Zovko Zeljko, Boscarelli Alessandro, Codrich Daniela, Bussani Rossana, Neri Francesca, Schleef Jürgen
Department of Pediatric Surgery and Urology, Institute for Maternal and Child Health-Istituto di Ricovero e Cura a Carattere Scientifico "Burlo Garofolo", via dell'Istria, 65/1, 34137 Trieste, Italy.
Department of Surgery, University Hospital of Mostar, 88000 Mostar, Bosnia and Herzegovina.
Children (Basel). 2025 Apr 3;12(4):461. doi: 10.3390/children12040461.
Lipomas are among the most encountered neoplasms in clinical practice, occurring mainly in adults between the fourth and sixth decades of life. Deep-seated lipomas in children are found in the thorax, chest wall, mediastinum, pleura, pelvis, retroperitoneum, and paratesticular area. Herein, we present a case of a three-year-old child with a giant mesenteric lipoma, along with a review of the literature on mesenteric lipomas in childhood.
A three-year-old male toddler was referred to our hospital for severe, intermittent abdominal pain. Imaging studies at admission revealed a fat lesion occupying most of the peritoneal cavity and dislocating adjacent structures. An urgent laparotomy was performed. A giant lipoma arising from the mesentery and leading to the torsion of the mesenteric radix was confirmed and completely excised alongside an adherent small tract of jejunum. The child recovered uneventfully and is still being followed-up with no signs of recurrence.
Lipomas of the mesentery in children are very rare, and they are reported to be more common among children younger than three years of age. Mesenteric lipomas appeared to be more frequent in males than females. Even though they might be asymptomatic, voluminous lipomas can also create a lead point for intermittent torsion of the mass causing ischemia and infarction. Abdominal pain was the most frequent symptom, and the ileum was the tract of bowel more frequently involved by the tumor. Laparotomy was reported to be the preferable approach to safely remove this abdominal mass, especially in case of huge dimensions.
脂肪瘤是临床实践中最常遇到的肿瘤之一,主要发生于40至60岁的成年人。儿童深部脂肪瘤见于胸部、胸壁、纵隔、胸膜、骨盆、腹膜后和睾丸旁区域。在此,我们报告一例3岁儿童巨大肠系膜脂肪瘤病例,并对儿童肠系膜脂肪瘤的相关文献进行综述。
一名3岁男童因严重间歇性腹痛转诊至我院。入院时的影像学检查显示一个脂肪性病变占据了大部分腹腔并使相邻结构移位。遂行急诊剖腹手术。证实为一个起源于肠系膜并导致肠系膜根部扭转的巨大脂肪瘤,连同一小段粘连的空肠一并完整切除。患儿恢复顺利,目前仍在随访中,无复发迹象。
儿童肠系膜脂肪瘤非常罕见,据报道在3岁以下儿童中更为常见。肠系膜脂肪瘤在男性中似乎比女性更常见。尽管它们可能无症状,但巨大的脂肪瘤也可能成为肿物间歇性扭转的起始点,导致缺血和梗死。腹痛是最常见的症状,肿瘤最常累及的肠段是回肠。据报道,剖腹手术是安全切除这种腹部肿物的首选方法,尤其是在肿物巨大的情况下。