Left Lateral Sectionectomy
Anatomic resection of liver segments II and III, the most common minor anatomic hepatectomy, frequently performed laparoscopically for peripheral lesions and as donor procedure in pediatric living-donor liver transplantation.
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What is Left Lateral Sectionectomy?
Anatomy and indications: 1) Couinaud anatomy - left lateral section comprises segments II (superior, posterior) and III (inferior, anterior); supplied by left portal vein lateral branches and left hepatic artery; venous drainage via left hepatic vein; biliary drainage via left lateral hepatic duct; 2) Anatomic landmarks - falciform ligament marks medial border (umbilical fissure plane); umbilical fissure contains umbilical vein remnant (round ligament), portal venous structures; left hepatic vein lies posterior; 3) Indications - hepatocellular carcinoma in segments II/III in patients with adequate liver function (Child-Pugh A, ICG-R15 <15%); intrahepatic cholangiocarcinoma; colorectal liver metastases; symptomatic benign tumors (hemangioma >5 cm with symptoms, focal nodular hyperplasia >5 cm, adenoma >5 cm or any size in men); hepatolithiasis; living-donor liver transplantation for pediatric recipients (<10 kg); 4) Patient selection - assess hepatic function (Child-Pugh, MELD, future liver remnant volume), comorbidities, performance status; tumor characteristics (size, number, vascular invasion, extrahepatic disease, AFP level); MRI/CT for tumor staging and anatomic delineation; 5) Contraindications - decompensated cirrhosis, severe portal hypertension, advanced extrahepatic disease, distant metastases beyond resectability.
Surgical technique: 1) Approach - laparoscopic now standard (60-80% of LLS in high-volume centers; 4-5 ports; 30-degree scope; CO2 pneumoperitoneum 10-12 mmHg); robotic alternative; open via subcostal or upper midline incision for complex cases; 2) Steps - mobilization of left lateral section by division of round ligament, falciform ligament, left coronary ligament, left triangular ligament; intraoperative ultrasound for tumor localization and assessment of vascular structures; 3) Vascular control - dissection of umbilical fissure, identification and division of segments II and III portal pedicles (portal vein and hepatic artery branches with biliary duct using endo-GIA stapler or clips and division); selective inflow control reduces blood loss; 4) Parenchymal transection - along the umbilical fissure plane (left of falciform ligament), using ultrasonic dissector (CUSA), bipolar energy, harmonic scalpel, or stapler; control of vessels and biliary radicles within parenchyma; left hepatic vein controlled and divided at termination; 5) Specimen extraction - via slightly extended port, Pfannenstiel incision, or umbilical incision in laparoscopic; specimen placed in retrieval bag; 6) Hemostasis and closure - inspection of resection surface, argon beam coagulation, bipolar; closed-suction drain optional in selected cases; 7) Donor procedure variations - more meticulous dissection to preserve graft vascular and biliary anatomy; weight 200-300 g typical for pediatric recipient; intraoperative cholangiography essential.
Outcomes and postoperative care: 1) Operative time - laparoscopic 2-4 hours, open 2-3 hours; experienced surgeons; 2) Blood loss - laparoscopic 100-300 mL median, open 200-500 mL; transfusion rare in experienced hands (<10%); 3) Morbidity - overall 10-20%; bile leak 3-8% (most managed conservatively or endoscopically); pleural effusion 5-10%; intra-abdominal collection 3-5%; wound complications minimal in laparoscopic; 4) Mortality - <1% in experienced centers; 5) Length of stay - laparoscopic 3-5 days, open 5-7 days; 6) Postoperative care - early mobilization (day 1), oral intake (day 1-2), pain management with multimodal analgesia (avoid NSAIDs given hepatic considerations), DVT prophylaxis, monitor liver function tests, drain output if placed; 7) Oncologic outcomes - laparoscopic equivalent to open in oncologic outcomes (R0 resection rates, recurrence-free survival, overall survival); for HCC: 5-year survival 50-70% when performed in selected patients; 8) Living donor outcomes - donor mortality <0.1% in experienced pediatric LDLT programs; donor morbidity 10-20% mostly minor; full liver regeneration within 3 months; 9) Recurrence and surveillance - tumor markers (AFP, CEA, CA 19-9 as appropriate), CT/MRI every 3-6 months for first 2 years, then 6-12 months; treat recurrence as appropriate; 10) Functional outcome - rapid recovery; full activities by 4-6 weeks; pediatric donors typically return to school/activities in 2-4 weeks.
Symptoms
Risk Factors
When to See a Doctor?
If you experience any of the following symptoms, seek medical attention promptly:
- Liver mass on imaging requiring resection
- Elevated tumor markers (AFP, CEA)
- Pediatric LDLT donor evaluation
- Symptomatic benign liver lesion
- Persistent right upper quadrant pain
- Hepatolithiasis with cholangitis
Treatment Methods
Which Department to Visit?
You can visit our Genel Cerrahi department for these complaints. Our specialist physicians will create the most suitable treatment plan for you.
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