Laparoscopic Excision of an Abdominal Lymphatic Malformation
Educational content from recorded physician discussions — not medical advice. Talk to your (or your child's) care team about your situation.
Video
Pediatric Surgical Oncology Research Collaborative (PSORC): Studying Rare Pediatric Tumors
56 s · Published May 2026
Video
Update Course Rewind 2025: Hirschsprung + ARM: Rare but Real
1 min · Published May 2026
Video
Update Course Rewind 2025: Hirschsprung + ARM: Rare but Real
1 min · Published May 2026
Video
Pooling Patients to Study Rare Pediatric Tumors: An Introduction to PSORC
56 s · Published May 2026
Video
The fetal frontier: A review of current and emerging fetal therapies for genetic diseases
44 s · Published May 2026
Video
Indocyanine green assists with sentinel lymph node mapping in pediatric and adolescent patients
1 min · Published May 2026
What the experts said
The lymphatic malformation arose from the mesentery of the gastric lesser curvature.
Initial ultrasound and CT scan demonstrated a large cystic mass thought to be of adnexal origin extending into the upper abdomen.
Initial laparoscopic exploration supported the presumptive diagnosis of a cystic mass arising from the pelvis.
Further manipulation demonstrated non-pelvic origin with normal adnexa.
The mass was connected by a torsed pedicle traveling over the transverse colon through the greater omentum.
An omental origin was initially suspected but further dissection demonstrated the omentum to be simply adherent to the torsed pedicle and not the source of it.
The mass was discovered to be connected to another large cyst attached to the gastric wall, extending posterior to the stomach into the lesser sac.
A ligature device was used to separate the mass from the gastric wall and gastric mesentery.
Following excision, the greater curvature was completely intact and uninvolved.
The mass arose from the lesser curvature mesentery and occupied the lesser sac.
The stomach was tested for leak after installation of dilute methylene blue through the nasogastric tube, and none was identified.
The mass was easily removed through the 10 millimeter umbilical port.
The patient was started on oral intake a few hours after the operation and discharged the following day.
All symptoms resolved postoperatively.
A screening ultrasound one year after excision showed no recurrence.
Lymphatic malformation was diagnosed grossly and histologically.
Had this lesion been approached by a Pfannenstiel incision, a correct diagnosis and excision would not have been possible without a second laparotomy incision.
Abdominal lymphatic malformations can be discovered incidentally or become acutely symptomatic due to torsion, hemorrhage, rupture, or sudden enlargement.