Anhidrosis segmentaria asociada a pupila de Adie: un caso de síndrome de Ross incompleto / Segmental anhidrosis associated with Adie’s pupil: an incomplete case of Ross syndrome

Se presenta un caso de una mujer de 43 años que presentaba una zona de anhidrosis localizada en la parte superior izquierda del tronco y extremidad superior ipsolateral. Se asociaba a una pupila tónica de Adie y a una zona de hiperhidrosis compensatoria en el lado contralateral. Tras 9 años de seguimiento, las alteraciones han permanecido estables. Estas alteraciones del sistema nervioso autónomo corresponden a un síndrome de Ross con expresión incompleta

We present the case of a 43-year-old woman who presented with a localized area of anhidrosis on the upper left trunk and ipsilateral upper limb. It was associated with Adie's tonic pupil and an area of compensatory hyperhidrosis on the contralateral side. After 9 years of follow up, the alterations have remained stable. These alterations of the autonomous nervous system correspond to an incompletely expressed Ross syndrome

[Segmental anhidrosis associated with Adie's pupil: an incomplete case of Ross syndrome]. / Anhidrosis segmentaria asociada a pupila de Adie: un caso de síndrome de Ross incompleto.

We present the case of a 43-year-old woman who presented with a localized area of anhidrosis on the upper left trunk and ipsilateral upper limb. It was associated with Adie's tonic pupil and an area of compensatory hyperhidrosis on the contralateral side. After 9 years of follow up, the alterations have remained stable. These alterations of the autonomous nervous system correspond to an incompletely expressed Ross syndrome.

Leukocytoclastic vasculitis presenting as an erythema gyratum repens--like eruption on a patient with systemic lupus erythematosus.

Cutaneous leukocytoclastic vasculitis is a common finding among patients with systemic lupus erythematosus, although the clinical appearance of the lesions varies. We report the case of a 38-year-old woman with systemic lupus erythematosus who had leukocytoclastic vasculitis with peculiar clinical morphologic features of the cutaneous lesions. They consisted of figured erythema closely resembling erythema gyratum repens. We discuss the differential diagnosis with other annular eruptions.