Bannayan Zonana Syndrome: An Unusual Cause of Intussusception and Protein Losing Enteropathy in a Child

Maaloul Ines, B. Mahdi, Cheikhrouhou Taycir, Z. Mohamed, Aloulou Hajer, M. Riadh, Benazzou Salma, Kamoun Thouraya
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Abstract

Bannayan-Zonana syndrome (BRRS) is a rare genetic disorder characterized by macrocephaly, numerous soft tissue and visceral hamartomas, and lipomas. Because of the risk of fatal bleeding and visceral neoplasia in adulthood, recognizing this disease is critical. We reported a new pediatric case of BRRS in an 18-month-old female infant with lipomas, macrocephaly, and gastrointestinal hamartomatous polyps that prompted ileo-ileal intussusception and protein-losing enteropathy. Patients with BRRS require a comprehensive approach. Our case is unique in its sporadic occurrence and the presence of protein-losing enteropathy as a gastrointestinal polyposis manifestation. Pediatric patients with multiple lipomas, protein-losing enteropathy, and intestinal intussusception should be assessed for BRRS.
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Bannayan Zonana综合征:儿童肠套叠和蛋白质丢失肠病的罕见原因
Bannayan-Zonana综合征(BRRS)是一种罕见的遗传性疾病,其特征是小头畸形、大量软组织和内脏错构瘤以及脂肪瘤。由于成年后有致命出血和内脏肿瘤的风险,认识到这种疾病至关重要。我们报告了一例新的儿科BRRS病例,该病例发生在一名18个月大的女婴身上,她患有脂肪瘤、小头畸形和胃肠错构瘤性息肉,导致回肠肠套叠和蛋白质丢失肠病。BRRS患者需要综合治疗。我们的病例是独特的,其散发性发生和蛋白质丢失肠病作为胃肠道息肉病的表现。患有多发性脂肪瘤、蛋白质丢失肠病和肠套叠的儿童患者应进行BRRS评估。
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