J Neurol Surg B Skull Base 2022; 83(01): 082-086
DOI: 10.1055/s-0040-1716692
Original Article

Management of Cutaneously Exposed Carotid Stents in Recurrent and Unresectable Head and Neck Cancer

1   Department of Neurological Surgery, Rush University Medical Center, Chicago, Illinois, United States
,
Ashley Heilingoetter
2   Department of Otolaryngology—Head and Neck Surgery, Ohio State University, Columbus, Ohio, United States
,
Christopher Rayle
3   Department of Otolaryngology—Head and Neck Surgery, University of Kentucky Medical Center, Lexington, Kentucky, United States
,
Thomas O'Toole
4   Department of Otolaryngology—Head and Neck Surgery, Spectrum Health Medical Group, Grand Rapids, Michigan, United States
,
Thomas J. Nielsen
5   Department of Otolaryngology—Head and Neck Surgery, Rush University Medical Center, Chicago, Illinois, United States
,
Richard Webster Crowley
1   Department of Neurological Surgery, Rush University Medical Center, Chicago, Illinois, United States
,
Samer Al-Khudari
5   Department of Otolaryngology—Head and Neck Surgery, Rush University Medical Center, Chicago, Illinois, United States
› Author Affiliations
Funding None.
 

Abstract

Objective Carotid blowout syndrome (CBS) is a rare but potentially life-threatening complication of head and neck cancer (HNC) treatment. Patients with CBS are managed with covered stents, limited published information exists regarding the management of delayed complications, specifically cutaneous exposure of stents. Here, we present our experience managing cutaneously exposed carotid artery stents (CAS) in patients with recurrent and unresectable HNC.

Methods A single-institution retrospective analysis was performed to identify recurrent HNC patients who underwent CAS placement for CBS and complicated with cutaneous exposure of the stent between 2014 and 2016. Medical records were reviewed with attention to treatment history, pre-, intra-, and postoperative courses, anticoagulation needs, and durability of the reconstruction.

Results We identified three patients who presented with a right CAS fully exposed in a large, ulcerative wound. All patients underwent a right pectoralis major myocutaneous flap (PMMF) to cover the exposed stent within 30 days of presentation to our institution. Two of three patients attained adequate coverage of the stent for more than 30 days, while one experienced partial flap dehiscence within 12 days. Two patients developed postoperative chest hematomas, which were managed conservatively. Two of three patients were able to undergo further palliative adjuvant treatments within 60 days of the initial surgical procedure.

Conclusion In this small series, durable coverage of an exposed carotid artery with PMMF was successful in two of three patients with extensive disease burden and complex prior treatment history. No mortalities occurred within 30 days postoperatively.


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Introduction

Head and neck cancer (HNC) is a major cause of morbidity and mortality in the United States with an estimated 61,000 new cases and 13,000 deaths annually.[1] Treatment options for HNC have evolved in recent decades, allowing for longer survival: the 5-year survival rate for oral cavity and pharyngeal cancers has increased from 52.7% in 1975 to 66.2% in 2008.[2] As survival from these cancers continues to improve, an increase in associated treatment- and disease-related complications is expected.

Carotid blowout syndrome (CBS), that is, rupture of the extracranial carotid arteries or their major branches, is one of the most feared complications, with a reported incidence of 3 to 4% in patients with HNC.[3] [4] [5] [6] [7] [8] [9] [10] CBS is associated with 60% morbidity and 40% mortality.[3] [4] [6] [7] [10] [11] [12] [13] In patients with advanced HNC, risk factors for the development of CBS are radiation, stripping of the carotid artery during surgery, skin breakdown, and development of mucocutaneous fistula.[14] CBS has historically been managed with surgical carotid artery ligation. However, more recently developed endovascular techniques, including selective embolization and reconstruction with covered stent grafts, have become the mainstay of treatment.[3] [4] [5] [6] [7] [8] [10] [11] [15]

Immediate complications associated with the use of covered stent grafts after CBS have been extensively reported and include acute thromboembolism and iatrogenic dissection. Mid- and long-term complications may involve rebleeding (13–44% incidence) and stent thrombosis associated or not symptomatic ischemic cerebrovascular accidents.[3] [5] [7] [8] [10] [13] [14] [15] [16] Nevertheless, the literature on cutaneous exposure of CAS and its management are scarce.[4] [17]

In this retrospective series, we describe our experience with recurrent unresectable HNC that underwent CAS placement for CBS treatment and complicated with cutaneous exposure of the stent. The use and rationale behind selecting the pectoralis major myocutaneous flaps (PMMF) for reconstruction in this particular cohort are discussed.


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Methods

A single-institution retrospective analysis was performed to identify recurrent HNC patients who underwent CAS placement for CBS and complicated with cutaneous exposure of the stent between 2014 and 2016. Medical records were reviewed with attention to cancer diagnosis, treatment history, pre-, intra-, and postoperative courses, anticoagulation needs, and durability of the reconstruction. The study was approved by the Rush University Medical Center Institutional Review Board.


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Results

We identified three male patients with diagnosis of head and neck squamous cell carcinoma, age ranged from 59 to 64 years, who presented with a right CAS exposed in a large, ulcerative wound. Treatment history for all patients involved at least one oncological surgery in addition to adjuvant chemotherapy and radiation.

Timing between CAS placement and cutaneous exposure ranged from 6 to 156 weeks. All patients underwent a right PMMF to cover the exposed stent within 30 days of presentation to our institution.

Reconstruction Technique

Initially the skin edges surrounding the wound of the exposed stent were debrided and freshened to allow for an inset of the planned flap. If the surrounding tissue can be cleared of gross malignancy, this was performed as in case 1 of our series. A myocutaneous pectoralis flap was harvested in the standard fashion centered on the pectoralis branch of the thoracoacromial artery. Sternal attachments and humerus attachments were released to allow for appropriate rotation and inset. Innervations to the pectoralis major muscle was transected during the harvest to allow for thinning of the flap. The skin paddle was fashioned to be inset to the surrounding tissue and the bulk of the pectoralis muscle overlying the stent and inset to the deeper tissue. The donor site was closed with local flaps in all cases and given the anticoagulated states of the patient's appropriate drains were used. ([Figs. 1]–[3])

Zoom Image
Fig. 1 Preoperative photo exhibiting the severity of the defect, with visible exposed mesh of the right carotid artery stent. This is Case 1.
Zoom Image
Fig. 2 Intraoperative photo demonstrating exposed carotid artery stent immediately prior to reconstruction with PMMF. PMMF, pectoralis major myocutaneous flap. This is Case 1.
Zoom Image
Fig. 3 Intraoperative photo taken prior to reconstruction with harvested PMMF, highlighting exposed right common carotid artery stent with visible mesh (white arrow). This is Case 2. PMMF, pectoralis major myocutaneous flap.

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Outcomes

Two of three patients attained adequate coverage of the stent for more than 30 days, while one experienced partial flap dehiscence within 12 days requiring surgical revision for wound debridement. Despite the flap dehiscence, the stent was still covered and the wound was managed conservatively with dressing changes and topical ointment. Two patients developed postoperative chest hematomas that were managed conservatively.

Two of three patients were able to undergo further palliative adjuvant treatments within 60 days of the initial surgical procedure. Wound healing time and, most significantly, the patient debilitating status were the reasons for adjuvant treatment delay.

Case 1 returned to work and upheld a reasonable quality of life within 3 weeks of surgery. Palliative treatment with immunotherapy was started 6 weeks after PMMF surgery due to problems with his port-a-cath. His follow-up in clinic was approximately 4 months after surgery showed adequate wound coverage ([Fig. 4]), and he eventually expired of regional and metastatic disease progression.

Zoom Image
Fig. 4 Postoperative photo demonstrating well-healed reconstruction approximately 4 months after surgery. This is Case 1.

Despite the partial flap dehiscence requiring debridement and wound care, case 3 was able to start palliative treatment with immunotherapy 3 weeks after PMMF surgery. He also underwent subsequent palliative systemic chemotherapy, palliative radiation to metastatic lung lesion and ultimately died in hospice care due to regional and metastatic disease progression 7.5 months after surgery.

The details on each case are summarized in [Table 1].

Table 1

Summary of cases with exposed CAS

Case no.

1

2

3

Age at presentation (y)/gender

59/male

64/male

61/male

1-degree cancer site

SCC of tongue

SCC: 1-degree site unknown

SCC of right tonsil

HPV status

Unknown

Unknown

Positive

Smoking status

Former smoker

Former smoker

Never smoker

Number of prior oncologic surgeries

2

1

2

Prior adjuvant treatments

Chemotherapy, radiation

Chemotherapy, immunotherapy, radiation

Chemotherapy, radiation

Prestent radiation dose

N/A

70 Gy to lesion; 60 Gy to bilateral neck

70 Gy to lesion; 30 Gy neck recurrence (×2)

Time from carotid stent placement to cutaneous exposure (wk)

16

6

152

Reconstruction method

PMMF

PMMF

PMMF

Excised skin margins positive for SCC?

No

Yes

Yes

Site of distant metastatic disease

Right neck

Right neck

Right neck, right lung

Postoperative anticoagulation

Aspirin, clopidogrel, enoxaparin (for PE)

Aspirin, clopidogrel

Aspirin, clopidogrel

Postoperative complications

Chest wall hematoma, cellulitis of neck with mild dehiscence

Mild flap dehiscence (stent remained covered)

Flap dehiscence, chest wall hematoma

Durable flap coverage[a]?

Yes

Yes

No, 12 days

Further postoperative adjuvant treatments?

Palliative with chemotherapy and immunotherapy

No

Palliative with chemotherapy, immunotherapy and palliative radiation to the lung

Abbreviations: CAS, carotid artery stents; HPV, human papillomavirus; N/A, not available; PE, pulmonary embolism; PMMF, pectoralis major myocutaneous flap; SCC, squamous cell carcinoma.


a Greater than 30 days of flap coverage is considered durable in this series.



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#

Discussion

Endovascular techniques designed to treat CBS have more recently come into favor, as they are less invasive than surgery and avoid the need to operate in a field often complicated by prior neck dissection and/or radiation therapy.[3] [9] [11] [12] Covered stent grafting is the preferred alternative in those who cannot tolerate occlusion of the offending carotid artery such as patients with contralateral carotid artery disease.[4] [5] [7] [12] [13] [14] [16]

Considering the potential catastrophic consequences of a hemispheric ischemic stroke, we believe all attempts should be made to preserve the internal carotid artery (ICA) and intracranial blood flow. Balloon test occlusions (BTO) may be challenging to perform in an emergency setting of a CBS. In addition, 15% of elective BTOs may have false negative results,[18] so ICA sacrifice should be used as a last resort to control bleeding.

In a CBS scenario, embolization or vessel sacrifice is a preferred treatment method when dealing with hemorrhage from external carotid artery or its branches. However, a reconstructive technique with stent is the preferred method when the bleeding source is the common or internal carotid arteries.

The most commonly reported mid- and long-term complications related to CAS in this patient population are rebleeding, infection, and stent thrombosis associated or not symptomatic ischemic cerebrovascular accidents. The complication of exposed CAS is an uncommonly reported in literature,[4] [17] and minimal published information exists regarding the management of such cases. As observed in our patient cohort, we believe this complication is likely associated with extensive history for the HNC treatment (multiple surgeries, radiation therapies, and chemotherapies), advanced disease, comorbidities, and poor nutritional status. We will likely see an increase in treatment- and disease-related complications as HNC survival continues to improve with better immunotherapies and chemotherapies.

Despite the widespread use of vascularized flaps to cover persistent soft tissue wounds in which the carotid artery is exposed,[4] [10] [13] there are no reports on the impact of having an exposed implant in these reconstructions. To the best of our knowledge, this is the first reported case series delineating the use of PMMF in this patient cohort.

Warren et al[4] published an excellent review and report of three patients with carotid blowout managed with endovascular stents and questioned the long-term safety of indwelling stents in the setting of head and neck malignancy. Although initial results in this article were favorable, two patients extruded their stent resulting in cerebrovascular accident in one case and thrombosis in the second.

Simental et al[17] reported two patients with poor outcomes with CAS exposure after treatment of CBS. The wound defect was covered with a total arm myocutaneous flap in the first case. The patient had new bleeding within 30 days after procedure requiring sacrifice of the common carotid artery, which resulted in an ischemic stroke and death. The second patient presented with CAS exposure after 8 weeks of placement. The common carotid artery had thrombosed and the patient subsequently expired to generalized inanition from recurrent carcinoma with no further bleeding.

Although microvascular surgery in vessel-depleted necks has been described in head and neck reconstruction, the extent of disease and severely debilitated and the anticoagulated state of this particular patient cohort persuaded us against free-tissue transfer. Our goal was to achieve an extremely low incidence of complete flap failure; as such, a pedicled flap was an ideal choice. The PMMF is particularly useful in salvage procedures, where the neck is vessel depleted, and also may allow for shorter operative times for wound coverage that is critical in this patient cohort. Often selected for its reliability, versatility, ease of harvest, and ability to cover large tissue defects in the head and neck region, the PMMF is easily mobilized and far reaching with the thoracoacromial artery as the axial vessel.[19] One distinct advantage of the short postoperative recovery period is the ability to undergo further systemic treatments after surgery, as seen in two patients in this series.

In the present series of salvage procedures, all patients faced posttreatment complications, including two patients who experienced postoperative bleeding and two with mild flap dehiscence. Patients with advanced HNC who have undergone numerous salvage treatments suffer treatment-related complications more readily, and rates of partial PMMF necrosis after salvage surgery tend to be higher than those undergoing primary surgery.[20] Therefore, discussion of the risks and benefits of palliative treatments is crucial.

In this case series, PMMF was used to cover exposed CAS and resulted in durable coverage in two of three cases. All patients experienced greater than 30 days of survival (range: 73–232 days) and were able to be discharged from the hospital after flap placement, and two of the three patients were able to undergo further palliative adjuvant therapies within 60 days of surgery. Although uncommon, cutaneously exposed intraluminal CAS present critical management considerations that are not yet well elucidated in the literature.


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Conclusion

Our experience suggests PMMF provide a durable, safe, and reliable option for coverage of exposed CAS, allowing patients to pursue further therapeutic or palliative treatments. Future comparative studies will aid in guiding the management of HNC patients with neck wounds containing exposed endovascular carotid artery stents.


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Conflict of Interest

None declared.

  • References

  • 1 Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin 2016; 66 (01) 7-30
  • 2 Howlader N, Noone A, Krapcho M. et al, eds. SEER cancer statistics review, 1975–2013, National Cancer Institute. Accessed April 26, 2016 at: http://seer.cancer.gov/csr/1975_2013/
  • 3 Gaba RC, West DL, Bui JT, Owens CA, Marden FA. Covered stent treatment of carotid blowout syndrome. Semin Intervent Radiol 2007; 24 (01) 47-52
  • 4 Warren FM, Cohen JI, Nesbit GM, Barnwell SL, Wax MK, Andersen PE. Management of carotid ‘blowout’ with endovascular stent grafts. Laryngoscope 2002; 112 (03) 428-433
  • 5 Powitzky R, Vasan N, Krempl G, Medina J. Carotid blowout in patients with head and neck cancer. Ann Otol Rhinol Laryngol 2010; 119 (07) 476-484
  • 6 Shah H, Gemmete JJ, Chaudhary N, Pandey AS, Ansari SA. Acute life-threatening hemorrhage in patients with head and neck cancer presenting with carotid blowout syndrome: follow-up results after initial hemostasis with covered-stent placement. AJNR Am J Neuroradiol 2011; 32 (04) 743-747
  • 7 McGettigan B, Parkes W, Gonsalves C, Eschelman D, Keane W, Boon MS. The use of a covered stent in carotid blowout syndrome. Ear Nose Throat J 2011; 90 (04) E17
  • 8 Chang FC, Luo CB, Lirng JF. et al. Evaluation of the outcomes of endovascular management for patients with head and neck cancers and associated carotid blowout syndrome of the external carotid artery. Clin Radiol 2013; 68 (11) e561-e569
  • 9 Gaynor BG, Haussen DC, Ambekar S, Peterson EC, Yavagal DR, Elhammady MS. Covered stents for the prevention and treatment of carotid blowout syndrome. Neurosurgery 2015; 77 (02) 164-167
  • 10 Liang NL, Guedes BD, Duvvuri U. et al. Outcomes of interventions for carotid blowout syndrome in patients with head and neck cancer. J Vasc Surg 2016; 63 (06) 1525-1530
  • 11 Chaloupka JC, Putman CM, Citardi MJ, Ross DA, Sasaki CT. Endovascular therapy for the carotid blowout syndrome in head and neck surgical patients: diagnostic and managerial considerations. AJNR Am J Neuroradiol 1996; 17 (05) 843-852
  • 12 Roh JL, Suh DC, Kim MR. et al. Endovascular management of carotid blowout syndrome in patients with head and neck cancers. Oral Oncol 2008; 44 (09) 844-850
  • 13 Farivar BS, Lee DH, Khalil A, Abrol S, Flores L. Carotid blowout syndrome: endovascular management of acute hemorrhage with tapering overlapped covered stents. Ann Vasc Surg 2014; 28 (08) 1934.e7-1934.e11
  • 14 Haas RA, Ahn SH. Interventional management of head and neck emergencies: carotid blowout. Semin Intervent Radiol 2013; 30 (03) 245-248
  • 15 Chang FC, Luo CB, Lirng JF. et al. Complications of carotid blowout syndrome in patients with head and neck cancers treated by covered stents. Interv Neuroradiol 2008; 14 (Suppl. 02) 29-33
  • 16 Pyun HW, Lee DH, Yoo HM. et al. Placement of covered stents for carotid blowout in patients with head and neck cancer: follow-up results after rescue treatments. AJNR Am J Neuroradiol 2007; 28 (08) 1594-1598
  • 17 Simental A, Johnson JT, Horowitz M. Delayed complications of endovascular stenting for carotid blowout. Am J Otolaryngol 2003; 24 (06) 417-419
  • 18 Chaudhary N, Gemmete JJ, Thompson BG, Pandey AS. Intracranial endovascular balloon test occlusion-indications, methods, and predictive value. Neurosurg Clin N Am 2009; 20 (03) 369-375
  • 19 Aničin A, Šifrer R, Strojan P. Pectoralis major myocutaneous flap in primary and salvage head and neck cancer surgery. J Oral Maxillofac Surg 2015; 73 (10) 2057-2064
  • 20 O'Neill JP, Shine N, Eadie PA, Beausang E, Timon C. Free tissue transfer versus pedicled flap reconstruction of head and neck malignancy defects. Ir J Med Sci 2010; 179 (03) 337-343

Address for correspondence

Samer Al-Khudari, MD
Department of Otorhinolaryngology—Head and Neck Surgery, Rush University Medical Center
1611 West Harrison Street, Suite 550, Chicago, IL 60612
United States   

Publication History

Received: 27 March 2020

Accepted: 25 July 2020

Article published online:
12 October 2020

© 2020. Thieme. All rights reserved.

Georg Thieme Verlag KG
Rüdigerstraße 14, 70469 Stuttgart, Germany

  • References

  • 1 Siegel RL, Miller KD, Jemal A. Cancer statistics, 2016. CA Cancer J Clin 2016; 66 (01) 7-30
  • 2 Howlader N, Noone A, Krapcho M. et al, eds. SEER cancer statistics review, 1975–2013, National Cancer Institute. Accessed April 26, 2016 at: http://seer.cancer.gov/csr/1975_2013/
  • 3 Gaba RC, West DL, Bui JT, Owens CA, Marden FA. Covered stent treatment of carotid blowout syndrome. Semin Intervent Radiol 2007; 24 (01) 47-52
  • 4 Warren FM, Cohen JI, Nesbit GM, Barnwell SL, Wax MK, Andersen PE. Management of carotid ‘blowout’ with endovascular stent grafts. Laryngoscope 2002; 112 (03) 428-433
  • 5 Powitzky R, Vasan N, Krempl G, Medina J. Carotid blowout in patients with head and neck cancer. Ann Otol Rhinol Laryngol 2010; 119 (07) 476-484
  • 6 Shah H, Gemmete JJ, Chaudhary N, Pandey AS, Ansari SA. Acute life-threatening hemorrhage in patients with head and neck cancer presenting with carotid blowout syndrome: follow-up results after initial hemostasis with covered-stent placement. AJNR Am J Neuroradiol 2011; 32 (04) 743-747
  • 7 McGettigan B, Parkes W, Gonsalves C, Eschelman D, Keane W, Boon MS. The use of a covered stent in carotid blowout syndrome. Ear Nose Throat J 2011; 90 (04) E17
  • 8 Chang FC, Luo CB, Lirng JF. et al. Evaluation of the outcomes of endovascular management for patients with head and neck cancers and associated carotid blowout syndrome of the external carotid artery. Clin Radiol 2013; 68 (11) e561-e569
  • 9 Gaynor BG, Haussen DC, Ambekar S, Peterson EC, Yavagal DR, Elhammady MS. Covered stents for the prevention and treatment of carotid blowout syndrome. Neurosurgery 2015; 77 (02) 164-167
  • 10 Liang NL, Guedes BD, Duvvuri U. et al. Outcomes of interventions for carotid blowout syndrome in patients with head and neck cancer. J Vasc Surg 2016; 63 (06) 1525-1530
  • 11 Chaloupka JC, Putman CM, Citardi MJ, Ross DA, Sasaki CT. Endovascular therapy for the carotid blowout syndrome in head and neck surgical patients: diagnostic and managerial considerations. AJNR Am J Neuroradiol 1996; 17 (05) 843-852
  • 12 Roh JL, Suh DC, Kim MR. et al. Endovascular management of carotid blowout syndrome in patients with head and neck cancers. Oral Oncol 2008; 44 (09) 844-850
  • 13 Farivar BS, Lee DH, Khalil A, Abrol S, Flores L. Carotid blowout syndrome: endovascular management of acute hemorrhage with tapering overlapped covered stents. Ann Vasc Surg 2014; 28 (08) 1934.e7-1934.e11
  • 14 Haas RA, Ahn SH. Interventional management of head and neck emergencies: carotid blowout. Semin Intervent Radiol 2013; 30 (03) 245-248
  • 15 Chang FC, Luo CB, Lirng JF. et al. Complications of carotid blowout syndrome in patients with head and neck cancers treated by covered stents. Interv Neuroradiol 2008; 14 (Suppl. 02) 29-33
  • 16 Pyun HW, Lee DH, Yoo HM. et al. Placement of covered stents for carotid blowout in patients with head and neck cancer: follow-up results after rescue treatments. AJNR Am J Neuroradiol 2007; 28 (08) 1594-1598
  • 17 Simental A, Johnson JT, Horowitz M. Delayed complications of endovascular stenting for carotid blowout. Am J Otolaryngol 2003; 24 (06) 417-419
  • 18 Chaudhary N, Gemmete JJ, Thompson BG, Pandey AS. Intracranial endovascular balloon test occlusion-indications, methods, and predictive value. Neurosurg Clin N Am 2009; 20 (03) 369-375
  • 19 Aničin A, Šifrer R, Strojan P. Pectoralis major myocutaneous flap in primary and salvage head and neck cancer surgery. J Oral Maxillofac Surg 2015; 73 (10) 2057-2064
  • 20 O'Neill JP, Shine N, Eadie PA, Beausang E, Timon C. Free tissue transfer versus pedicled flap reconstruction of head and neck malignancy defects. Ir J Med Sci 2010; 179 (03) 337-343

Zoom Image
Fig. 1 Preoperative photo exhibiting the severity of the defect, with visible exposed mesh of the right carotid artery stent. This is Case 1.
Zoom Image
Fig. 2 Intraoperative photo demonstrating exposed carotid artery stent immediately prior to reconstruction with PMMF. PMMF, pectoralis major myocutaneous flap. This is Case 1.
Zoom Image
Fig. 3 Intraoperative photo taken prior to reconstruction with harvested PMMF, highlighting exposed right common carotid artery stent with visible mesh (white arrow). This is Case 2. PMMF, pectoralis major myocutaneous flap.
Zoom Image
Fig. 4 Postoperative photo demonstrating well-healed reconstruction approximately 4 months after surgery. This is Case 1.