意想不到的目标:佩茨-杰格综合征

Alessandro Neirotti, Francesca Parola, Sabrina Scarcia, Adalberto Maria Brach Del Prever, L. Rossi
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引用次数: 0

摘要

佩兹-杰格尔斯综合征(Peutz-Jeghers Syndrome)是一种遗传病,患者有可能患肿瘤变性和胃肠道并发症。在大多数情况下,腹痛是导致患者到急诊室就诊的急性症状。这可能是由于出血息肉和肠套叠等危险的病症引起的。肠套叠的临床表现最初可能很微妙,呈间歇性模式,但可能被低估,因为患儿可能会交替出现剧烈疼痛和完全康复的阶段。论文强调,即使肠套叠在两岁以上儿童中是一种罕见的病理现象,也必须始终将伴有呕吐的剧烈绞痛纳入肠套叠的鉴别诊断中。临床医生必须对非典型年龄的肠套叠患者进行有针对性的病史分析,以调查继发原因。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Un bersaglio quando meno te lo aspetti: la sindrome di Peutz-Jeghers
Peutz-Jeghers Syndrome is a genetic condition that puts affected patients at risk of oncological degeneration and gastrointestinal complications. In most cases, abdominal pain is the acute symptom that leads the patient to the emergency room. This may be due to dangerous medical conditions, such as bleeding polyps and intussusception. The clinical presentation of intussusception might initially be subtle with an intermittent pattern that may be underestimated as the child may alternate intense pain with phases of complete well-being. The paper underlines that intense colic pain associated with emesis must always be included in the differential diagnosis of intestinal intussusception, even if it is a rare pathology in children over 2 years of age. The clinician must conduct a targeted anamnesis to investigate secondary causes in a patient with possible intussusception at a non-typical age.
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