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Un caso de síndrome asintomático de Cronkhite-Canadá diagnosticado por hallazgos endoscópicos y patológicos
Yusaku Yokotani1,2, Hiroaki Kitae1, Mika Mazaki1
1Department of Gastroenterology, Omihachiman Community Medical Center, Omihachiman, JPN.
Este estudio de caso analiza el síndrome de Cronkhite-Canadá (SCC), una enfermedad rara. La intervención temprana con corticosteroides puede prevenir el desarrollo de síntomas en pacientes con posible SCC, incluso sin los síntomas típicos.
Área de la Ciencia:
- Gastroenterología
- Enfermedades raras
Sus antecedentes:
- El síndrome de Cronkhite-Canadá (SCC) es un trastorno raro y no hereditario.
- El diagnóstico implica síntomas característicos, anomalías ectodérmicas y hallazgos endoscópicos / patológicos específicos.
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