A case report of Peutz-Jeghers syndrome in a child with Crohn's disease.

JPGN reports Pub Date : 2026-04-09 eCollection Date: 2026-08-01 DOI:10.1002/jpr3.70184
Hasala Rannulu, Eve May, Bethany Cunningham, Eric Cochran, Rachel Zdenek, Stefany H Garrity
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Abstract

Peutz-Jeghers syndrome (PJS) is a rare genetic disorder characterized by hamartomatous polyps and mucocutaneous hyperpigmented freckles, whereas Crohn's disease (CD) is a condition characterized by chronic intestinal inflammation. Here, we present a rare case report of an 11-year-old male who presented with both CD and PJS. To our knowledge, this is only the fifth case report describing both of these diseases in the same patient. While CD is relatively common in industrialized countries, having CD in conjunction with PJS is exceedingly rare. This paucity of data describing the coexistence of the two conditions in the same patient has led to a general lack of guidance and screening recommendations in patients with both of these diseases. It is known that each disorder alone increases a patient's risk of malignancy; however, more data are needed to determine the appropriate cancer screening algorithm for patients with these dual diagnoses as well as management approaches.

克罗恩病儿童Peutz-Jeghers综合征1例报告。
Peutz-Jeghers综合征(PJS)是一种罕见的遗传性疾病,其特征是错构瘤息肉和粘膜皮肤色素沉着雀斑,而克罗恩病(CD)是一种以慢性肠道炎症为特征的疾病。在这里,我们提出一个罕见的病例报告,一个11岁的男性谁提出了CD和PJS。据我们所知,这是在同一患者中描述这两种疾病的第五例报告。虽然乳糜泻在工业化国家相对常见,但乳糜泻与PJS合并是极其罕见的。由于缺乏描述同一患者中这两种情况共存的数据,导致对患有这两种疾病的患者普遍缺乏指导和筛查建议。众所周知,每一种疾病本身都会增加患者患恶性肿瘤的风险;然而,需要更多的数据来确定适合这些双重诊断患者的癌症筛查算法以及管理方法。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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