Abstract

Cystic lymphangioma is a benign congenital malformation of the lymphatic vessels. At the National Center for Pediatric Surgery, Gezira State, Sudan; 2021; a female baby of 15 months old age presented complaining of abdominal distention of 10 days duration. Patient Looks unwell, not febrile, and not pale or jaundice; abdomen was distended with full flanks, there was a palpable mass in the epigastric region, no area of tenderness and no palpable organs. Abdomino-pelvic U/S showed very huge abdomino –pelvic cystic mass with multiple thick septa. CT abdomen showed huge abdomino-pelvic mass with multiple cysts that having variable sizes measuring up to 6*7 cm. An elective explorative laparotomy was done. Intra operative findings: Multiple cystic masses arise from the root of the small bowel mesentery matted together with multiple enlarged mesenteric lymph nodes involving segment of distal jejunum with multiple adhesions. Release of adhesion, resection of the masses along with 57 cm of the involving jejunum, anastomosis was done, and homeostasis was secured. Histopathology result showed dilated cystic spaces; lined by flat endothelial cells and multiple reactive lymph nodes, no evidence of malignancy. Features are in line with lymphangioma and associated mesenteric lymphadenitis. Discussion and Conclusion: Our case was 15 months old which is the age of presentation as mentioned internationally. Mesenteric cystic Lymphangiomas are more common among male unlike our case. Ultrasonography and CT abdomen were highly recommended to achieve early diagnosis and treatment of such cases.

Highlights

  • Cystic lymphangioma is a benign congenital malformation of the lymphatic vessels

  • Features are in line with lymphangioma and associated mesenteric lymphadenitis

  • Mesenteric cystic Lymphangiomas are more common among male unlike our case

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Summary

Introduction

Cystic lymphangioma is a benign congenital malformation of the lymphatic vessels. It is due to lack of lymphatic vascular connections; as a result of a developmental defect in the lymphatic system that leads to a sequestration of the lymphatic tissue. Lymphangiomas are a group of vascular hamartomas, which result from a developmental failure in the vascular system, including lymphatic and/or arteries and veins. MCL represents 5–6% of benign tumors among children It occurs more in boys than girls (5:2) with a mean age at presentation of 2 years. Cystic change can result from any obstruction formed by hemorrhagic or an inflammatory process in the lymphatic vessels [2, 8, 11]. Patients usually present with abdominal pain, abdominal distension, palpable abdominal mass, nausea, vomiting, early satiety, and alteration in bowel habits These features are related to the cyst dimensions, localizations and relation to the surrounding tissues [2, 5, 8, 10, 14,15,16, 18]. Surgical excision should be complete for the whole involved part to achieve excellent prognosis; incomplete excision can lead to recurrence [2,3,4, 6, 10, 11, 13, 18]

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