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巨大原发性网膜囊肿:儿童假性腹水和鞘膜积液的罕见病因。

Giant primary omental cyst: an unusual cause of pseudoascites and hydrocele in a child.

作者信息

Mohamed Hanan Youssif, Joya Habib Ullah, Alansari Amani N

机构信息

Pediatric Surgery Department, Benghazi Medical Center, Benghazi District 8606891, Sha'biyat Region, Libya.

Department of Pediatric Surgery, Hamad Medical Cooperation, Doha 2001, Qatar.

出版信息

J Surg Case Rep. 2024 Dec 12;2024(12):rjae774. doi: 10.1093/jscr/rjae774. eCollection 2024 Dec.

Abstract

Abdominal lymphangiomas are benign congenital abnormal dilatation and proliferation of lymphatic spaces primarily seen in children. The wide spectrum of symptoms challenges preoperative diagnoses. We present a rare case of a 2-year-old boy presented to pediatrician with massive abdominal distention and left scrotal swelling since the age of 1½ years. Diagnosed and treated as ascites, the patient was referred to pediatric surgery for ascitic tap and hydrocele repair. An abdominal CT scan revealed a giant omental cyst. Laparotomy was performed to excise the cyst extending into left scrotum, and deep left inguinal ring was closed from within. Lymphangioma was histopathologically confirmed. To the best of our knowledge to date, only one case of an omental cystic lymphangioma presenting as bilateral hydroceles without abdominal symptoms has been reported. Nevertheless, this case is unique for the presentation of pseudoascites and a unilateral hydrocele.

摘要

腹部淋巴管瘤是一种主要见于儿童的良性先天性淋巴管腔异常扩张和增生。其广泛的症状给术前诊断带来挑战。我们报告一例罕见病例,一名2岁男孩自1.5岁起出现腹部巨大膨隆和左侧阴囊肿胀,就诊于儿科医生处。该患者最初被诊断为腹水并接受相应治疗,后因腹水穿刺和鞘膜积液修复被转诊至小儿外科。腹部CT扫描显示为一个巨大的网膜囊肿。行剖腹手术切除延伸至左侧阴囊的囊肿,并从内部封闭左侧腹股沟深环。组织病理学确诊为淋巴管瘤。据我们目前所知,仅有一例网膜囊性淋巴管瘤表现为双侧鞘膜积液且无腹部症状的病例报道。然而,该病例因出现假性腹水和单侧鞘膜积液而独具特色。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a2e4/11635821/1d9833b0752a/rjae774f1.jpg

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