Добавил:
kiopkiopkiop18@yandex.ru t.me/Prokururor I Вовсе не секретарь, но почту проверяю Опубликованный материал нарушает ваши авторские права? Сообщите нам.
Вуз: Предмет: Файл:
Ординатура / Хирургия / Библиотека им академика М.И. Перельмана / Книга_1209_Библиотеки_им_академика_М_И_Перельмана.pdf
Скачиваний:
0
Добавлен:
15.09.2026
Размер:
17 Мб
Скачать
☆
22

Recommendations

• Symptomatic liver hemangiomas should be surgically resected if symptoms are
attributed to the hemangioma itself (evidence quality high, strong
recommendation).
• Asymptomatic giant hemangioma s can be safely observed regardless of tumor
size (evidence quality moderate, strong recommendation).
• The size of the hemangioma (greatest diameter) alone should not be used as an
indication for resection . (evidence quality moderate, strong recommendation)
• Rate of growth alone should not be used as an indication for surgical resection
(evidence quality low, weak recommendation).

References

1. Hoekstra LT, Bieze M, Erdogan D, Roelofs JJTH, Beuers UHW, van Gulik TM. Management
of giant liver hemangiomas: an update. Expert Rev Gastroenterol Hepatol. 2013;7:263.
2. Belghiti J, Cauchy F, Paradis V, Vilgrain V. Diagnosis and management of solid benign liver
lesions. Nat Rev Gastroenterol Hepatol. 2014;11:737–49.
3. Toro A, Mahfouz A-E, Ardiri A, et al. What is changing in indications and treatment of hepatic
hemangiomas. A review. Ann Hepatol. 2014;13:327.
4. Losanoff JE, Millis JM. Liver hemangioma complicated by obstructive jaundice. Am J Surg.
2008;196:e3.
5. Tang L, Zhou W-P. Education and imaging. Hepatobiliary and pancreatic: large cavernous
hemangioma with obstructive jaundice. J Gastroenterol Hepatol. 2009;24:930.
6. Kim DY, Pantelic MV, Yoshida A, Jerius J, Abouljoud MS. Cavernous hemangioma presenting
as Budd-Chiari syndrome. J Am Coll Surg. 2005;200:470.
7. Akbulut S, Yilmaz M, Kahraman A, Yilmaz S. Bilateral lower limb edema caused by compres-
sion of the retrohepatic inferior vena cava by a giant hepatic hemangioma. Int Surg. 2013;98:229.
8. Aydin C, Akbulut S, Kutluturk K, Kahraman A, Kayaalp C, Yilmaz S. Giant hepatic heman-
gioma presenting as gastric outlet obstruction. Int Surg. 2013;98:19.
9. Donati M, Stavrou GA, Donati A, Oldhafer KJ. The risk of spontaneous rupture of liver hem-
angiomas: a critical review of the literature. J Hepatobiliary Pancreat Sci. 2011;18:797–805.
10. Meguro M, Soejima Y, Taketomi A, et al. Living donor liver transplantation in a patient with
giant hepatic hemangioma complicated by Kasabach-Merritt syndrome: report of a case. Surg Today. 2008;38:463.
11. Ferraz AAB, Sette MJA, Maia M, et al. Liver transplant for the treatment of giant hepatic
hemangioma. Liver Trans. 2004;10:1436.
12. Vagefi PA, Klein I, Gelb B, et al. Emergent orthotopic liver transplantation for hemorrhage
from a giant cavernous hepatic hemangioma: case report and review. J Gastrointest Surg. 2011;15:209.
13. Giuliante F, Ardito F, Vellone M, et al. Reappraisal of surgical indications and approach for
liver hemangioma: single-center experience on 74 patients. Am J Surg. 2011;201:741.
14. Yedibela S, Alibek S, Müller V, et al. Management of hemangioma of the liver: surgical ther-
apy or observation? World J Surg. 2013;37:1303.
J. Seal
23
15. Yamagata M, Kanematsu T, Matsumata T, Utsunomiya T, Ikeda Y, Sugimachi K. Management
of haemangioma of the liver: comparison of results between surgery and observation. Br J Surg. 1991;78:1223.
16. Schnelldorfer T, Ware AL, Smoot R, Schleck CD, Harmsen WS, Nagorney DM. Management
of giant hemangioma of the liver: resection versus observation. J Am Coll Surg. 2010;211:724.
17. Pietrabissa A, Giulianotti P, Campatelli A, et al. Management and follow-up of 78 giant hae-
mangiomas of the liver. Br J Surg. 1996;83:915.
18. Herman P, Costa MLV, Machado MAC, et al. Management of hepatic hemangiomas: a 14-year
experience. J Gastrointest Surg. 2005;9:853.
19. Terkivatan T, Vrijland WW, Den Hoed PT, et al. Size of lesion is not a criterion for resection
during management of giant liver haemangioma. Br J Surg. 2002;89:1240.
20. Yoon SS, Charny CK, Fong Y, et al. Diagnosis, management, and outcomes of 115 patients
with hepatic hemangioma. J Am Coll Surg. 2003;197:392.
21. Charny CK, Jarnagin WR, Schwartz LH, et al. Management of 155 patients with benign liver
tumours. Br J Surg. 2001;88:808.
22. Mezhir JJ, Fourman LT, Do RK, et al. Changes in the management of benign liver tumours: an
analysis of 285 patients. HPB. 2013;15:156.
23. Weimann A, Ringe B, Klempnauer J, et al. Benign liver tumors: differential diagnosis and
indications for surgery. World J Surg. 1997;21:983.
24. Terkivatan T, de Wilt JW, de Man RA, et al. Indications and long-term outcome of treatment
for benign hepatic tumors: a critical appraisal. Arch Surg. 2001;136:1033.
25. Iwatsuki S, Todo S, Starzl TE. Excisional therapy for benign hepatic lesions. Surg Gynecol
Obstet. 1990;171:240.
26. Miura JT, Amini A, Schmocker R, et al. Surgical management of hepatic hemangiomas: a
multi-institutional experience. HPB. 2014;16:924.
27. Lerner SM, Hiatt JR, Salamandra J, et al. Giant cavernous liver hemangiomas: effect of opera-
tive approach on outcome. Arch Surg. 2004;139:818.
28. Longeville JH, de la Hall P, Dolan P, et al. Treatment of a giant haemangioma of the liver with
Kasabach-Merritt syndrome by orthotopic liver transplant a case report. HPB Surg. 1997;10:159.
29. Acharya M, Panagiotopoulos N, Bhaskaran P, Kyriakides C, Pai M, Habib N. Laparoscopic
resection of a giant exophytic liver haemangioma with the laparoscopic Habib 4× radiofre­quency device. World J Gastrointest Surg. 2012;4:199.
30. Gadiyaram S, Shetty N. Laparoscopic resection of giant liver hemangioma using laparoscopic
Habib probe for parenchymal transection. J Minim Access Surg. 2012;8:59.
31. Lanthaler M, Freund M, Nehoda H. Laparoscopic resection of a giant liver hemangioma.
J Laparoendosc Adv Surg Tech A. 2005;15:624.
32. Patriti A, Graziosi L, Sanna A, Gullà N, Donini A. Laparoscopic treatment of liver hemangi-
oma. Surg Laparosc Endosc Percutaneous Tech. 2005;15:359.
33. Giulianotti PC, Addeo P, Bianco FM. Robotic right hepatectomy for giant hemangioma in a
Jehovah’s witness. J Hepatobiliary Pancreat Sci. 2011;18:112.
34. Lupinacci RM, Szejnfeld D, Farah JFM. Spontaneous rupture of a giant hepatic hemangioma.
Sequential treatment with preoperative transcatheter arterial embolization and conservative hepatectomy. G Chir. 2011;32:469.
35. Panis Y, Fagniez PL, Cherqui D, Roche A, Schaal JC, Jaeck D. Successful arterial embolisa-
tion of giant liver haemangioma. Report of a case with fi ve-year computed tomography follow­ up. HPB Surg. 1993;7:141.
36. Suzuki H, Nimura Y, Kamiya J, et al. Preoperative transcatheter arterial embolization for giant
cavernous hemangioma of the liver with consumption coagulopathy. Am J Gastroenterol. 1997;92:688.
2 Is Surgery Indicated for Asymptomatic Giant Hepatic Hemangioma?
24
37. Vassiou K, Rountas H, Liakou P, Arvanitis D, Fezoulidis I, Tepetes K. Embolization of a giant
hepatic hemangioma prior to urgent liver resection. Case report and review of the literature. Cardiovasc Interv Radiol. 2007;30:800.
38. Zhou J-X, Huang J-W, Wu H, Zeng Y. Successful liver resection in a giant hemangioma with
intestinal obstruction after embolization. World J Gastroenterol. 2013;19:2974.
39. Gao J, Ke S, Ding X, Zhou Y, Qian X, Sun W. Radiofrequency ablation for large hepatic hem-
angiomas: initial experience and lessons. Surgery. 2013;153:78.
J. Seal
25© Springer International Publishing Switzerland 2016 J.M. Millis, J.B. Matthews (eds.), Diffi cult Decisions in Hepatobiliary and Pancreatic Surgery, Diffi cult Decisions in Surgery: An Evidence-Based Approach, DOI 10.1007/978-3-319-27365-5_3
Chapter 3
What Is the Best Surgical Method of Addressing Hepatic Hemangiomas?
J. Michael Millis and David Caba Molina
Abstract Hepatic hemangiomas are the most common benign tumor of the liver
and the second most common tumor following metastases. The diagnosis and man­agement of hepatic hemangiomas has improved signifi cantly for the past decade. The decision to treat this tumors surgically should be based mostly on symptomatol­ogy, inability to exclude malignancy, documented growth and less on feasibility for resection or patient anxiety. The decision for observation should be based on a thor­ough examination of asymptomatic tumors with benign characteristics on imaging. The surgical treatment of choice has evolved from formal hepatectomies to selected enucleation with improvement in outcomes regardless of the size of the lesion. Minimal invasive techniques have similar results as open surgery in appropriately selected patients with no difference in morbidity and mortality.
Keywords Hepatic hemangioma • Liver tumors • Enucleation

Introduction

Hepatic hemangiomas are the most frequent benign tumors of the liver with a fre­quency of 0.4–7.3 % in adults with a higher incidence in woman [ 1 – 3 ].
The accurate diagnosis of hemangiomas is a key component given the current high frequency of incidental fi ndings on CT scans that lead to further workup to differentiate malignant neoplasms from benign tumors. The most sensitive studies are MRI (100 %), CT scan (98.3) and US (96.9 %) [ 4 ].
The most common indications for the treatment of hemangiomas are abdominal pain , diagnostic uncertainty, enlargement, occupations and hobbies that may entail abdominal trauma and the extremely rare Kasabach-Merrit syndrome. The defi nition of “ giant hemangioma s” in the majority of the studies is a tumor with more than 4 cm in diameter [ 5 , 6 ].
J. M. Millis (*) • D. C. Molina Department of Surgery , University of Chicago Hospitals , MC 5027 , Chicago , IL 60637 , USA e-mail:
mmillis@surgery.bsd.uchciago.edu
26
There are four classic surgical methods of treatment for hepatic hemangiomas: liver resection , enucleation , hepatic artery ligation and liver transplant ation [ 7 ]. Enucleation refers to the creation of a plane between the normal liver parenchyma and the hemangioma without (or minimal) removal of normal hepatic parenchyma and it’s though to decrease blood loss, bile leak and preservation of parenchyma [ 8 ].
Newer adjuvants in the surgical treatment had emerged in the past decade includ­ing laparoscopic ultrasonic resection and supraselective arterial embolization , those techniques are used to increase safety of surgery [ 9 , 10 ]. Other non surgical treat- ments like radiotherapy , chemotherapy and transarterial embolization (TAE) had been proposed as successful alternatives when surgical resection is not indicated or feasible [ 11 – 13 ]. The resection can be achieved via an open or laparoscopic tech- nique and new technology like RFA has been used as part of the surgical minimal invasive category.

Search Strategy

An online literature search on English Language of publications from 2000 to 2014 was used to identify and select published data on the surgical management of hepatic hemangiomas using the PICO outline (Table 3.1 ).
The Databases used for the search were PubMed, Cochrane Evidence Based Medicine , MEDLINE-MEDLINE plus/OVID, Science Citation Index Expanded (SCI-EXPANDED). The terms used for the search were: “liver/hepatic hemangi­oma treatment” “surgical treatment of liver/hepatic hemangioma” “ management of liver/hepatic hemangioma” “ resection of/for hepatic hemangioma”, “treatment of liver/hepatic hemangioma”. The search was expanded to use articles that included or addressed hepatic hemangiomas as part of benign tumors of the liver since hem­angiomas tend to be clustered in that group as well, those terms include: “benign liver tumor s” “treatment of benign liver tumors” and “management of benign liver tumors”.
The studies showed were: Randomized controlled trials: 0, Retrospective cohort:
26.
Table 3.1 PICO table for surgical management of hepatic hemangiomas
P (Patients) I (Intervention) C (Comparator group)
Outcomes (Outcomes measured
Patients with diagnosed liver hemangioma (symptomatic or asymptomatic)
Surgical intervention (Open, Laparoscopic, mixed interventions with adjuvant treatment)
No surgical intervention ( observation) vs Surgical intervention ( enucleation vs hepatectomy, open vs Laparoscopic)
Perioperative complications
J.M. Millis and D.C. Molina
27

Results

Observation vs Surgical Treatment with Hepatectomy

The decision to treat hepatic hemangiomas surgically can be challenging when the indications are not well established and up to date guidelines are not encountered in the literature. Resection is indicated for symptoms and questionable diagnosis and the most widely methods studied are resection and enucleation [ 14 – 16 ].
A study from the University of Cincinnati from 2003 proposed an algorithm where the initial step is a triple phase CT , if there was any uncertainty of the diag­nosis of hemangioma a tagged RBC/MRI scan was obtained, if the lesion was asymptomatic observation would be granted and surgery was indicated in symptom­atic patients or increase in size along with large size hemangiomas. Ninety two percent of the entire series was properly diagnosed with this algorithm. Hemangiomas were 29 % of the cohort [ 17 ].
In 2001 Terkivatan et al. study aimed to prove that surgical treatment may not be justifi ed during long term follow up of patient with benign tumors of the liver. This study involved other benign liver tumor s and a total of 208 patients were analyzed of which 49.5 % (103) were hemagiomas and 24.2 % (25) of those patients under­went surgical resection . The main indication for resection in this subset of patients was abdominal pain (60 %) followed by suspected metastases. Non-anatomic resec­tion (40 %) and segmental resections (28 %) were the most common procedures utilized. In terms of postoperative morbidity 24 % (6) had a reportable complica­tion. The mean follow up for this group was 39 months. Of the conservative arm (non operative) a mean follow up of 45 months showed no mortality or coagulation, although there’s no mention on growth or increased pain in the follow up [ 18 ].
In a retrospective cohort at the University of Miami including benign and solid tumors of the liver seen over 14 years a total of 130 cases where treated, 55 % were hemangiomas (71 patients). Surgical excision was performed in 49 %. The morbidity was 5 %. No rupture or progression of symptoms was observed in the asymptomatic group, although the follow up details are not specifi ed in the study they concluded that resection in asymptomatic patients is not justifi ed no matter the size [ 3 ].
In 2003 Yoon et al . at MSKCC published a large series where only hemangiomas where included. A total of 115 patients in the 8 year cohort were analyzed, 45.3 % (52 patients) presented with symptoms (abdominal pain ) and underwent surgical resection , whereas 54.7 % (63) where observed. Inability to exclude malignancy was the indication in 29 %.
The median size of the resected group was 11 cm vs 4 cm unresected group, and of those more than half (58 %) had tumors larger than 10 cm. Enucleation was the treatment of choice in 60 %. Their complication rate was 25 %. In the observation arm only four patients had persistent symptoms without major complications [ 5 ].
In 2005 a paper from a group at the University of São Paolo presented a retro­spective series of 249 patients over 14 years. In this series 31.7 % patient were
3 What Is the Best Surgical Method of Addressing Hepatic Hemangiomas?
28
symptomatic. The paper made emphasis in conservative treatment, only 3.2 % (n = 8) were treated with surgery , the main indication was pain . Giant hemangiomas (>4 cm) were present in 27.4 % of the cohort. The mean follow up was 78 months without any complications in the observation arm [ 19 ].
In the Amsterdam experience a cohort of 34 patients were identifi ed and surgical resection was undertaken in 14 (41 %) after a mean follow up of 36.5 months due to progressive abdominal pain and suspected malignancy. Fifty eight percent of a group of tumors >5 cm underwent surgical treatment whereas in the group of smaller hemangiomas (<5 cm) only 20 %. The observation arm did not show any complications with a mean follow-up of 19.6 month [ 20 ].
A retrospective cohort from the Mayo Clinic in 2010 evaluated the rate of hemangioma- associated complications in patients with giant hemangioma s after clinical observation and after operative management to identify the optimal treat­ment algorithm. This series was based in a survey examination. A total of 233 patient (80.6 %) fell in the nonoperative group and 56 (19.4 %). Only 11 % of the nonopera­tive group had symptoms whereas 52 % on the operative group had abdominal pain . Nine percent of patient in the observation group developed symptoms or complica­tions after diagnosis . Of the operative arm 34 patients had partial hepatectomy (60.7 %), 22 patients underwent enucleation (1 laparoscopic ). The survey revealed that 93 % of patients undergoing surgery had good or better health status and there was no statistical signifi cant difference in the overall rate of adverse events between the two groups. The long term risk of adverse events associated with non operative management is similar to the short term risk of operative intervention.
Based on this study, prophylactic intervention independent of the size without any clinical indication is not recommended due to the potential life-threatening event (2 % nonoperative vs 7 % operative) [ 6 ].
Yedibela et al. in 2013 published a large series of patients undergoing observa­tion or surgical treatment of hemangiomas larger than >4 cm. A total of 103 patients underwent surgical resection mainly for abdominal pain (60 %). The indication for surgery in 51 % of asymptomatic patients was anxiety. There was resolution of symptoms in 88 % of patients. There was no statistical difference in the overall rate of adverse events between the surgical and observation group [ 21 ].

Enucleation vs Hepatectomy

In the year 2000 Özden published a study including 172 patients of which 42 underwent a surgical procedure for the treatment of hepatic hemangioma. Patients were evaluated to assess the effect of surgery ( enucleation using Pringle maneu­ver). Abdominal pain was the major indication for elective surgery, 78.5 % under­went enucleation followed by formal hepatectomy Early morbidity occurred in 12 % (5 patients) bleeding being the most common. A total of 33 patients (78 %) were followed for a median interval of 53 months, of those patients 96 % (32) were symptomatic prior the intervention. Complete resolution of pain was achieved in
J.M. Millis and D.C. Molina
29
88 % (24) of patients and US revealed no recurrences. The evaluation method was not well standardized and enucleation was favored as a safer technique by the authors [ 22 ].
At the University of Chicago a cohort of benign tumors of the liver included 28 patients with benign tumors 35.7 % being hemangiomas (10 patients) the most com­mon presenting symptom was pain and enucleation was performed in 64 % of patients. The complication rate was 10.7 % for the total cohort with no mention on hemangioma related complications [ 23 ].
A series from 2001 illustrated the changing indications for resection when patients are analyzed in a large cohort when indications changed (sixe, symptoms etc). This series included 57 patients undergoing resection for abdominal pain or size >4 cm, (criteria until 1996, cohort 1995–1999 after that only hemangiomas larger than 10 cm and pain were indications for surgery ). Sixty six percent their cases were enucleation as it was favored over the course of the cohort. Their com­plication rate was 10.4 % without any mortality . A recurrence occurred in 5.2 % of their patients (3 patients) [ 24 ].
Another series of 2001 demonstrated the relationship between tumor size and presence of symptoms, this series included 155 patient with benign liver tumor s, of which 63 % (97 patients) had been diagnosed with hemangiomas, 40 % of those patients underwent resection with the main indication being persistent symptoms (23 %). The majority (53 %) underwent enucleation , followed by segmentectomy (20 %). The median follow-up was 16 months and the series complication rate was 21 % [ 25 ].
A case series for giant cavernous hemangioma s including 52 patients was pub­lished to compare the outcomes on patients undergoing enucleation vs lobectomy. The series showed a higher complication rate with lobectomy (44 % vs 11 %), right lobe lesions more often treated with enucleation. Pringle fl ow occlusion was used far more frequently for enucleations (78 % vs 16 %). There was no statistical differ­ence in operative times and transfusions, although there was a trend towards improvement with enucleation [ 26 ].
The second study to compare enucleation versus hepatic resection was published in 2005. A cohort of 22 symptomatic patients underwent enucleation (n = 10) or formal liver resection (n = 12). The operative time was longer in the resection group and blood loss along with need for transfusion was also greater in the resection group with no effect in length of stay. The complication rate was 14.2 %. In this study tumor localization and number of hemangiomas were the factors for the selec­tion of surgery , being multiple and deep/central masses likely o have a formal resec­tion [ 27 ].
A small cohort of 21 patients published in the 2007 showed that patients under­going enucleation had less operative time (170 vs 230 min), blood loss (400 vs 1329 cc) and no morbidity with decreased length of hospital stay (5.6 vs 9.9 days) compared to liver resection . In this series the major indication were symptoms fol­lowed by uncertain diagnosis [ 28 ].
The approach for the surgical treatment with enucleation was addressed by the largest study available by Xiao-Hui regarding centrally of peripherally lesions and
3 What Is the Best Surgical Method of Addressing Hepatic Hemangiomas?
30
their respective outcomes , with the assumption that centrally located lesions (defi ned Couinaud’s segments I, IV, V and VII) are more challenging to resect. A total of 172 patients underwent enucleation with Pringle maneuver for pain , lesions larger than 10 cm or enlarging tumors. A total of 76 (44.2 %) were centrally located and 96 (55.8 %) were peripherally located. Enucleation of centrally located hemangiomas required signifi cantly longer vascular infl ow occlusion time (45.3 vs 32.6 min)lon­ger operating time (124.5 vs 89 min), higher volume of blood loss (800 vs 500 cc), greater blood transfusion (51 vs 42 pts, at least one unit of blood) and longer hospi­tal stay (10.2 vs 9.1). The morbidity was 2.9 % for the entire series with no differ­ence in the two groups, no mortality was registered. The median follow-up was 27 months and complete resolution of pain was achieved in 39.8 % and amelioration in 49.4 %.
This study is the only one to compare a crucial factor when deciding on resection of hemangiomas, the location of the hemangioma. As seen on previous papers, peripherally located lesions are more amenable for laparoscopic resection [ 8 ].
In 2011 a cohort of 74 patients was analyzed and were divided in two groups, for their management , operative (54.1 %) and nonoperative (45.9 %) with a median follow-up of 77.3 months. Abdominal pain was present in 37.8 % of the total cohort and in 62 % of the patients undergoing resection compared to 8.8 % in the nonop­erative group. The mean size of the lesions was larger in the operative group (11.9 vs 6 cm). A total of 28 formal liver resection s were made and 12 enucleations. This cohort includes a change after year 2000 when 50 % were resected by enucleations, size not being any different for enucleation vs formal resection. The decision was based on the location and the relationship with major vascular and biliary structures. The resection group had more pedicle clamping time than the enucleation subset, the rest of the intraoperative parameter did not show any statistical difference [ 29 ].

Minimal Invasive Approach

Minimal invasive techniques include laparoscopic and robotic resection with adju­vant technical instruments that facilitate the procedure [ 30 ].
One of the fi rst laparoscopic liver resection series of benign tumors was pub­lished in 2003 to asses the feasibility, safety and outcomes in a multicenter setting in 18 centers in Europe. In this series of 87 patients only 13 patients (15 %) corre­sponded to hemangiomas. The main indication for resection was pain an undeter­mined nature of atypical features. In the overall series 95 % of the tumors were located in the left lobe or anterior segments. For the hemangiomas almost 60 % of the lesions where localized in segments II and II with a median size of 6 cm with a 10 % conversion to open procedures (bleeding being the major cause, 45 %). The main procedures were wedge resection followed by segmentectomy and major hep­atectomy in three patients. Only one conversion was documented for a 13 cm hem­angioma [
31 ].
J.M. Millis and D.C. Molina
31
The fi rst paper to describe a series a laparoscopic radiofrequency ablation of hepatic hemangiomas consisted of 27 patients with symptomatic and rapid-growth lesions. A total of 50 liver lesions were treated successfully. There was a median follow up of 21 months without any complications. An intraoperative laparoscopic ultrasound was used prior and at completion of the ablation. An abdominal US and CT were performed 7 days and a moth after RFA . Follow up CT scans were obtained 3–6 months achieving 100 % necrosis and relieve of symptoms in about 85 % of patients [ 32 ].
The use of other technology as adjuvant in surgical treatment has been addressed in paper utilizing ultrasonically activated device in 12 patients (8 formal resections, 4 enucleations) was published with no mortality or morbidity [ 33 ].
A most recent study from Ho et al. addressed factors determining surgical out­comes . The series includes 61 patients undergoing resection for giant hemangioma s (>4 cm), postoperative complications were associated with larger tumors, symp­tomatic presentation, increased blood loss and operative time and greater use of intraoperative infl ow control. A Pringle maneuver was used in 50.8 %. The patients who had complications the majority had central tumors and required lobectomy. The complication rate was 4 % for enucleation and 19.4 % for resection [ 34 ].
A study by Yang et al. aimed to compare an important technical aspect of the surgical resection of hemangiomas, selective hepatic vascular exclusion (SHVE). A total of 273 patients had a hemangioma at least compressing one of the major hepatic veins from. Either SHVE (n = 120) or Pringle maneuver (n = 153) was used. No protocol was used for the selection. There was a signifi cant difference favoring SHVE in the following intraoperative data: Blood loss (600 vs 1,000), blood trans­fusion units (2 vs 4). Major blood loss of 2000 L only happened in the Pringle group and 85 % in this group did not undergo a blood transfusion compared to 76 % in the Pringle group, also there was no air embolism and no conversion to total hepatic vascular exclusion (7.2 % in the Pringle group). The operative time was longer in the SHVE group (139.8 vs 124.2) The overall complication rate was higher in the Pringle group (30.7 % vs 20.8 %) [ 35 ].
More recently Miura et al. described a retrospective review from six major liver centers in the US. A total of 241 patients underwent open surgery (mainly hepatec­tomy or segmentectomy) but 17 % had a laparoscopic approach, showing the ten­dency to adopt this technique. A total of 63.2 % of the patient undergoing surgery for symptoms had improvement. Complication rate was 14 % with improvement of symptoms in 63.2 % [ 36 ].
A summary of the major published reports describing the various surgical options for hepatic hemangiomas is provided in Table 3.2 .
3 What Is the Best Surgical Method of Addressing Hepatic Hemangiomas?