Bilateral Lumbar Hernia - a Rare Occurence in Infant

S. Islam, A. Morshed, Md. Ashraf Ul Huq, M. Alam, S. Mondal, K. Hasina
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Abstract

Lumbar hernias are rare in children. We report a case of bilateral lumbar hernia in a 39 days old boy who was admitted at pediatric surgery department in Dhaka Medical College Hospital with the chief complaints of bilateral flank swellings since birth. There were no urinary or bowel complaints. Palpation revealed reducible, non-tender, soft to firm swellings involving iliolumbar region in left and lumbar region in right . These were increased on crying. On auscultation bowel sounds were present in left side and absent in right side. There were no other congenital anomalies.Ultrasonography revealed herniated bowel loops in left iliolumbar region and mild pelvicalicial dilatation in left kidney and slightly bigger right kidney in right lumbar region. On the basis of these findings a diagnosis of congenital bilateral lumbar hernias were made. Closer of the defects were done by prosthetic material and non- absorbable suture material. He came back for follow-up after 2 weeks, 4 weeks and 6 weeks. Defects were clinically absent and the patient was pain and recurrence-free. DOI: http://dx.doi.org/10.3329/jpsb.v1i2.19537
双侧腰疝——罕见的婴儿病例
腰疝在儿童中很少见。我们报告一例双侧腰椎疝在39天的男孩谁住在儿科外科在达卡医学院医院出生后的主要投诉双侧侧腹肿胀。没有尿路或肠道不适。触诊显示可复位,无触痛,软硬肿胀累及左侧髂腰区和右侧腰椎区。一哭这些就增加了。听诊左侧有肠音,右侧无。没有其他先天性异常。超声示左髂腰区肠袢突出,左肾轻度盆腔扩张,右腰区右肾略大。在这些发现的基础上诊断先天性双侧腰疝。修复材料和不可吸收缝线材料修复的缺损较多。术后2周、4周、6周随访。临床无缺陷,患者无疼痛和复发。DOI: http://dx.doi.org/10.3329/jpsb.v1i2.19537
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