• Sana Viqar, ChandniChandni, Department of Pediatric Surgery, The Childrens Hospital, Pakistan Institute of Medical Sciences, Islamabad, Pakistan., and Muhammad Amjad Chaudhary.
• Sana Viqar, Department of Pediatric Surgery, The Childrens Hospital, Pakistan Institute of Medical Sciences, Islamabad, Pakistan.
• Pak J Med Sci. 2024 May 1; 40 (5): 103910411039-1041.

AbstractAbdominal cystic lymphangioma is a rare benign tumour in children. It is often difficult to diagnosis pre-operatively due to a varied spectrum of symptoms. We report a case of a male infant who presented with gross bilateral inguinoscrotal swelling. Provisional diagnosis of congenital communicating hydrocele was made and investigation revealed a large abdominal cyst. Patient underwent explorative laparotomy and the cyst arising from greater omentum, extending into bilateral scrotum, was excised and bilateral herniotomy done. Mass was confirmed to be lymphangioma on biopsy. This case is unique as an abdominal lymphangioma presented solely as inguinoscrotal swelling, with no abdominal symptom. To our knowledge, this is the first case of omental cystic lymphangioma involving both inguinoscrotal regions. Our case suggests that abdominal cystic lymphangioma should be a part of the differential diagnosis in any child with gross inguinoscrotal swelling in whom initial impression is of communicating hydrocele.Copyright: © Pakistan Journal of Medical Sciences.

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