Bier anemic spots, cyanosis, and urticaria-like eruption comprise the recently defined BASCULE syndrome. This rare and benign condition has been reported in approximately 15 individuals in the literature. We present three new cases of BASCULE syndrome occurring in adolescents with interesting associations.
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| http://dx.doi.org/10.1177/2050313X231152062 | DOI Listing |
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[Translated article] Adult-Onset BASCULE Syndrome.
Actas Dermosifiliogr
September 2024
Servicio de Anatomía Patológica, Hospital Universitari General de Catalunya, Grupo Hospitalario Quirón Salud, Sant Cugat del Vallés, Barcelona, Spain.
Reply to "BASCULE syndrome: Additional evidence for the association with autonomic dysfunction".
Pediatr Dermatol
May 2024
Department of Dermatology, Mayo Clinic, Rochester, Minnesota, USA.
BASCULE syndrome: Additional evidence for the association with autonomic dysfunction.
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March 2024
Department of Pediatric Infectious Diseases and Immunology, Arnaud de Villeneuve University Hospital of Montpellier, Montpellier, France.
Bier anemic spots, cyanosis, and urticaria-like eruption (BASCULE) syndrome in a 15-year-old male, responsive to high-dose fexofenadine.
Pediatr Dermatol
July 2024
Department of Dermatology, Tallaght University Hospital, Dublin 24, Ireland.
We describe an unusual presentation of Bier anemic spots, cyanosis, and urticaria-like eruption (BASCULE) syndrome in a 15-year-old male, recalcitrant to low-dose anti-histamines, which subsequently responded to high-dose fexofenadine.
View Article and Find Full Text PDFBridging the gap in BASCULE syndrome: A retrospective case series of a recently described clinical entity.
Pediatr Dermatol
January 2024
Department of Dermatology, Mayo Clinic, Rochester, Minnesota, USA.
Background: Bier anemic spots, cyanosis with urticaria-like eruption (BASCULE) syndrome is a recently described entity with episodic urticarial lesions and white anemic halos on a background of erythrocyanosis, commonly affecting the lower extremities. Possible association with autonomic dysfunction remains poorly understood. Existing publications are limited, but the condition is suggested as highly underrecognized.
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