Multiple Choice: ERYTHEMATOVIOLACEOUS MACLES ON TONGUE

Authors

  • María Belén Godoy Hospital de Clínicas Pte. Dr. Nicolás Avellaneda, San Miguel de Tucumán, Tucumán, Argentina

DOI:

https://doi.org/10.47196/da.v29i3.2491

Keywords:

macles, tongue

Abstract

A 59-year-old woman, originally from San Miguel de Tucumán, with a history of multiple hospitalizations since 2019 for anemic syndrome and heart failure, without a definitive diagnosis. She was admitted to the guard in poor general condition, asthenic, adynamic, with generalized cutaneous-mucous pallor, edema of the lower limbs, upper gastrointestinal bleeding and epistaxis. In the facial region she presented multiple brownish papules with a rough surface, rounded, with well-defined edges (Photo 1). On the dorsum of the tongue, short fissures distributed evenly, and multiple macules and erythematopurpuric papules of years of evolution (Photo 2). During her hospitalization in the Medical Clinic room, a Dieulafoy lesion with active bleeding was evident in upper digestive video endoscopy. Polypoid lesions at the level of the sigmoid and cecum in colonoscopy. She presented non-reactive serologies and tumor markers within normal values. In the abdominal tomography: diffusely enlarged liver with a non-homogeneous structure, marked increase in the diameter of the inferior vena cava and suprahepatic veins, so a hepatosplenic Doppler ultrasound was requested where multiple enlarged, tortuous intrahepatic arterial routes were recognized. and with high flow rate.

Author Biography

María Belén Godoy, Hospital de Clínicas Pte. Dr. Nicolás Avellaneda, San Miguel de Tucumán, Tucumán, Argentina

Dermatology Resident

References

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II. Del Azar NE, Rossi MV, García S, Tessadro G, et ál. Telangiectasia hemorrágica hereditaria. Dermatol Argent. 2017;23:38-41.

III. Orizaga-Quiroga TL, Villarreal-Martínez A, Jaramillo-Moreno G, Ocampo-Candiani J. Síndrome de Osler-Weber-Rendu y su relación con la dermatología. Actas Dermo-Sifiliográficas. 2019;110:526-532.

IV. Serra MM. Telangiectasia hemorrágica hereditaria (síndrome de Rendu-Osler-Weber) Rev Hosp Ital B. Aires 2014;34:41-50.

Published

2023-12-01

Issue

Section

Young Dermatologists