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CVIR Endovascular

, 1:34 | Cite as

Bladder wall and surrounding tissue necrosis following bilateral superselective embolization of internal iliac artery branches due to uncontrollable haematuria related to bladder tumor: case report

  • Andrey Tarkhanov
  • Gabriel Bartal
  • Sergey Druzhin
  • Rafael Shakhbazyan
  • Evgenii Grebenev
  • Maxim Kartashov
Open Access
Case Report
  • 47 Downloads

Abstract

Background

Case of urinary bladder wall and surrounding tissue necrosis following bilateral superselective embolization of internal iliac artery branches due to unmanageable haematuria associated with aggressive bladder tumor.

Case

We achieved the bleeding control, but patient demonstrated severe postembolization syndrome at follow-up (low abdominal pain, arterial hypertension, hyperthermia). Severe bladder tissue and surrounding neoplastic tissue necrosis developed several days after procedure. Patient died from multiple organ dysfunction syndrome due to longstanding peritonitis.

Conclusions

Tumor ischemia and bladder wall and surrounding tissue necrosis, are possible serious complications ofembolization using calibrated microspheres. These complications can be very dangerous, and even fatal.

Keywords

Bladder tumor embolization Lower urinary tract bleeding Bladder malignancies Embolization particles 

Abbreviations

CT-Angiography

Computedtomographyangiography

HGB

Hemoglobin

IR

interventional radiology

IV

intravenous

MRI

Magneticresonanceimaging

NSAIDs

Nonsteroidal anti-inflammatorydrugs

PVA

Polyvinyl alcohol

Background

Embolization of bleeding due to locally advanced bladder tumors is one of the most effective and minimally invasive methods, especially in cases of non-operative bleeding that doesn‘t react to conservative treatment. Severe complications are rare, but if they occur, patient’s well-being would be at risk (Korkmaz et al., 2016; Greenstein et al., 1983). Complications can manifest as fever, pelvic pain, nausea (all of this is associated with postembolization syndrome and can be managed with NSAIDs). Minor complications can occur on first postprocedural days. It can be infection, urinary incontinence, retention of urine, prostatitis, soft tissue and penile ischemia (Greenstein et al., 1983). All of the conditions should be managed conservatively.Recently several case reports with positive outcome have been published (Vikash Prasad, 2009; Korkmaz et al., 2016; Pereira et al., 2000; Pereira & Phan, 2004; Carmignani et al., 1980; El-Assmy & Mohsen, 2007). In this communication we describe case of tumor and surrounding bladder tissue necrosis following bladder arteries embolization due to macrohaematuria.

Case presentation

A 58-year-old male arrived at policlinic. He complained on dysuria, ischuria for several months and macrohaematuria. He did not have physical symptoms of acute blood loss. Serum Creatinine level was normal (68 mg/dL). Ultrasound examination of kidneys and urinary tract revealed solid bladder mass of about 55 mm in diameter without signs of metastatic spread. Patient had no significant anemia (HGB 117 g/l), but HGB level decreased from 143 g/l in two days.

Before hospitalization additional imaging was performed:
  • MRI: bladder tumor 63 mm with invasion of the right ureter with right ureterohydronephrosis.

  • On nephroscintigraphy: nonfunctioning right kidney.

  • Irrigation through the three-way catheter was ineffective.

  • Conservative treatment of haematuria (Транексам® (Tranexam), Obninsk, Russian Federation, tablets 500 mg 3 times per day) was ineffective.

  • Cystoscopy was non-informative due to profuse haematuria, with multiple blood clots in the bladder.

After following discussion with referring physician it was decided to perform selective embolization of bladder tumor due to potential life-threatening blood loss. Pre-operative CT-Angiography showed significant neovasculaturization of the tumor without obvious source of active bleeding.

Patient underwent an embolization procedure: Right Common Femoral artery access (Vascular sheath Prelude 5F, Merit Medical, USA., catheter Cobra C2 5F, Merit Medical, U.S.A.), bilateral superselective embolization of anterior division branches of Internal Iliac Arteries using microcatheter 2,4F (Progreat-α micro catheter, Terumo Corporation, Japan) and Avigo hydrophilic guidewire, Medtronic, USA). Superior and inferiorvesical arteries on both sides (Figs. 1 and 2), left prostatic artery and left obturator arteries were embolized using 500 μm Embozene particles (Boston Scientific Corporation, USA) 1 vial per procedure (diluted with contrast media and saline in amount to stable suspension) to achieve subtotal stasis (near absence of contrast enhancement of distal parts of above-mentioned arteries), subtotal embolization of both anterior portions of Internal Iliac Arteries (notable ceasing of contrast flow from arising point) upon exit using gelfoam (Pfizer, USA) and Embozene suspension (self-made combination of Gelfoam particles about 20% of 10 ml syringe volume, mixed with Embozene spheres about 10% of syringe volume with contrast media and saline) (Figs. 3 and 4). Such comprehensive embolization was performed as our dedicated medical facility with determined equipment is exclusive in terms of treating oncology patients and this particular patient can’t be brought here in time if bleeding reoccure at home.
Fig. 1

Neovascularization in projection of tumor bed

Fig. 2

Finishing embolization on the left side

Fig. 3

Finishing embolization on the right side

Fig. 4

Right side after finishing the procedure

The procedures were performed under local anesthesia using Lidocain 1%. Intravenous Fentanyl 0,2 mg (Fentanyl, Moscow endocrine factory, Moscow, Russia) was injected before embolization for analgesia during the procedure and programmed IV morphine pump connected following the procedure. Patient suffered from severe pelvic pain for 4 h after the procedure and mild pain in pelvic area for 2 days. Haematuria ceased on day 3 after the procedure. For planning further treatment transurethral biopsy of the mass was performed, necrotic villous papillary tumor in lower semicircle of the bladder was visualized. Two days later urologist diagnosed peritonitis. On Ultrasound examination massive amount of free hyperechoic liquid, without gas was reported. Urgent exploratory laparotomy shown 3 to 4 l of free muddy smelly fluid in the abdominal cavity and total necrosis of the bladder wall. Sanation of abdominal cavity, necrectomy, cystostomy, and bilateral nephrostomy were performed. Patient deceased from multiple organ failure on day eight despite symptomatic therapy in intensive care unit. An autopsy report described total necrosis of tumor with necrosis of underlying bladder wall and multiple organ failure due to sepsis (Figs. 5 and 6).
Fig. 5

Totally necrotized tumor and underlying bladder wall

Fig. 6

Microscopic view (normal muscle tissue, demarcation zone, tumor tissue and microembolus in vessel)

Conclusion

Chronic bleeding has been described in cases of most significant problems of oncourology. Oncologic patient can face a permanent cascade of disbalance between pathways of coagulation (Fricke et al., 2017; Salignac et al., 2002; Kennedy et al., 2016; Zhu et al., 2016). These patientsare in slightly greater risk of bleeding without any surgical procedure and greater risk of bleeding in post-operative period. The most common cause of such complication could be a diffuse bleeding from traumatized tumor tissue surface after cystoscopic punch-biopsy. Conservative methods of bleeding control (Kolev & Longstaff, 2016) (fibrinolysis inhibitors) will be ineffective in most cases. It’s a complex situation, because not each all patient from this cohort can survive cystostomy due to poor performance status. Recently, superselective embolization became the method of choice to control such bleeding. Besides, physicians choose embolization among other methods of treatment for acute bleeding: combined trauma with pelvic fractures, uncontrollable bleedings after gynecological surgical operations and complications of radiotherapy (may be chronic as well) (Agolini et al., 1997; Matityahu et al., 2013; Ali et al., 2014; Sieber, 1994; Samuel Washington & Benjamin, 2016; El-Shalakany, 2003). Usually, sequence of actions comprises bilateral diagnostic angiography of internal iliac arteries in order to determine a source of bleeding (arterial supply of bladder tumors can originate from superior and/or inferior vesical arteries, prostatic arteries, not infrequently it may be branches of internal pudendal artery, obturator arteries (Vikash Prasad, 2009)) followed by superselective embolization using various embolic agents. The most frequently-used agents are embolic spheres of different sizes, that can provide permanent tumor vessels occlusion (choosing spheres diameter depends on expected vessel penetration), but IRs also can use polymorphic PVA agents (also permanent occlusion), gelfoam particles (temporary occlusion) or combinations of those. Described method are effective alternative to surgery. Embolization can be performed even in the in patients in shock and with high procedure success. The patient does not require special preparations. Despite obvious advantages and minimally invasive character of the procedure, in some cases embolization can lead to serious complications. In retrospective study of Matityahu et al. (Matityahu et al., 2013) authors report 11% chance of complications, including one case of bladder necrosis from cohort of 98 patients. Serious complications were reported in all patients who underwent bilateral embolization. A major complication as bladder necrosis is described within the first 4–5 weeks following the embolization (Ali et al., 2014; Sieber, 1994), however, we have found data of bladder necrosis in earlier post-operative period (two weeks after intervention) (Sieber, 1994; Samuel Washington & Benjamin, 2016).

In our previous experience with over 40 embolizations of bleeding Bladder tumors we used spherical calibrated BeadBlock (BTG) and EmboGold by Merit Medical particles we did not observe such complications with similar aggressive character of performed procedures.

In our patient bladder necrosis occurred within 10 postembolization days. Factors that may contribute in developing of such life-threatening condition: tissue hypoperfusion and potential non-target embolization of non-involved in tumor supply bladder arteries, lack of good collateral flow due to patient abnormality such as atherosclerosis, hypovolemia due to developed sepsis. We associate this phenomenon with use of strictly-calibrated microspheres with high concentration of particles per unit of volume (in comparison of non-strictly calibrated PVA particles or gelfoam). Strictly calibrated embolic agent is expected to have greater ability to penetrate the arteries with an exceptional dense filling capabilities, which can despite relatively large size of each sphere (500 μm) lead to complete tumor and some bladder wall ischemia.It seems that strictly-calibrated microspheres do provide a desired haemostatic effect, but we have to carefully chooseappropriate size of embolic agent according with vessel size of the target organ.

Methods of embolization for bleeding control are firmly established in daily practice. Indisputable advantages of embolization therapy provide an opportunity to use it for patients with poor performance status, who can’t survive surgery or have contraindications for general anesthesia. Yet, even minimally-invasive treatment with overly aggressive approach can lead to life-threatening conditions. Such potential complication has to be discussed with the patient prior to the procedure and signing the informed consent. Each individual case requires a correct estimate of tumor blood supply and collateral flow followed by subtotal embolization of vessels feeding the tumor. Based on described method of bladder tumor embolization using strictly-calibrated microspheres (EmboZene) we recommend to avoid use of particles sized 500μmor less, as it can lead to total necrosis of the tumor and surrounding bladder tissue. In situations with less accessibility of catlabs for population from very remote locations, the goal is to find balance between significantly diminish the flow in tumor vessels to achieve stable hemostasis within the limits of single procedure, but not complete cease of blood flow in the tumor bed in case of compromised collateral flow.

Notes

Acknowledgements

Not applicable

Funding

Approved waivers request.

Availability of data and materials

Data sharing not applicable to this article as no datasets were generated or analysed during the current study.

Authors’ contributions

AT carried out endovascular surgery, drainage; created case design, drafted the manuscript, participated in coordination. GB participated in creation of case design, drafted the manuscript.SD carried out endovascular surgery, drainage; created case design, drafted the manuscript.RS carried out endovascular surgery, drainage; created case design, drafted the manuscript.EG performed digital imaging and image analysis.MK performed digital imaging and image analysis. All authors read and approved the final manuscript.

Ethics approval and consent to participate

Not applicable. This case report don’t need ethic approval. Personal consent for using anonymous personal data for science purpose had been received at pre-operative stage.

Consent for publication

Case report does not contain individual personal data of any kind.

Competing interests

The authors declare that they have no competing interests.

Publisher’s Note

Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

References

  1. Agolini SF, Shah K, Jaffe J, Newcomb J, Rhodes M, Reed JF III (1997) Arterial embolization is a rapid and effective technique for controlling pelvic fracture hemorrhage. The Journal of Trauma: Injury, Infection and Critical Care 43(3):395–399.  https://doi.org/10.1097/00005373-199709000-00001 CrossRefGoogle Scholar
  2. Ali A, Nabi G, Swami S, Somani B (2014) Bladder necrosis secondary to internal iliac artery embolization following pelvic fracture. Urology Annals 6(2):166–168.  https://doi.org/10.4103/0974-7796.130657 CrossRefPubMedPubMedCentralGoogle Scholar
  3. Carmignani G, Belgrano E, Puppo P, Cichero A, Giuliani L (1980) Trans-catheter embolization of the hypogastric arteries in cases ofbladder hemorrhage from advanced pelvic cancers: follow-upin 9 cases. J Urol 124:196–200CrossRefPubMedGoogle Scholar
  4. El-Assmy A, Mohsen T (2007) Internal iliac artery embolization for thecontrol of severe bladder hemorrhage secondary to carcinoma:long-term follow-up. Sci World J 17:1567–1574CrossRefGoogle Scholar
  5. El-Shalakany AH1, Nasr El-Din MH, Wafa GA, Azzam ME, El-Dorry A (2003) Massive vault necrosis with bladder fistula after uterine artery embolisation. First published: February 2003 DOI:  https://doi.org/10.1046/j.1471-0528.2003.01151.x
  6. Fricke A, Ullrich PV, Cimniak AFV, Becherer C, Follo M, Heinz J, Scholber J, Herget GW, Hauschild O, Wittel UA, Stark GB, Bannasch H, Braig D, Eisenhardt SU (2017) Levels of activated platelet-derived microvesicles in patients with soft tissue sarcoma correlate with an increased risk of venous thromboembolism. BMC Cancer 17(1):527.  https://doi.org/10.1186/s12885-017-3515-y. CrossRefPubMedPubMedCentralGoogle Scholar
  7. Greenstein A, Merimsky E, Papo J, Braf Z. Persistent glutealpain after embolization of the hypogastric arteries. An unexpected complication. J Urol. 1983;89:595–596Google Scholar
  8. Kennedy AR, Maity A, Sanzari JK. A Review of radiation-induced coagulopathy and new findings to support potential prevention strategies and treatments. Radiat Res 2016186(2):121–140. doi:  https://doi.org/10.1667/RR14406.1. Epub 2016 Jul 26
  9. Kolev K, Longstaff C (2016) Bleeding related to disturbed fibrinolysis. Br J Haematol 175(1):12–23.  https://doi.org/10.1111/bjh.14255 Epub 2016 Aug 1CrossRefPubMedPubMedCentralGoogle Scholar
  10. Korkmaz M, Şanal B, Aras B, Bozkaya H, Çınar C, Güneyli S, Gök M, Adam G, Düzgün F, Oran I. The short- and long-term effectiveness of transcatheter arterial embolization in patients with intractable hematuria. Diagn Interv Imaging. 2016 Feb;97(2):197–201. doi:  https://doi.org/10.1016/j.diii.2015.06.020. Epub 2015 Oct 23. DOI: https://doi.org/10.1016/j.diii.2015.06.020
  11. Matityahu A, Marmor M, Elson JK et al (2013) Acute complications of patients with pelvic fractures after pelvic angiographic embolization. Clin Orthop Relat Res 471(9):2906–2911.  https://doi.org/10.1007/s11999-013-3119-z CrossRefPubMedPubMedCentralGoogle Scholar
  12. Pereira J, Mancini I, Bruera E (2000) The management of bleedingin patients with advanced cancer. In: Portenoy RK, BrueraE,editors. Topics in palliative care, Vol. 4. New York: Oxford University Press; p. 163–83Google Scholar
  13. Pereira J, Phan T (2004) Management of bleeding in patients withadvanced cancer. Oncologist 9:561–570CrossRefPubMedGoogle Scholar
  14. Salignac S, Walter A, Feugier P, Lecompte T, Lesesve JF (2002) Solid tumor in terminal phase: interpretation of biologic anomalies (hematologic tests). Ann BiolClin (Paris) 60(1):96–100Google Scholar
  15. Samuel Washington, E. Charles Osterberg, [...], and Benjamin N (2016) Breyer Acute Bladder Necrosis after Pelvic Arterial Embolization for Pelvic Trauma: Lessons Learned fromTwo Cases of Immediate Postembolization Bladder Necrosis. Case Rep Urol. 2016: 7594192. Published online 2016 Sep 5Google Scholar
  16. Sieber PR (1994) Bladder necrosis secondary to pelvic artery embolization: case report and literature review. J Urol 151:422CrossRefPubMedGoogle Scholar
  17. Prasad V, Sacks BA, Kraus S, Clouse ME (2009) Embolotherapy for Lower Urinary Tract Hemorrhage. DOI:  https://doi.org/10.1016/j.jvir.2009.04.048
  18. Zhu YW, Feng TB, Zhou XJ, Hu XL, Ding J, Zhu WY, Qian DP, Sun YW (2016) Routine hemostasis and Hemogram parameters: valuable assessments for coagulation disorder and chemotherapy in Cancer patients. Chin Med J 129(15):1772–1777.  https://doi.org/10.4103/0366-6999.186637

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© The Author(s) 2018

Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.

Authors and Affiliations

  1. 1.Sverdlovsk Regional Oncology Center - Interventional RadiologyYekaterinburgRussia
  2. 2.Meir MC (Medical Center), RadiologyKfar-SabaIsrael

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