Abstract
Patient: Female, 67-year-old
Final Diagnosis: Splenic hemangioma
Symptoms: Asymptomatic with progressive splenic lesion enlargement
Clinical Procedure: —
Specialty: Gastroenterology and Hepatology • Surgery
Objective: Rare disease
Background
Hemangioma is the most common benign primary tumor of the spleen and is often detected incidentally. Laparoscopic-assisted microwave ablation (LMWA) has recently been introduced as a novel approach for managing splenic hemangioma. This report describes the case of a 67-year-old woman with an asymptomatic, progressively enlarging splenic hemangioma successfully treated with LMWA.
Case Report
A 67-year-old woman was admitted for evaluation of a gradually enlarging splenic mass found during routine examination. She was asymptomatic, with normal tumor markers and a mildly elevated D-dimer level. Contrast-enhanced CT revealed a 6.0 cm hypervascular lesion in the upper pole of the spleen. After multidisciplinary discussion, LMWA was performed under direct laparoscopic visualization. The lesion was completely ablated, with a total operative time of 80 minutes, including 25 minutes of ablation. Estimated blood loss was minimal (20 mL). Postoperative pathology examination confirmed a splenic cavernous hemangioma. The postoperative course was uneventful, and she was discharged on day 5. Follow-up imaging showed reduction of the ablation zone to 5.4 cm, and laboratory results returned to normal.
Conclusions
This is the first report on the feasibility and safety of LMWA for treating splenic hemangioma. This approach effectively reduces intraoperative bleeding and postoperative hemolysis while preserving splenic function, offering a novel treatment option for splenic hemangioma.
Keywords: Ablation Techniques, General Surgery, Hemangioma, Laparoscopy, Spleen
Introduction
Splenic hemangioma is an uncommon lesion that occurs more often in women, with an estimated incidence of 0.02–0.16% [1,2]. Splenic hemangioma is still regarded as the most frequent benign tumor of the spleen. Most patients remain asymptomatic [3], but some have abdominal discomfort, diarrhea, or even respiratory problems [3]. Because of the unique structure of splenic tissue [4,5], percutaneous biopsy – while theoretically the diagnostic gold standard – is rarely undertaken in practice [6–10]. Instead, diagnosis is usually based on characteristic imaging findings, supplemented by laboratory tests when necessary. To date, there are no clinical practice guidelines or expert consensus statements that clearly define indications for treatment. Some investigators recommend intervention for lesions ≥4 cm [3,11,12], whereas others suggest using 5 cm as the cutoff [2,13].
Reported treatment options for splenic hemangioma include open splenectomy (OS), laparoscopic total splenectomy (LTS), laparoscopic partial splenectomy (LPS), and robot-assisted partial splenectomy (RAPS). LTS is commonly performed because it is minimally invasive [2,14,15]. However, since the spleen is critical to both innate and adaptive immunity [16–19], removing it completely greatly increases the risk of overwhelming post-splenectomy infection (OPSI), with mortality rates ranging from 50% to 80% [20–24]. In contrast, LPS and RAPS preserve splenic function but are technically demanding and often have longer operative times, greater blood loss, and higher costs [2,11,25]. At present, there is still no ideal approach that balances safety, minimal invasiveness, and preservation of spleen function.
Thermal ablation has gained increasing use in recent years for treatment of hepatic hemangioma (HH) [26–32], and is valued for its minimally invasive nature and rapid hemostatic effect. However, in giant hepatic hemangioma (GHH), reports of severe postoperative hemolysis and acute kidney injury (AKI) have become more frequent, which has limited its wider adoption [33]. The spleen, with its rich vascularity and essential roles in immunity and blood storage, is at even higher risk when ablation is attempted. Few publications have described the use of microwave ablation (MWA) to control bleeding at the residual splenic margin after laparoscopic partial splenectomy (LPS) [11,34], and no study has directly reported laparoscopic microwave ablation (LMWA) as a treatment for splenic hemangioma. Building on more than 2 decades of experience in tumor ablation and related research, our team developed a novel approach that combines LMWA with controlled phlebotomy. By creating small “gas-blood outflow channels” on the surface of the lesion, this technique reduces the amount of free hemoglobin (Hb) entering the circulation and markedly improves procedural safety. To the best of our knowledge, this is the first case report to describe LMWA for splenic hemangioma in detail, highlighting its feasibility, safety, and potential as a cost-effective, spleen-preserving treatment option.
Case Report
A 67-year-old woman was hospitalized for evaluation of a 2-year history of progressively enlarging splenic hemangioma. She was found to have a splenic hemangioma during a routine check-up in 2023, when the lesion measuring 3.7×3.8 cm. She had no symptoms at the time, such as abdominal pain or diarrhea. Follow-up imaging in 2024 showed that the lesion had grown to 5.2×4.3 cm, yet she remained symptom-free. Shortly before admission, an ultrasound revealed further enlargement, with the lesion reaching approximately 6.0 cm in diameter. She had no history of infectious diseases, such as hepatitis or malaria, no chronic conditions, no abdominal trauma, and no history of living abroad. She had no family history of splenic tumors. Results of the physical exam were normal.
The abdomen was soft and non-tender, with no rebound tenderness. Blood tests showed a D-dimer level of 572 ng/mL. Tumor markers – AFP, CA125, CA15-3, and CA72-4 – were all normal. The rest of the lab results were unremarkable. After admission, contrast-enhanced abdominal CT showed a large mass at the upper pole of the spleen with a distinctive ring of enhancement during the arterial phase (Figure 1A). The lesion became slightly denser in the venous phase and measured about 6.0×5.6 cm (Figure 1B). Before surgery, 3D reconstruction of the splenic hemangioma was performed, clearly revealing the origin of its feeding artery (Figure 1C). Enhanced CT showed a lesion with relatively slow enhancement and clear margins, and the patient had no symptoms, supporting a likely diagnosis of splenic hemangioma splenic hemangioma. Splenic lymphangiomas usually appear as multilocular cystic lesions, which were not seen in this case, making this diagnosis unlikely. Vascular malignancies of the spleen, such as angiosarcoma, tend to present as poorly defined masses with systemic symptoms like fever or weight loss; none of these were present, further lowering their likelihood. At admission, chest X-ray and preoperative tests, including tumor markers, were all normal, effectively ruling out metastatic disease. Postoperative paraffin pathology confirmed that the lesion was consistent with a splenic cavernous hemangioma, which was in accordance with the clinical diagnosis (Figure 2).
Figure 1. Preoperative imaging of splenic hemangioma patients.

(A) Enhanced ring at the edge of splenic hemangioma in arterial phase on enhanced CT (yellow arrow). (B) Slightly increased splenic hemangioma density in venous phase on enhanced CT (yellow arrow). (C) Source of splenic hemangioma feeding artery (white arrow) can be seen on three-dimensional reconstruction.
Figure 2. Splenic hemangioma (hematoxylin and eosin stain).
(A) 100× magnification. (B) 200× magnification. Note the typically dilated spaces lined by a bland endothelial monolayer.
We used a 2450 MHz microwave system (KY-2000 dual-source floor-standing; Kangyou Medical, China) for the procedure. This system includes 2 independent microwave generators, 2 flexible coaxial cables, and 2 water pumps, allowing simultaneous use of two 18-cm disposable microwave ablation needles with 1.5-cm antenna tips and cooling shafts. Each generator can deliver power between 1 and 100 W. An experienced hepatobiliary surgeon performed the procedure according to the preoperative plan. An MWA equipment operator monitored urine color changes in real time during the operation and manually controlled the ablation time as needed.
After anesthesia was successfully induced, the patient was placed in a supine position with the right arm abducted, head elevated, feet lowered, and upper body tilted to the left. Percutaneous ultrasonography revealed a hemangioma at the upper pole of the spleen, measuring approximately 6 cm in diameter. A 1-cm incision was made just below the umbilicus, through which a Veress needle was inserted to establish pneumoperitoneum. Once adequate insufflation was achieved, a 10-mm trocar was introduced, followed by the insertion of a 30° laparoscope into the abdominal cavity. Dense adhesions were found between the upper pole of the spleen and the lateral wall of the stomach. A localized exophytic splenic hemangioma was identified. A 5-mm trocar was placed just below the left costal margin, slightly inferior to the xiphoid midline, and a 12-mm trocar was positioned symmetrically on the right side (Figure 3).
Figure 3. Laparoscopic port placement.

Port 1: disposable suction device, placed at the right midclavicular line. Port 2: laparoscope, placed at the anterior midline. Port 3: Cadiere forceps, placed at the left anterior axillary line.
A disposable suction device was inserted, and the left lateral lobe of the liver was lifted. The ligaments connecting the stomach and spleen were carefully separated to expose the upper pole of the spleen. A 6-cm exophytic splenic hemangioma was seen, surrounded by abundant blood vessels. Under direct laparoscopic visualization, a needle biopsy of the splenic hemangioma was performed as part of the LMWA procedure. The tissue specimen was promptly processed for routine paraffin-embedded histopathological examination. Using laparoscopic guidance and intraoperative ultrasound, 2 disposable ablation electrodes (KY-450B-T7) were placed at the bases of the splenic hemangioma’s upper and lower poles and were secured to prevent movement (Figure 4A). Gentle pressure was applied to the splenic hemangioma surface with the suction device to temporarily reduce blood flow in the communicating vessels. Electrode positions were checked again with ultrasound, and the power was gradually increased to perform the ablation step by step (Figure 4B).
Figure 4. Key steps in the laparoscopic microwave ablation procedure.

(A) The MWA needle is inserted at the lower edge of the splenic hemangioma. (B) After repositioning and ablation, hemolyzed blood drains from the splenic hemangioma (white arrow). (C) During ablation, the hemolyzed blood is removed with a suction device.
After the first ablation, the electrode was repositioned for a second ablation to ensure complete treatment of the splenic hemangioma. Ultrasound was used throughout to monitor the heat-irrigate effect (HIE) in the lesion and surrounding spleen, as well as to observe changes in spleen color. Gentle pressure was applied to the spleen surface with a disposable suction device to aspirate blood containing damaged red blood cells leaking from the puncture site of the initial ablation (Figure 4C). Once ablation was complete, the electrode was removed, and bleeding at the puncture site was controlled. The area was thoroughly flushed with normal saline, bleeding was checked again, laparoscopic instruments were withdrawn, and the incision was closed with absorbable subcutaneous sutures (YA-2021Q). The entire procedure lasted 80 minutes, including 25 minutes of ablation, with an estimated blood loss of 20 mL.
During surgery and on the first day after, 125 mL of 5% NaHCO3 solution was given to alkalize the urine, along with adequate fluids and diuretics (furosemide). Blood counts, liver and kidney function, urine tests, coagulation (Figure 5A), IL-6, and PCT were checked on days 1, 2, and 3 after surgery. Although inflammatory markers (IL-6, PCT) went up right after surgery, they dropped significantly as the patient steadily recovered (Figure 5B, 5C). AST levels rose briefly after the operation but returned to normal by day 3, platelet levels fell briefly but also returned to normal by day 3, and postoperative renal function levels remained essentially normal (Figure 5D–5F).
Figure 5.
Postoperative laboratory test results.
We used the Clavien-Dindo classification to categorize complications related to splenic hemangioma treatment [35]. These typically include pleural effusion, pancreatic fistula, wound and lung infections, splenic abscess, postoperative bleeding, and acute kidney injury. The patient developed hemoglobinuria (HbU) 24 hours after surgery, but urine occult blood tests were negative by 48 hours. No serious complications occurred after LMWA.
Before discharge, an enhanced abdominal CT scan showed an ablation area about 5.7×5.5 cm in size, with no enhancement ring visible around the edge of the splenic hemangioma lesion during the arterial phase (Figure 6A, 6B). The patient was discharged on the fifth day after surgery.
Figure 6. Postoperative imaging of patient with splenic hemangioma.
(A, B) Pre-discharge contrast-enhanced CT, no arterial phase rim enhancement. (C, D) Upper-abdominal magnetic resonance imaging at 6 months after ablation, showing no splenic hemangioma recurrence.
At 6 months after the procedure, she remained symptom-free and had no complications related to thermal ablation. Follow-up contrast-enhanced magnetic resonance imaging (MRI) of the upper abdomen showed no new splenic hemangioma lesions, and the ablation area had shrunk to 3.83×3.52 cm (Figure 6C, 6D).
Discussion
Splenic hemangioma is the most common benign splenic tumor [36,37]. Most patients are asymptomatic [38,39], but some have abdominal discomfort. Spontaneous rupture is rare (1 of 31 reported cases [3.2%]) [1,40]. Larger splenic hemangioma can cause compression, affect coagulation, and, in severe cases, lead to Kasabach-Merritt syndrome.
There are currently no established guidelines for managing splenic hemangioma [2]. Some experts suggest considering surgery for lesions 4 cm or larger [41], while others use 5 cm as the threshold [2,13]. Treatment options include medication, transarterial embolization (TAE), surgical resection, and thermal ablation [42]. OS has traditionally been the mainstay, but LTS has gradually become the preferred approach [44,45] since was first reported in 1992 [43]. However, total splenectomy is often difficult to justify for benign disease because the spleen plays a crucial role in immunity [22,46,47]. Studies show that preserving as little as 25% of splenic tissue is enough to maintain normal immune function [2,16,48,49], which has led to growing interest in spleen-preserving procedures such as LPS and RAPS, but spleen-preserving surgery still has challenges. First, if the splenic hemangioma is supplied by multiple splenic arteries, the procedure can be technically demanding, especially laparoscopically, and the risk of intraoperative rupture and bleeding increases. Second, patients with Kasabach-Merritt syndrome often have coagulopathy, making hemostasis on the remaining spleen more difficult and raising the risk of hemorrhagic shock. Third, for larger splenic hemangiomas, spleen-preserving surgery does not always offer clear advantages over total splenectomy and can result in longer operation times, more postoperative pain, and extended hospitalization [44,50].
Thermal ablation has been used with some success on the residual splenic surface for hemostasis [11,34], but there are still no case reports of it being used as a definitive treatment for splenic hemangioma. The main challenge is the spleen’s rich blood supply and large blood volume. Studies show that heating red blood cells to 60°C for 5 minutes causes significant hemolysis, releasing large amounts of cell-free Hb [51], which can result in hemoglobinuria (HbU) and, in severe cases, AKI. Controlling this postoperative hemolytic response remains a major barrier to using thermal ablation in splenic hemangioma. Furthermore, evidence suggests that radiofrequency ablation (RFA) carries a higher risk of hemolysis than MWA, making MWA a more promising option [29,52].
Building on our experience with HH, we have developed an innovative approach using LMWA combined with a “blood release” technique for treating splenic hemangioma. Unlike percutaneous ultrasound-guided microwave ablation (UMWA), LMWA allows direct, real-time visualization of the ablation zone, avoids ultrasound artifacts, and prevents delayed needle tract bleeding. We also create a small “gas-blood outflow channel” on the splenic hemangioma surface, which enables damaged blood cells to drain into the abdominal cavity during ablation, reducing the release of cell-free Hb into the circulation and lessening the hemolytic response. Importantly, the splenic feeding arteries are first ablated to reduce tumor blood flow, which shortens ablation time and improves procedural safety.
The coagulated area seen after ablation does not indicate residual or recurrent disease, but is composed of inactivated splenic hemangioma tissue. This thermal effect differs from simple coagulative necrosis; over time, the ablated tissue gradually shrinks and eventually stabilizes once it reaches a certain size [53].
This report has several limitations. First, as a case report and literature review, its small sample size calls for further validation through multi-center, large-scale clinical trials. Second, the safety of LMWA relies heavily on the surgeon’s understanding of key principles such as HIE [54], heat-sink effect (HSE), heat-conductive effect (HCE), and oven effect (OE). Junior surgeons, in particular, need to build a solid foundation in these techniques to ensure safe and effective application.
Conclusions
This is the first report of the feasibility and safety of LMWA for treating splenic hemangioma. This approach effectively reduces intraoperative bleeding and postoperative hemolysis while preserving splenic function, offering a novel treatment option for splenic hemangioma.
Acknowledgements
We sincerely thank all the staff who contributed to this study, whose dedication and teamwork made its successful completion possible.
The authors thank the editor and series editor for constructive criticisms of an earlier version of this manuscript.
Footnotes
Financial support: This study was supported by a grant from the National Natural Science Foundation of China (52273256)
Conflict of interest: None declared
Institution Where Work Was Done: The First Medical Center of PLA General Hospital, Beijing, PR China.
Pateint Consent: Written informed consent was obtained from the patient prior to participation in this study.
Declaration of Figures’ Authenticity: All figures submitted have been created by the authors who confirm that the images are original with no duplication and have not been previously published in whole or in part.
References
- 1.Lin JL, Lin C, Wang HL, et al. Splenic artery embolization and splenectomy for spontaneous rupture of splenic hemangioma and its imaging features. Front Cardiovasc Med. 2022;9:925711. doi: 10.3389/fcvm.2022.925711. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Xue HM, Chen P, Zhu XJ, et al. Robot-assisted partial splenectomy for benign splenic tumors: Four case reports. World J Clin Oncol. 2024;15(10):1366–75. doi: 10.5306/wjco.v15.i10.1366. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 3.Kolekar S, Chincholi T, Kshirsagar A, Patankar R. Giant splenic hemangioma in a 10-year-old boy treated with a spleen saving surgery. J Surg Case Rep. 2017;2017(11):rjx217. doi: 10.1093/jscr/rjx217. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Tam A, Krishnamurthy S, Pillsbury EP, et al. Percutaneous image-guided splenic biopsy in the oncology patient: An audit of 156 consecutive cases. J Vasc Interv Radiol JVIR. 2008;19(1):80–87. doi: 10.1016/j.jvir.2007.08.025. [DOI] [PubMed] [Google Scholar]
- 5.Lieberman S, Libson E, Maly B, et al. Imaging-guided percutaneous splenic biopsy using a 20- or 22-gauge cutting-edge core biopsy needle for the diagnosis of malignant lymphoma. Am J Roentgenol. 2003;181(4):1025–27. doi: 10.2214/ajr.181.4.1811025. [DOI] [PubMed] [Google Scholar]
- 6.McInnes MDF, Kielar AZ, Macdonald DB. Percutaneous image-guided biopsy of the spleen: Systematic review and meta-analysis of the complication rate and diagnostic accuracy. Radiology. 2011;260(3):699–708. doi: 10.1148/radiol.11110333. [DOI] [PubMed] [Google Scholar]
- 7.Keogan MT, Freed KS, Paulson EK, et al. Imaging-guided percutaneous biopsy of focal splenic lesions: Update on safety and effectiveness. Am J Roentgenol. 1999;172(4):933–37. doi: 10.2214/ajr.172.4.10587123. [DOI] [PubMed] [Google Scholar]
- 8.Lucey BC, Boland GW, Maher MM, et al. Percutaneous nonvascular splenic intervention: A 10-year review. Am J Roentgenol. 2002;179(6):1591–96. doi: 10.2214/ajr.179.6.1791591. [DOI] [PubMed] [Google Scholar]
- 9.Singh AK, Shankar S, Gervais DA, et al. Image-guided percutaneous splenic interventions. Radiographic. 2012;32(2):523–34. doi: 10.1148/rg.322115135. [DOI] [PubMed] [Google Scholar]
- 10.Patel N, Dawe G, Tung K. Ultrasound-guided percutaneous splenic biopsy using an 18-G core biopsy needle: Our experience with 52 cases. Br J Radiol. 2015;88(1055):20150400. doi: 10.1259/bjr.20150400. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Chen Z, Liu Z. Application of microwave ablation in laparoscopic partial splenectomy. J Vis Exp. 2024;(213):e67563. doi: 10.3791/67563. [DOI] [PubMed] [Google Scholar]
- 12.Reyes-Jaimes L, Camacho-Aguilera JF. [Spontaneous splenic rupture. Case report and literature review]. Rev Medica Inst Mex Seguro Soc. 2023;61(4):523–31. doi: 10.5281/zenodo.8200591. [in Spanish] [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Chin EH, Shapiro R, Hazzan D, Katz LB, Salky B. A ten-year experience with laparoscopic treatment of splenic cysts. JSLS. 2007;11(1):20–23. [PMC free article] [PubMed] [Google Scholar]
- 14.Birindelli A, Martin M, Khan M, et al. Laparoscopic splenectomy as a definitive management option for high-grade traumatic splenic injury when non operative management is not feasible or failed: A 5-year experience from a level one trauma center with minimally invasive surgery expertise. Updat Surg. 2021;73(4):1515–31. doi: 10.1007/s13304-021-01045-z. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 15.Rosin D, Brasesco O, Rosenthal RJ. [Laparoscopic splenectomy: New techniques and indications]. Chirurg. 2001;72(4):368–77. doi: 10.1007/s001040051317. [in German] [DOI] [PubMed] [Google Scholar]
- 16.Van Wyck DB, Witte MH, Witte CL. Compensatory spleen growth and protective function in rats. Clin Sci Lond Engl 1979. 1986;71(5):573–79. doi: 10.1042/cs0710573. [DOI] [PubMed] [Google Scholar]
- 17.Liu G, Fan Y. Feasibility and safety of laparoscopic partial splenectomy: A systematic review. World J Surg. 2019;43(6):1505–18. doi: 10.1007/s00268-019-04946-8. [DOI] [PubMed] [Google Scholar]
- 18.Bing Y, Sadula A, Xiu D, Yuan C. Laparoscopic middle segment splenectomy for central splenic hemangioma: A case report. Int J Surg Case Rep. 2020;77:925–29. doi: 10.1016/j.ijscr.2020.10.098. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 19.King H, Shumacker HB. Splenic studies. I. Susceptibility to infection after splenectomy performed in infancy. Ann Surg. 1952;136(2):239–42. doi: 10.1097/00000658-195208000-00006. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Theilacker C, Ludewig K, Serr A, et al. Overwhelming postsplenectomy infection: A prospective multicenter cohort study. Clin Infect Dis. 2016;62(7):871–78. doi: 10.1093/cid/civ1195. [DOI] [PubMed] [Google Scholar]
- 21.Nardo-Marino A, Brousse V. Splenectomy in sickle cell disease: Do benefits outweigh risks? Haematologica. 2023;108(4):954–55. doi: 10.3324/haematol.2022.281587. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 22.Di Sabatino A, Carsetti R, Corazza GR. Post-splenectomy and hyposplenic states. Lancet Lond Engl. 2011;378(9785):86–97. doi: 10.1016/S0140-6736(10)61493-6. [DOI] [PubMed] [Google Scholar]
- 23.Buesing KL, Tracy ET, Kiernan C, et al. Partial splenectomy for hereditary spherocytosis: A multi-institutional review. J Pediatr Surg. 2011;46(1):178–83. doi: 10.1016/j.jpedsurg.2010.09.090. [DOI] [PubMed] [Google Scholar]
- 24.Zheng L, Deng C, Li J, et al. Treatment of hemangioma of the spleen by preoperative partial splenic embolization plus laparoscopic partial splenectomy: A case report. Medicine (Baltimore) 2018;97(17):e0498. doi: 10.1097/MD.0000000000010498. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 25.Nyilas Á, Paszt A, Simonka Z, et al. [Laparoscopic splenectomy in our practice at the University of Szeged Department of Surgery]. Magy Sebeszet. 2022;75(2):200–7. doi: 10.1556/1046.2022.20017. [in Hungarian] [DOI] [PubMed] [Google Scholar]
- 26.Zhang HL, Meng HB, Li XL, et al. Laparoscopy-guided percutaneous microwave ablation for symptomatic 12.8 cm hepatic hemangioma with low blood loss and short hospital stay post-operation: A case report and literature review. Clin Hemorheol Microcirc. 2021;77(2):165–71. doi: 10.3233/CH-200922. [DOI] [PubMed] [Google Scholar]
- 27.Wang LZ, Wang KP, Mo JG, et al. Minimally invasive treatment of hepatic hemangioma by transcatheter arterial embolization combined with microwave ablation: A case report. World J Clin Cases. 2021;9(24):7154–62. doi: 10.12998/wjcc.v9.i24.7154. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 28.Tang X, Ding M, Lu B, et al. Outcomes of ultrasound-guided percutaneous microwave ablation versus surgical resection for symptomatic large hepatic hemangiomas. Int J Hyperthermia. 2019;36(1):632–39. doi: 10.1080/02656736.2019.1624837. [DOI] [PubMed] [Google Scholar]
- 29.Fei L, Hongsong X. Effectiveness of microwave ablation for the treatment of hepatic hemangioma – meta-analysis and meta-regression. Int J Hyperthermia. 2023;40(1):2146214. doi: 10.1080/02656736.2022.2146214. [DOI] [PubMed] [Google Scholar]
- 30.Chen L, Zhang L, Tian M, et al. Safety and effective of laparoscopic microwave ablation for giant hepatic hemangioma: A retrospective cohort study. Ann Med Surg 2012. 2019;39:29–35. doi: 10.1016/j.amsu.2019.02.001. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 31.Shi Y, Song J, Ding M, et al. Microwave ablation versus transcatheter arterial embolization for large hepatic hemangiomas: Clinical outcomes. Int J Hyperthermia. 2020;37(1):938–43. doi: 10.1080/02656736.2020.1766122. [DOI] [PubMed] [Google Scholar]
- 32.Liu F, Yu X, Liang P, et al. Ultrasonography-guided percutaneous microwave ablation for large hepatic cavernous haemangiomas. Int J Hyperthermia. 2018;34(7):1061–66. doi: 10.1080/02656736.2017.1392045. [DOI] [PubMed] [Google Scholar]
- 33.Kacała A, Dorochowicz M, Patrzałek D, et al. Safety and feasibility of transarterial bleomycin-lipiodol embolization in patients with giant hepatic hemangiomas. Medicina (Kaunas) 2023;59(8):1358. doi: 10.3390/medicina59081358. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Zhang Q, Tian Y, Duan J, et al. 915 MHz microwave-assisted laparoscopic partial splenectomy: A case series. J Minimal Access Surg. 2020;16(4):441–44. doi: 10.4103/jmas.JMAS_32_19. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 35.Katayama H, Kurokawa Y, Nakamura K, et al. Extended Clavien-Dindo classification of surgical complications: Japan Clinical Oncology Group postoperative complications criteria. Surg Today. 2016;46(6):668–85. doi: 10.1007/s00595-015-1236-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Ramani M, Reinhold C, Semelka RC, et al. Splenic hemangiomas and hamartomas: MR imaging characteristics of 28 lesions. Radiology. 1997;202(1):166–72. doi: 10.1148/radiology.202.1.8988207. [DOI] [PubMed] [Google Scholar]
- 37.Knott EM, Valusek PA, St Peter SD. Laparoscopic excision of a giant splenic vascular tumor. J Pediatr Surg. 2012;47(7):E21–23. doi: 10.1016/j.jpedsurg.2012.03.054. [DOI] [PubMed] [Google Scholar]
- 38.Islam S, Newman EA, Strouse PJ, Geiger JD. Antiangiogenic therapy for a large splenic hemangioma. Pediatr Surg Int. 2005;21(12):1007–10. doi: 10.1007/s00383-005-1533-3. [DOI] [PubMed] [Google Scholar]
- 39.Willcox TM, Speer RW, Schlinkert RT, Sarr MG. Hemangioma of the spleen: Presentation, diagnosis, and management. J Gastrointest Surg. 2000;4(6):611–13. doi: 10.1016/s1091-255x(00)80110-9. [DOI] [PubMed] [Google Scholar]
- 40.Glusman ZA, Webb JJ. Use of point-of-care ultrasound to diagnose a ruptured splenic hemangioma. Cureus. 2024;16(7):e63698. doi: 10.7759/cureus.63698. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Choi W, Choi YB. Splenic embolization for a giant splenic hemangioma in a child: A case report. BMC Pediatr. 2018;18(1):354. doi: 10.1186/s12887-018-1331-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Hkyung Shim, Kim MR. Potassium-titanyl-phosphate (KTP) laser photocoagulation combined with resection using an ultrasonic scalpel for pharyngolaryngeal hemangioma via a transoral approach: Case report and literature review. Am J Case Rep. 2021;22:e931402. doi: 10.12659/AJCR.931042. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 43.Hashizume M, Sugimachi K, Ueno K. Laparoscopic splenectomy with an ultrasonic dissector. N Engl J Med. 1992;327(6):438. doi: 10.1056/NEJM199208063270621. [DOI] [PubMed] [Google Scholar]
- 44.Costi R, Castro Ruiz C, Romboli A, et al. Partial splenectomy: Who, when and how. A systematic review of the 2130 published cases. J Pediatr Surg. 2019;54(8):1527–38. doi: 10.1016/j.jpedsurg.2018.11.010. [DOI] [PubMed] [Google Scholar]
- 45.Lee SH, Lee JS, Yoon YC, Hong TH. Role of laparoscopic partial splenectomy for tumorous lesions of the spleen. J Gastrointest Surg. 2015;19(6):1052–58. doi: 10.1007/s11605-015-2812-5. [DOI] [PubMed] [Google Scholar]
- 46.Crary SE, Buchanan GR. Vascular complications after splenectomy for hematologic disorders. Blood. 2009;114(14):2861–68. doi: 10.1182/blood-2009-04-210112. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 47.Casciani F, Trudeau MT, Vollmer CM. Perioperative immunization for splenectomy and the surgeon’s responsibility: A review. JAMA Surg. 2020;155(11):1068–77. doi: 10.1001/jamasurg.2020.1463. [DOI] [PubMed] [Google Scholar]
- 48.Kimura K, Kurashima Y, Tanaka K, et al. Laparoscopic partial splenectomy for splenic lymphangioma: A case report. Surg Case Rep. 2020;6(1):140. doi: 10.1186/s40792-020-00882-1. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Li Q, Liu Z, Hu M, et al. Laparoscopic partial splenectomy of benign tumors assisted by microwave ablation. J Cancer Res Ther. 2020;16(5):1002–6. doi: 10.4103/jcrt.JCRT_816_19. [DOI] [PubMed] [Google Scholar]
- 50.Lazaar H, Malki Y, Bouhout T, et al. Partial splenectomy for a sizeable cavernous hemangioma: Case report and a review of the literature. Cureus. 2021;13(1):e12882. doi: 10.7759/cureus.12882. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 51.Chong CCN, Lee KF, Cheung SYS, et al. Prospective double-blinded randomized controlled trial of Microwave versus RadioFrequency Ablation for hepatocellular carcinoma (McRFA trial) HPB. 2020;22(8):1121–27. doi: 10.1016/j.hpb.2020.01.008. [DOI] [PubMed] [Google Scholar]
- 52.Kong J, Gao R, Wu S, et al. Correction to: Safety and efficacy of microwave versus radiofrequency ablation for large hepatic hemangioma: A multicenter retrospective study with propensity score matching. Eur Radiol. 2022;32(5):3615. doi: 10.1007/s00330-022-08634-5. [DOI] [PubMed] [Google Scholar]
- 53.Ahmed M, Solbiati L, Brace CL, et al. Image-guided tumor ablation: Standardization of terminology and reporting criteria – a 10-year update. Radiology. 2014;273(1):241–60. doi: 10.1148/radiol.14132958. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Jiang K, Chen J, Liu Y, et al. Heat-irrigate effect’ of radiofrequency ablation on relevant regional hepatocyte in living swine liver-initial study on pathology. Cell Biochem Biophys. 2015;72(1):37–41. doi: 10.1007/s12013-014-0398-2. [DOI] [PubMed] [Google Scholar]



