小儿肝间质脂肪瘤--诊断难题

Manish Sahni, Ram Daga, Nishant Jangir, Suresh Singh, Rajgovind Sharma
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引用次数: 0

摘要

导言和重要性:肝脏良性肿瘤在儿童中较为罕见。间质脂肪瘤(MH)是一种肝脏良性肿瘤。它是仅次于婴儿血管瘤的第二常见的小儿肝脏良性肿瘤。多见于两岁以下儿童。由于临床症状无特异性,且缺乏明确的实验室检查,该肿瘤的诊断十分困难。我们在此介绍一例罕见的 2 岁间质火腿肠瘤患儿及其诊断难题。病例介绍:一名 2 岁的健康男童因肝脏肿块转诊至我院进行评估。他主诉自过去 10 周以来食欲不振、腹胀。他没有发烧/外伤的主诉。临床发现和检查:腹部检查发现肝脏肿大,无压痛,无转移性钝痛。放射学评估:腹部超声波检查显示单个右叶肿块。进一步的影像学检查显示,腹部 CT 扫描显示肝脏右叶有一个巨大的多发病灶,病灶内有动脉增强的间隔,病灶压迫并移位右门静脉和右肝静脉。病变压迫并移位右门静脉和右肝静脉。当时,实验室评估显示肝功能检查、血清甲胎蛋白和其他血液指标正常。鉴别诊断为肝囊肿、包虫囊肿和胆囊腺瘤。干预措施和结果:经过多学科讨论后,他被计划接受手术治疗,这也将为此类肝脏囊性病变提供确切的组织学诊断。他接受了最佳手术治疗,随后接受了右肝切除术,切除了约 14×12 厘米的肿块。没有出现严重的周围并发症,患者于 POD6 出院。切除肿块的病理检查显示,肿块内混有胆管、血管、不规则的肝细胞板和疏松的间质,其中含有大小不等的囊肿,与间质火腿肠瘤一致。定期随访时,他没有任何症状。相关性和影响:肝脏良性肿瘤在儿童中相对罕见。间质火腿肠瘤的诊断仍是一项挑战,因为它具有非特异性的主诉、正常的实验室检查结果,而且延误诊断会导致局部压迫引起并发症。虽然如果怀疑程度较高,先进的影像学检查可以诊断出这种肿瘤,但仅凭影像学检查很难将其与其他肿瘤(如未分化胚胎肉瘤)区分开来。因此,手术切除是诊断和治疗这类肿瘤的金标准。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Paediatric Mesenchymal Hamartoma of Liver-A Diagnostic Dilemma
Introduction and Importance: Benign tumors of the liver are relatively rare in children. Mesenchymal hamartoma (MH) is a benign tumor of the liver. It is the second most common benign pediatric hepatic tumor after infantile hemangioma. Mostly it is seen in children less than 2 years of age. The diagnosis of this tumor is difficult because of nonspecific clinical symptoms and lack of definitive laboratory studies. The precise diagnosis of mesenchymal hamartoma relies on histological evaluation of the tissue.We hereby present a rare case in a 2 year old child with mesenchymal hamartoma and its diagnostic challenges. Case presentation: A 2 year old previously healthy male was referred to our institution for evaluation of a liver mass. He complained of loss of apetite and abdominal distension since last 10 weeks. He had no complaints of fever/trauma. Clinical findings and Investigations: On per abdomen examination,there was a presence of large, non tender hepatomegaly with no shifting dullness present. On radiological evaluation, Ultrasound abdomen showed solitary right lobe mass. On further imaging, CT scan of the abdomen was done which showed a large multiloculated lesion in right lobe liver with arterial enhancing intervening septae within.The lesion was compressing and displacing right portal vein and right hepatic vein. At that time, laboratory evaluation showed normal liver function tests, serum AFP and other blood parameters. Differentials of liver cyst, hydatid cyst and biliary cystadenoma was made. Intervention and outcome: After discussion in multidisciplinary care, he was planned for surgery which would provide the exact histological diagnosis also in such cystic lesion of liver.He was optimized for surgery and subsequently underwent right hepatectomy with resection of the ~14× 12 cm mass. No major periperative complications developed and patient was discharged from hospital on POD6. The pathological review of the resected mass showed mixture of bile ducts, vessels, irregular liver cell plates and loose mesenchyme containing variable sized cysts consistent with a mesenchymal hamartoma. He is asymptomatic at the time of regular follow-up visits. Relevance and Impact: Benign tumors of the liver are relatively rare in children. The diagnosis of mesenchymal hamartoma still remains a challenge with non –specific complaints, normal laboratory findings and delay in diagnosis can lead to complications from local compression. Though advance imaging can diagnose this entity if index of suspicion is high but Differentiating it from other tumors such as an undifferentiated embryonal sarcoma is difficult on imaging alone. Hence surgical excision is the gold standard for diagnosing to reach the final histological diagnosis and treating these entities.
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