CASE REPORT article

Front. Oncol., 13 July 2022

Sec. Surgical Oncology

Volume 12 - 2022 | https://doi.org/10.3389/fonc.2022.873338

Case Report: Rare Acute Abdomen: Focal Nodular Hyperplasia With Spontaneous Rupture

  • YS

    Ying Si 1

  • BS

    Bo Sun 2

  • TZ

    Ting Zhao 1

  • KX

    Ke Xiao 1

  • DZ

    Dong-Xia Zhao 1

  • YH

    Yong-Mao Huang 1*

  • 1. Department of Infectious Diseases, The Affiliated Hospital of Southwest Medical University, Luzhou, China

  • 2. Department of Ultrasound, The Affiliated Hospital of Southwest Medical University, Luzhou, China

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Abstract

Focal nodular hyperplasia (FNH) of the liver is a benign lesion characterized by hypertrophic nodules with central star-shaped fibrous scars. The etiology and pathogenesis of FNH are not completely understood. A 43-year-old man was hospitalized because of acute abdominal pain. Emergency computed tomography(CT) showed hepatic tumor rupture and bleeding. The patient’s condition improved following arteriographic embolization to stop bleeding. Laparotomy confirmed spontaneous rupture and hemorrhage of focal hyperplasia and the patient remains asymptomatic after an uneventful recovery. FNH with spontaneous rupture and bleeding is extremely rare. Currently, there is no unified management standard for FNH and most previous studies recommend observation and follow-up. We recommend consideration of surgical treatment of cases with spontaneous rupture and bleeding.

Introduction

Focal nodular hyperplasia (FNH) is the second most common benign liver tumor and accounts for approximately 8% of all primary hepatic tumors. It is thought to be a hyperplastic response to increased blood flow in an arterial malformation rather than a true neoplasm (1, 2). Spontaneous hemorrhage of an FNH is very rare, and only 10 cases have been reported (3). This patient with spontaneous rupture and bleeding of a FNH in the right liver was successfully treated by second step surgical treatment.

Case presentation

A 43-year-old Chinese man was admitted to the hospital because of acute abdominal pain. He had no history of trauma, was in good health, and had been an intermittent alcohol user for about 20 years. Physical examination revealed no palpable mass or tenderness in the right upper abdomen. Blood routine showed that Hemoglobin was 142g/L.Alanine aminotransferase(502.6/U/L)and aspartate aminotransferase(527.9/U/L)were significantly increased. Blood coagulation tests and tumor-marker levels were normal. Abdominal enhanced computed tomography (CT) showed a round, approximately8.0cm×8.0cm mass with a slightly blurred border in the right lobe of the liver, and blood around the liver. A tumor hemorrhage was suspected (Figure 1) and as continued bleeding could not be ruled out, the patient underwent hepatic arteriographic embolization in the emergency department. Intraoperative angiographic findings the tumor was stained in irregular mass, with irregular outer border and widened perihepatic shadow. During the operation, lipiodol and gelatin sponge particles were used to embolize the responsible blood supply artery of the tumor. Re-imaging after embolization showed that the imaging of tumor supplying arteries was significantly reduced, the tumor staining range was significantly reduced, and the embolic agent was well deposited and the patient’s condition improved after 2 weeks of conservative treatment. After preoperative and intraoperative evaluation, the patient underwent right hemihepatectomy. Intraoperative exploration revealed that most of the tumor was located in segment VII and VIII, and a small part was located in segment V, adjacent to the right hepatic artery. Tumor size is about 8.0cm×8.0cm cm with an incomplete capsule, the boundary was clear, and an old blood accumulation was seen around the liver. The resected tumor was round, with clear boundaries and contained a hematoma. Pathologic examination of hematoxylin–eosin-stained tissue showed hepatocyte proliferation and vasodilation, and no atypical hyperplasia (Figures 2). Immunohistochemistry showed focally positive CK19 and CD34 cells consistent with capillary formation (Figures 3). The pathological features resulted in a final diagnosis of FNH with spontaneous rupture and bleeding. The patient recovered uneventfully and remains asymptomatic for 2 years. Figure 4, 5, 6

Figure 1

Figure 2

Figure 3

Figure 4

Figure 5

Figure 6

Discussion

FNH is the second most prevalent benign liver tumor after hepatic cavernous hemangioma. The incidence is highest in those 20–50 years of age, but FNH can occur at any age (4, 5). It most often occurs in women of childbearing age with a history of oral contraceptives (6, 7). The etiology is not fully understood, but vascularization by an anomalous artery, reactive hyperplasia after hepatocellular injury induced by vasculitis, or aberrant, increased blood flow have been implicated (8–10).

Previous cases of FNH with intraperitoneal hemorrhage, including this patient, reported in English-language publications are shown in Table 1 (3, 14–20). This review reviewed 11 patients, including 2 males and 9 females. The incidence was mainly female, with an average age of 31.7 years. As most FNH patients have no symptoms, most lesions are found by accident. Most symptomatic patients present with abdominal pain, discomfort in the right upper abdomen, and nausea. Very few have palpable masses (21–26). Liver enzyme values are abnormal in the serum of 10% to 14% of patients (27).Abdominal ultrasound, CT, and magnetic resonance imaging (MRI) with radioactive labels may reveal star scars (28).MRI has higher sensitivity and specificity for diagnosis of FNH than CT and abdominal ultrasound, especially magnetic resonance cholangiopancreatography (29, 30). Contrast-enhanced ultrasound with sonazoid may provide hemodynamic information of the vascular pattern and Kupffer-phase imaging improves diagnostic confidence and is effective for follow-up in clinical practice (31).

Table 1

First author (year)Age (years)/sexDiameter (mm)LocationNoImaging findingsTreatmentOutcome(Refs.)
Mays ET(1974)26/F100Right lobe1NRSurgeryNR(11)
Becker YT(1995)18/F45Right lobe2NRSurgeryNR(12)
Hardwigsen J(2001)37/F50Right lobe1NRSurgeryNR(13)
Bathe OF(2003)27/F60Right lobe1HHAFSurgeryAlive/18 mo(14)
Rahili A(2005)35/F98Lobus caudatus1HHAFSurgeryAlive/78 mo(15)
Chang SK(2005)42/F100Right lobe1HHAFSurgeryNR(16)
Demarco MP(2006)37/F52Left lobe4HHAFSurgeryNR(17)
Li T (2006)26/F150Left robeNRHHAFSurgeryAlive/8 mo(18)
Yajima D(2013)23/F10Right lobe1NRRevealed at autopsyDead(19)
Kinoshita M (2016)35/M80Right lobe1HHAFSurgeryAlive/48 mo(3)
Present study (2020)43/M80Right lobe1HHAFSurgeryAlive/to date(-)

Documented patients of hemorrhage caused by FNH.

M, male; F, female; mo, months; No, number; HHAF, high-density hematoma area formed; NR, not reported.

The occurrence of spontaneous rupture and bleeding of FNH might be explained as follows: Bleeding in FNH patients may be the result of vascular malformations and intratumoral pressure associated (2, 9, 10). Increased intratumoral pressure compresses the malformed blood vessels, eventually leading to results in spontaneous bleeding. For this patient, he had a history of alcoholic hepatitis, and the liver tissue was fragile. The tumor was located around the liver and adjacent to the right hepatic artery and was large and vulnerable to external force. Therefore, the combined effect of the above factors may have caused the rupture of the tumor.

Nguye et al. (32) described FNH as having two pathologies classical and non-classical. Non-classical FNH includes telangiectasia, mixed hyperplasia, and adenoma-like characteristics. Classical FNH accounts for the vast majority of diagnoses. Fabre et al. (33) proposed FNH histology scoring criteria including four main characteristics (fibrous elements, thick-walled blood vessels, hyperplastic small bile ducts, and nodules) and two minor characteristics (dilatation of liver blood sinuses and sinus fibrosis). FNH can be diagnosed if three of the four main characteristics, two main characteristics, and one or two minor characteristics are present. The presence of two or fewer major characteristics does not support a diagnosis of FNH. FNH currently has no specific immunohistochemical markers. CK19 and CK56 are markers of liver precursor cells and bile duct epithelium and CK7 is a marker of immature hepatocytes. The combined use of CK7 and CK19 is helpful for the diagnosis of FNH. CD34 is a marker of vascular endothelium, and because dilated arteries with thick walls or cavernous hemangioma occur in FNH lesions, CD34 staining is often positive. CD19 is a membrane antigen associated with cell proliferation. FNH is a local vascular malformation of the liver with increased perfusion that results in abnormal proliferation of local hepatocytes and formation of nodular lesions. Therefore, CD19 staining is often positive. There are reports in the literature that β-catenin can activate glutamine synthetase (GS), which results in typical map-like staining. Therefore, GS staining may assist in the diagnosis of FNH (34, 35).

At present, there is no consensus on the standard treatment of FNH, which is a benign lesion with no underlying malignancy. Most recommendations are for follow-up of asymptomatic patients (36). Surgery is the mainstay of treatment for patients with symptoms, enlarged lesions, and imaging indeterminate lesions during follow-up. Rupture and bleeding of liver tumors is a life-threatening condition. Emergency arteriographic embolization of unexplained hepatic mass hemorrhage can successfully control bleeding in 99% of patients (13). After the patient’s condition improves, the second-stage mass can be removed and the condition diagnosed. In our experience, combined first-stage interventional embolization and second-stage mass resection can be used as the standard treatment for FNH rupture and bleeding.

Conclusion

Spontaneous rupture and bleeding of FNH is very rare, but should be fully considered in patients who experience sudden abdominal pain during follow-up.

Publisher’s Note

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article, or claim that may be made by its manufacturer, is not guaranteed or endorsed by the publisher.

Statements

Data availability statement

The original contributions presented in the study are included in the article/Supplementary Material. Further inquiries can be directed to the corresponding author.

Ethics statement

Written informed consent was obtained from the participant for the publication of this case report.

Author contributions

YS wrote all drafts. BS discussed the meaning of the draft. TZ and KX collect all the references. D-XZ carried out the pathology and collected the clinical data. Y-MH offered conception and finalized the draft. All authors read and approved the final manuscript.

Conflict of interest

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Abbreviations

FNH, Focal nodular hyperplasia; CT, Computed tomography; MRI, magnetic resonance imaging; CEUS, contrast-enhanced ultrasound; GS, glutamine synthetase; RFA, radiofrequency ablation; TAE, transarterial embolization; PVA, polyvinyl alcohol.

References

  • 1

    VilgrainV. Focal Nodular Hyperplasia. Eur J Radiol (2006) 58(2):236–45. doi: 10.1016/j.ejrad.2005.11.043

  • 2

    OldhaferKJHabbelVHorlingKMakridisGWagnerKC. Benign Liver Tumors. Visceral Med (2020) 36(4):292–303. doi: 10.1159/000509145

  • 3

    KinoshitaMTakemuraSTanakaSHamanoItoGAotaTet al. Ruptured Focal Nodular Hyperplasia Observed During Follow-Up: A Case Report. Surg Case Rep (2017) 3(1):44. doi: 10.1186/s40792-017-0320-4

  • 4

    PekliDKokasBBárdosDFülöpAPajorPHahnOet al. A Focalis Nodularis Hyperplasia Multimodális Kezelése. Orvosi Hetilap (2022) 163(15):606–12. doi: 10.1556/650.2022.32439

  • 5

    AssyNNasserGDjibreABeniashviliZEliasSZidanJ. Characteristics of Common Solid Liver Lesions and Recommendations for Diagnostic Workup. World J Gastroenterol (2009) 15(26):3217–27. doi: 10.3748/wjg.15.3217

  • 6

    HermanPPuglieseVMachadoMAMontagniniALSalemMZBacchellaTet al. Hepatic Adenoma and Focal Nodular Hyperplasia: Differential Diagnosis and Treatment. World J Surg (2000) 24(3):372–6. doi: 10.1007/s002689910059

  • 7

    PainJAGimsonAEWilliamsRHowardER. Focal Nodular Hyperplasia of the Liver: Results of Treatment and Options in Management. Gut (1991) 32(5):524–7. doi: 10.1136/gut.32.5.524

  • 8

    ChioreanLCuiXWTannapfelAFrankeDStenzelMKosiakWet al. Benign Liver Tumors in Pediatric Patients - Review With Emphasis on Imaging Features. World J Gastroenterol (2015) 21(28):8541–61. doi: 10.3748/wjg.v21.i28.8541

  • 9

    Franchi-AbellaSBranchereauS. Benign Hepatocellular Tumors in Children: Focal Nodular Hyperplasia and Hepatocellular Adenoma. Int J Hepatol (2013) 2013:215064. doi: 10.1155/2013/215064

  • 10

    European Association for the Study of the Liver (EASL). EASL. Clinical Practice Guidelines on the Management of Benign Liver Tumours. J Hepatol (2016) 65(2):386–98. doi: 10.1016/j.jhep.2016.04.001

  • 11

    HsuehKCFanHLChenTWChanDCYuJCTsouSSet al. Management of Spontaneously Ruptured Hepatocellular Carcinoma and Hemoperitoneum Manifested as Acute Abdomen in the Emergency Room. World J Surg (2012) 36(11):2670–6. doi: 10.1007/s00268-012-1734-6

  • 12

    MaysETChristophersonWMBarrowsGH. Focal Nodular Hyperplasia of the Liver. Possible Relationship to Oral Contraceptives. Am J Clin Pathol (1974) 61(6):735–46. doi: 10.1093/ajcp/61.6.735.

  • 13

    BeckerYTRaifordDSWebbLWrightJKChapmanWCPinsonCW. Rupture and Hemorrhage of Hepatic Focal Nodular Hyperplasia. Am Surg (1995) 61(3):210–4. doi: 00000478-199503000-00018.

  • 14

    HardwigsenJPonsJVeitVGarciaSLe TreutYP. A Life-Threatening Complication of Focal Nodular Hyperplasia. J Hepatol (2001) 35(2):310–2. doi: 10.1016/S0168-8278(01)00096-4

  • 15

    BatheOFMiesCFranceschiDCasillasJLivingstoneAS. Massive Hemorrhage and Infarction Complicating Focal Nodular Hyperplasia of the Liver. HPB (Oxford) (2003) 5(2):123–6. doi: 10.1080/13651820310000

  • 16

    RahiliACaiJTrastourCJuwidABenchimolDZhengMet al. Spontaneous Rupture and Hemorrhage of Hepatic Focal Nodular Hyperplasia in Lobus Caudatus. J Hepatobiliary Pancreat Surg (2005) 12(2):138–42. doi: 10.1007/s00534-004-0936-1

  • 17

    ChangSKChungYFThngCHLooHW. Focal Nodular Hyperplasia Presenting as Acute Abdomen. Singapore Med J (2005) 46(2):90–2.

  • 18

    DemarcoMPShenPBradleyRFLevineEA. Intraperitoneal Hemorrhage in a Patient With Hepatic Focal Nodular Hyperplasia. Am Surg (2006) 72(6):555–9. doi: 10.1177/000313480607200620

  • 19

    LiTQinLXJiYSunHCYeQHWangLet al. Atypical Hepatic Focal Nodular Hyperplasia Presenting as Acute Abdomen and Misdiagnosed as Hepatocellular Carcinoma. Hepatol Res (2007) 37(12):1100–5. doi: 10.1111/j.1872-034X.2007.00164.x

  • 20

    YajimaDKondoFNakataniYSaitohHHayakawaMSatoYet al. A Fatal Case of Subcapsular Liver Hemorrhage in Late Pregnancy: A Review of Hemorrhages Caused by Hepatocellular Hyperplastic Nodules. J Forensic Sci (2013) 58 Suppl 1:S253–7. doi: 10.1111/j.1556-4029.2012.02246.x

  • 21

    GuttmacherAEMarchukDAWhiteRIJr. Hereditary Hemorrhagic Telangiectasia. N Engl J Med (1995) 333(14):918–24. doi: 10.1056/NEJM199510053331407

  • 22

    BuscariniEDanesinoCPlauchuHde FazioCOlivieriCBrambillaGet al. High Prevalence of Hepatic Focal Nodular Hyperplasia in Subjects With Hereditary Hemorrhagic Telangiectasia. Ultrasound Med Biol (2004) 30(9):1089–97. doi: 10.1016/j.ultrasmedbio.2004.08.004

  • 23

    ScardapaneAFiccoMSabbàCLorussoFMoschettaMMaggialettiNet al. Hepatic Nodular Regenerative Lesions in Patients With Hereditary Haemorrhagic Telangiectasia: Computed Tomography and Magnetic Resonance Findings. Radiol Med (2013) 118(1):1–13. doi: 10.1007/s11547-012-0789-3

  • 24

    BonneyGKGomezDAl-MukhtarAToogoodGJLodgeJPPrasadR. Indication for Treatment and Long-Term Outcome of Focal Nodular Hyperplasia. HPB (Oxford) (2007) 9(5):368–72. doi: 10.1080/13651820701504173

  • 25

    HseeLCMcCallJLKoeaJB. Focal Nodular Hyperplasia: What are the Indications for Resection? HPB (Oxford) (2005) 7(4):298–302. doi: 10.1080/13651820500273624

  • 26

    ShawcrossDLNaoumovNPachiadakisIMamaisCWilliamsRJalanRet al. Should a Biopsy Precede Liver Resection or Transplantation for Presumed Hepatocellular Carcinoma When the Alfa Fetoprotein is Normal? Transplantation (2004) 77(4):637–8. doi: 10.1097/01.TP.0000109783.98513.E3

  • 27

    FiooleBKokkeMvan HillegersbergRRinkesIH. Adequate Symptom Relief Justifies Hepatic Resection for Benign Disease. BMC Surg (2005) 5:7. doi: 10.1186/1471-2482-5-7

  • 28

    GrazioliLMoranaGFederleMPBrancatelliGTestoniMKirchinMAet al. Focal Nodular Hyperplasia: Morphologic and Functional Information From MR Imaging With Gadobenate Dimeglumine. Radiology (2001) 221(3):731–9. doi: 10.1148/radiol.2213010139

  • 29

    BiezeMvan den EsschertJWNioCYVerheijJReitsmaJBTerpstraVet al. Diagnostic Accuracy of MRI in Differentiating Hepatocellular Adenoma From Focal Nodular Hyperplasia: Prospective Study of the Additional Value of Gadoxetate Disodium. AJR Am J Roentgenol (2012) 199(1):26–34. doi: 10.2214/AJR.11.7750

  • 30

    AuerTAWalter-RittelTGeiselDSchningWFehrenbachU. HBP-Enhancing Hepatocellular Adenomas and How to Discriminate Them From FNH in Gd-EOB MRI. BMC Med Imaging (2021) 21(1):1–11. doi: 10.1186/s12880-021-00552-0

  • 31

    LeeJJeongWKLimHKKimAY. Focal Nodular Hyperplasia of the Liver: Contrast-Enhanced Ultrasonographic Features With Sonazoid. J Ultrasound Med (2018) 37(6):1473–80. doi: 10.1002/jum.14490

  • 32

    NguyenBNFléjouJFTerrisBBelghitiJDegottC. Focal Nodular Hyperplasia of the Liver: A Comprehensive Pathologic Study of 305 Lesions and Recognition of New Histologic Forms. Am J Surg Pathol (1999) 23(12):1441–54. doi: 10.1097/00000478-199912000-00001

  • 33

    FabreAAudetPVilgrainVNguyenBNVallaDBelghitiJet al. Histologic Scoring of Liver Biopsy in Focal Nodular Hyperplasia With Atypical Presentation. Hepatology (2002) 35(2):414–20. doi: 10.1053/jhep.2002.31103

  • 34

    RowanDJAllendeDSBellizziAMGillRMLiuXMcKenzieCAet al. Diagnostic Challenges of Focal Nodular Hyperplasia: Interobserver Variability, Accuracy, and the Utility of Glutamine Synthetase Immunohistochemistry. Histopathology (2021) 79(5):791–800. doi: 10.1111/his.14424

  • 35

    Bioulac-SagePLaumonierHRullierACubelGLaurentCZucman-RossiJet al. Over-Expression of Glutamine Synthetase in Focal Nodular Hyperplasia: A Novel Easy Diagnostic Tool in Surgical Pathology. Liver Int (2009) 29(3):459–65. doi: 10.1111/j.1478-3231.2008.01849.x

  • 36

    PerrakisADemirRMüllerVMulsowJAydinÜAlibekSet al. Management of the Focal Nodular Hyperplasia of the Liver: Evaluation of the Surgical Treatment Comparing With Observation Only. Am J Surg (2012) 204(5):689–96. doi: 10.1016/j.amjsurg.2012.02.006

Summary

Keywords

focal nodular hyperplasia (FNH), liver, rupture, acute abdomen, surgery

Citation

Si Y, Sun B, Zhao T, Xiao K, Zhao D-X and Huang Y-M (2022) Case Report: Rare Acute Abdomen: Focal Nodular Hyperplasia With Spontaneous Rupture. Front. Oncol. 12:873338. doi: 10.3389/fonc.2022.873338

Received

10 February 2022

Accepted

20 June 2022

Published

13 July 2022

Volume

12 - 2022

Edited by

Kun Zhang, Tongji University, China

Reviewed by

Alessio Vagliasindi, Santa Maria delle Croci Hospital, Italy; Jose M. Ramia, Hospital General Universitario de Alicante, Spain

Updates

Copyright

*Correspondence: Yong-Mao Huang,

This article was submitted to Surgical Oncology, a section of the journal Frontiers in Oncology

Disclaimer

All claims expressed in this article are solely those of the authors and do not necessarily represent those of their affiliated organizations, or those of the publisher, the editors and the reviewers. Any product that may be evaluated in this article or claim that may be made by its manufacturer is not guaranteed or endorsed by the publisher.

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