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- W4386905632 abstract "Peutz-Jeghers syndrome (PJS) is an autosomal dominant syndrome with an incidence of 1 in 200,000 live births. The most frequent clinical manifestations are hyperpigmented macules typically located on the oral mucosa and the presence of polyposis in the gastrointestinal tract. Unlike adulthood, in pediatrics the development of malignant tumor pathology is exceptional. However, in the pediatric age group, a high index of suspicion must be maintained when faced with a patient diagnosed with PJS who presents with abdominal pain compatible with intussusception, since this complication is relatively frequent and requires urgent surgical treatment. Once the diagnosis of this disease has been made, periodic controls should be carried out by means of endoscopies starting at eight years of age." @default.
- W4386905632 created "2023-09-21" @default.
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- W4386905632 date "2023-09-15" @default.
- W4386905632 modified "2023-10-05" @default.
- W4386905632 title "Máculas hiperpigmentadas y prolapso rectal, ¿qué debemos sospechar?" @default.
- W4386905632 doi "https://doi.org/10.60147/eb5053f7" @default.
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