巨大原发性网膜囊肿:导致儿童假性筋膜囊肿和鞘膜积液的不寻常原因。

IF 0.4 Q4 SURGERY
Journal of Surgical Case Reports Pub Date : 2024-12-12 eCollection Date: 2024-12-01 DOI:10.1093/jscr/rjae774
Hanan Youssif Mohamed, Habib Ullah Joya, Amani N Alansari
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引用次数: 0

摘要

腹部淋巴管瘤是一种先天性淋巴管异常扩张和增生的良性肿瘤,主要见于儿童。淋巴管瘤的症状多种多样,给术前诊断带来挑战。我们报告了一例罕见病例,一名两岁男孩因腹部胀大和左侧阴囊肿胀就诊于儿科医生。患者被诊断为腹水并接受了治疗,随后被转诊至小儿外科进行腹水穿刺和鞘膜积液修补术。腹部 CT 扫描发现了一个巨大的网膜囊肿。腹腔镜手术切除了延伸至左侧阴囊的囊肿,并从内部封闭了左侧腹股沟深环。淋巴管瘤经组织病理学证实。据我们所知,迄今为止,只有一例网膜囊性淋巴管瘤表现为双侧水肿而无腹部症状的报道。然而,本病例的独特之处在于其表现为假性囊肿和单侧水囊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant primary omental cyst: an unusual cause of pseudoascites and hydrocele in a child.

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.

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来源期刊
CiteScore
0.70
自引率
0.00%
发文量
559
审稿时长
11 weeks
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