Miscia Maria Enrica, Lisi Gabriele, Lauriti Giuseppe, Riccio Angela, Di Renzo Dacia, Cascini Valentina, Lelli Chiesa Pierluigi
Department of Pediatric Surgery, "Spirito Santo" Hospital, Pescara, Italy.
Department of Medicine and Aging Sciences, "G. d'Annunzio" University, Chieti-Pescara, Italy.
Case Rep Surg. 2020 Jul 24;2020:3018065. doi: 10.1155/2020/3018065. eCollection 2020.
Giant mesenteric lipoblastoma is a rare benign tumor arising from the adipocytes. It can mimic malignant tumors, and its diagnosis is difficult before surgery. Imaging studies could lead the diagnosis but not confirm it. Those tumors arising in the abdomen are usually larger and can cause symptoms of compression. Surgical excision is the treatment of choice, and a long-term follow-up is necessary to detect local recurrences. Only a few cases of lipoblastomas arising from the mesentery are reported in literature. We present a case of a rare giant lipoblastoma arising from the mesentery of a 6-year-old girl, with a history of postprandial abdominal pain.
巨大肠系膜脂肪母细胞瘤是一种罕见的起源于脂肪细胞的良性肿瘤。它可酷似恶性肿瘤,术前诊断困难。影像学检查有助于诊断但不能确诊。发生于腹部的那些肿瘤通常较大,可引起压迫症状。手术切除是首选的治疗方法,需要长期随访以检测局部复发情况。文献中仅报道了少数几例起源于肠系膜的脂肪母细胞瘤。我们报告一例罕见的起源于一名6岁女孩肠系膜的巨大脂肪母细胞瘤病例,该女孩有餐后腹痛病史。