABSTRACT

Abstract: Harlequin syndrome is a rare condition in which one half of the face fails to flush and sweat due to damage of the sympathetic fibers on the ipsilateral side. The majority of cases are idiopathic, but may be iatrogenic or caused by space-occupying lesions or brainstem infarction. We report a case of idiopathic harlequin syndrome in a 34-year-old man with a 5-month history of unilateral facial flushing and sweating after exercise. Despite the rarity of this syndrome, dermatologists should be aware of this condition in order to diagnose properly and provide multidisciplinary assistance.


Subject(s)
Humans , Male , Adult , Autonomic Nervous System Diseases/diagnosis , Flushing/diagnosis , Hypohidrosis/diagnosis
2.
An. bras. dermatol ; 92(5,supl.1): 37-39, 2017. graf
Article in English | LILACS | ID: biblio-887065

ABSTRACT

Abstract: Bullous systemic lupus erythematosus (BSLE) is a rare autoimmune subepidermal blistering disease, with few cases described in childhood. It has different clinical-pathological features. We report a case of BSLE in a 10-year-old child with systemic lupus erythematosus, treated with prednisone and hydroxychloroquine. There was complete remission with dapsone, with no recurrence of skin lesions throughout one year of follow-up. We highlight the rarity and early age of occurrence.


Subject(s)
Humans , Female , Child , Blister/pathology , Lupus Erythematosus, Systemic/pathology , Basement Membrane/pathology , Biopsy , Blister/drug therapy , Fluorescent Antibody Technique, Direct , Rare Diseases/pathology , Rare Diseases/diagnostic imaging , Lupus Erythematosus, Systemic/drug therapy
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