一个不寻常的原因,幼儿与大肚子,腹部淋巴畸形的病例报告

Lauren C. Riney
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摘要

腹痛是儿科急诊科(PED)最常见的主诉之一。由于潜在的诊断范围广泛,对幼儿的诊断、评估和治疗提出了挑战。一名3岁的健康女孩以腹痛、腹胀、食欲不振和近期体重增加就诊于我们的PED。体格检查是一个显著膨胀紧绷的腹部在其他方面表现良好的孩子正常的生命体征。初步评估发现贫血,炎症标志物升高,腹部超声(US)显示大量复杂的腹水,但腹膜内没有明确的肿块。我们咨询了儿科外科、儿科胃肠病学和儿科肿瘤学。腹部磁共振成像(MRI)显示大量腹腔内液体,内部复杂成分,未见可疑强化提示明显的恶性过程。她最终被诊断为先天性大网膜囊肿,需要切除和网膜切除术。病理表现为大囊性淋巴畸形。淋巴畸形是一种罕见的儿童病变,仅占儿童良性肿瘤的5%。常见部位包括颈部、腋窝,很少累及胃肠道。临床表现因肿瘤的大小和位置而异。由于诊断困难,许多人在生命后期出现。
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An unusual cause of a toddler with a big belly, abdominal lymphatic malformation case report
: Abdominal pain is one of the most common complaints seen in the pediatric emergency department (PED). Because of the broad range of potential diagnoses, it can pose challenges in the diagnostic evaluation and treatment in the young child. A 3-year-old previously healthy girl presented to our PED with abdominal pain, abdominal distention, poor appetite, and recent weight gain. Physical examination was notable for a significantly distended taut abdomen in an otherwise well appearing child with normal vital signs. Initial evaluation yielded anemia, elevated inflammatory markers, and an abdominal ultrasound (US) showing a large amount of complex intra-abdominal ascites without definite intra-peritoneal mass. Pediatric surgery, pediatric gastroenterology, and pediatric oncology were consulted. A magnetic resonance imaging (MRI) of the abdomen was performed and revealed a large amount of intraperitoneal fluid with a component of internal complexity and no suspicious enhancement to suggest overt malignant process. She was ultimately diagnosed with a large congenital omental cyst that required resection and omentectomy. Pathology was consistent with a macrocystic lymphatic malformation. Lymphatic malformations are uncommon pediatric lesions, accounting for only 5% of benign tumors in childhood. Common locations include the neck, axillae, and rarely involve the gastrointestinal tract. Clinical presentation varies depending on the size and location of the tumor. Many present later in life due to their diagnostic challenges.
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