Tao Chengpin, Cao Yongsheng
Pediatric Urology Department, Anhui Provincial Children's Hospital, Hefei, Anhui, People's Republic of China.
J Inflamm Res. 2024 Nov 27;17:9917-9923. doi: 10.2147/JIR.S499301. eCollection 2024.
Chylous effusion is a rare condition characterized by the accumulation of lymphatic fluid in body cavities, often due to trauma, malignancy, or congenital lymphatic abnormalities. The association of chylous effusion with a patent processus vaginalis (PV) in pediatric patients is exceptionally uncommon, presenting unique diagnostic and therapeutic challenges.
To report a rare case of bilateral patent processus vaginalis with chylous effusion in a pediatric patient, detailing the diagnostic process, surgical management, and outcomes, while contributing to the limited literature on this condition.
A 1-year-10-month-old male presented with a left inguinal-scrotal swelling. Ultrasonography suggested a hydrocele. Laparoscopic exploration revealed bilateral patent PVs with chylous fluid in the abdominal cavity and tunica vaginalis. The fluid was aspirated and analyzed, confirming chylous effusion. Bilateral high ligation of the PV was performed, and the patient was initially managed with a specialized diet.
The patient underwent successful laparoscopic bilateral high ligation of the PVs with complete resolution of symptoms. Follow-up ultrasonography at one week, one month, and three months post-surgery showed no evidence of fluid accumulation or hydrocele recurrence.
Bilateral patent processus vaginalis with chylous effusion is an extremely rare condition in pediatric patients. This case demonstrates that early surgical intervention with laparoscopic high ligation can effectively resolve the condition without the need for prolonged dietary modifications. Further documentation of similar cases is necessary to better understand and manage this rare clinical presentation.
乳糜性积液是一种罕见病症,其特征为体腔内淋巴液积聚,通常由创伤、恶性肿瘤或先天性淋巴异常引起。小儿患者中乳糜性积液与鞘状突未闭(PV)相关的情况极为罕见,带来了独特的诊断和治疗挑战。
报告一例小儿患者双侧鞘状突未闭合并乳糜性积液的罕见病例,详细阐述诊断过程、手术治疗及结果,同时为关于该病症的有限文献提供补充。
一名1岁10个月大的男性患儿出现左侧腹股沟阴囊肿胀。超声检查提示鞘膜积液。腹腔镜探查发现双侧鞘状突未闭,腹腔和鞘膜腔内有乳糜液。抽取液体进行分析,确诊为乳糜性积液。实施双侧鞘状突高位结扎术,患者最初采用特殊饮食进行管理。
患者成功接受腹腔镜双侧鞘状突高位结扎术,症状完全缓解。术后1周、1个月和3个月的随访超声检查显示无液体积聚或鞘膜积液复发迹象。
小儿患者双侧鞘状突未闭合并乳糜性积液是一种极其罕见的病症。该病例表明,腹腔镜高位结扎的早期手术干预可有效解决该病症,无需长期调整饮食。有必要进一步记录类似病例,以更好地理解和处理这种罕见的临床表现。