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儿童腹腔内囊性肿块。

Cystic intra-abdominal masses in children.

作者信息

Ferrero Luisa, Guanà Riccardo, Carbonaro Giulia, Cortese Maria Grazia, Lonati Luca, Teruzzi Elisabetta, Schleef Jurgen

机构信息

Division of Pediatric General, Thoracic and Minimally Invasive Surgery, AOU Città della Salute e della Scienza, Regina Margherita Children's Hospital, Torino, Italy.

出版信息

Pediatr Rep. 2017 Oct 6;9(3):7284. doi: 10.4081/pr.2017.7284.

Abstract

Benign intra-abdominal cystic masses in infancy are fairly uncommon and their etiopathogenesis, histology and clinical presentation differ significantly. Our aim is to report our experience in their treatment in order to discuss the best diagnostic and treatment modality. The medical records of 5 children (2M, 3F) with cystic intraabdominal masses referred to our hospital between November 2012 and September 2016, were retrospectively reviewed. All patients underwent open surgery and subsequent histopathologic analysis. Different clinical presentations, localizations of the masses, diagnostic tools, surgical approaches, histological examinations and outcomes were reviewed. Patients mean age was 5.4 years (range: 8 months-9 years). Two patients presented recurrent abdominal pain and abdominal distension; 1 patient had a palpable mass discovered incidentally and 2 complained acute abdominal pain. Routine laboratory tests, tumor markers and abdominal ultrasound were immediately done in all patients. Three patients underwent MRI and 1 abdominal CT. At laparotomy 2 hepatic cysts, 2 mesenteric cyst and 1 retroperitoneal cyst were discovered. Histology reports described: 1 hepatobiliary cystadenoma, 1 benign hepatic hamartoma and 3 cystic lymphangiomas (1 retroperitoneal and 2 mesenteric). There were no major postoperative complications, deaths, or recurrences in our series (follow-up 3-24 months). Despite the rarity of these lesions, benign cystic abdominal masses in children are not so uncommon and should be considered as causes of acute abdominal pain. The differential diagnosis is not always possible preoperatively. In our series, radical excision of the lesions was possible in all cases, allowing reliable histological results and avoiding recurrences.

摘要

婴儿期良性腹腔内囊性肿块相当少见,其病因、组织学及临床表现差异显著。我们的目的是报告我们在其治疗方面的经验,以便探讨最佳的诊断和治疗方式。回顾性分析了2012年11月至2016年9月间转诊至我院的5例(2男,3女)腹腔内囊性肿块患儿的病历。所有患者均接受了开放手术及后续组织病理学分析。对不同的临床表现、肿块定位、诊断工具、手术方式、组织学检查及结果进行了回顾。患者平均年龄为5.4岁(范围:8个月至9岁)。2例患者表现为反复腹痛和腹胀;1例患者偶然发现可触及肿块,2例主诉急性腹痛。所有患者均立即进行了常规实验室检查、肿瘤标志物检测及腹部超声检查。3例患者接受了磁共振成像(MRI)检查,1例接受了腹部CT检查。剖腹探查发现2例肝囊肿、2例肠系膜囊肿和1例腹膜后囊肿。组织学报告显示:1例肝胆囊腺瘤、1例良性肝错构瘤和3例囊性淋巴管瘤(1例腹膜后,2例肠系膜)。我们的系列研究中无重大术后并发症、死亡或复发(随访3至24个月)。尽管这些病变罕见,但儿童良性腹腔囊性肿块并非十分少见,应被视为急性腹痛的病因。术前并非总能进行鉴别诊断。在我们的系列研究中,所有病例均可行病变的根治性切除,可获得可靠的组织学结果并避免复发。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/da8c/5643949/39d93c85a7a1/pr-9-3-7284-g001.jpg

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