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31 Open Repair oftheSuperior Mesenteric Artery Aneurysm

Discussion

The most common type of superior mesenteric artery aneurysm is mycotic, secondary to bacte­rial endocarditis [1]. Atherosclerotic aneurysms in this location are rare. Superior mesenteric artery aneurysms though uncommon should be treated urgently to prevent rupture and ischemic and embolic complications [2]. Male patients and patients with very non-calcied aneurysms are at a greater risk of rupture [2].
Clinical diagnosis of a mesenteric arterial aneurysm is difcult, and the diagnosis is usually suggested by roentgenograms of the abdomen CT imaging selective arteriography in useful planning of endovascular or open repair. Of the 65 cases reported by DeBakey and Cooley, 63% were mycotic, 14% were syphilitic, and 23% were of unknown origin [1].
Operation is indicated for this condition, as one half of the superior mesenteric artery aneurysms, if left untreated, will spontaneously rupture [2]. In most cases, it is not necessary to restore arterial continuity after excision of aneurysm, since its slow occlusion with clot usually promotes the
development of an extensive collateral circulation [2]. However, the patient in this report had a partial celiac axis occlusion, and the pancreaticoduodenal collateral ow was reversed, resulting in a steal of blood from the mesenteric circulation. Since the bowel showed some discoloration, the jejunal artery was anastomosed to the side of the superior mesenteric artery after excision of the aneurysm. The small intestine regained its normal color. Endovascular repair with stent graft (balloon­expandable stent graft) has been described in high­risk patients [3].

References

1. Hans SS, Gordon M, Lee PT. Saccular atherosclerotic aneurysm of the superior mesenteric artery. Arch Surg. 1977;112:854.
2. Stone WM, Abbas M, Cherry KJ, Fowl RJ, Gloviczki P. Superior mesenteric artery aneurysms: is pres­ence an indication for intervention? J Vasc Surg. 2002;36:234–7.
3. Schweigert M, Adamus R, Stadhuber RJ, Stein HJ.Endovascular stent graft repair of a asymptomatic superior mesenteric artery aneurysm. Ann Vasc Surg. 2011;25:841e5–8.
Part IX
Resection of Carotid Body Tumor
Resection ofaMalignant Carotid Body Tumor withCarotid Artery Resection
32

Physical Examination

A 39-year-old male was presented to his family physician in 1999 with a mass in the right neck just below the angle of the mandible. The patient was referred to general surgery for possible cer­vical lymph node biopsy. During the biopsy, the general surgeon encountered excessive bleed­ing. He closed the incision and referred the patient to vascular surgery. CT scan of the neck showed a large vascular mass at the right carotid
Fig. 32.1 Carotid
arteriogram showing hypervascular carotid body tumor
bifurcation consistent with carotid body tumor. The patient’s main complaints were discomfort from the mass and episodes of coughing on turning the neck.

Procedure

He underwent selective carotid arteriography (Fig. 32.1) and embolization of the external carotid artery in preparation for its excision.
© Springer Nature Switzerland AG 2020 S. S. Hans, Challenging Arterial Reconstructions, https://doi.org/10.1007/978-3-030-44135-7_32
135
136
Fig. 32.2 Coil embolization of external carotid artery
32 Resection ofaMalignant Carotid Body Tumor withCarotid Artery Resection
External carotid artery was selectively cannu­lated along with its branches (Fig. 32.2). The coils were placed in the proximal maxillary artery, facial artery, and ascending pharyngeal and occipital artery to achieve complete external carotid artery occlusion. Gel-form particles were placed in the superior thyroid artery. In addition, PVA particles were also directed toward the vas­cular tissue. Under general anesthesia, the patient underwent excision of a large carotid body tumor via oblique neck incision. Dissection planes were difcult because of recent neck sur­gery. Common carotid artery was controlled in the inferior portion of the neck, and a silastic vessel loop was passed. External carotid artery was exposed and looped with vessel loop. Internal carotid artery was carefully mobilized
along with mobilization of the hypoglossal and vagus nerves. The hypoglossal nerve was looped with vessel loop. An attempt to separate the carotid body tumor from the adventitial plane of the carotid bifurcation was difcult, and it was decided to perform tumor resection along with resection of the distal common carotid and prox­imal internal carotid artery and ligation of the external carotid artery following systemic hepa­rinization. It is to be noted that two rubbery lymph nodes which measured 2.7 × 1.4cm were removed with the specimen. The specimen itself measured 3cm long bifurcated artery, 2cm seg­ment of external carotid artery, and 2.5 cm seg­ment of internal carotid artery. The excised mass measured 3 × 2.5 × 2cm.
After the resection of the mass, a non-reversed greater saphenous vein which was harvested from the groin and upper thigh was used as an interposition graft. Completion arteriogram showed satisfactory result. Final pathological diagnosis was metastatic paraganglioma into one lymph node. A section of the carotid body tumor showed histological features suggestive of para­ganglioma with nuclei which were moderately pleomorphic with increased mitosis. In addition, there was evidence of recent and old hemorrhage with foci of necrosis. The reticulin special stain showed distinct clustering of the neoplastic cells with variation in size of the cell nests.
The postoperative course was uneventful, except for the development of temporary hoarse­ness of the voice. He subsequently saw an ENT surgeon who diagnosed vocal cord weakness on the right side which improved over the ensuing 3 months. The patient was referred to medical oncology for further management of malignant carotid body tumor, and he received radiation therapy. However, the patient died 10 years later from widespread metastatic paraganglioma.

Discussion

Carotid body tumor is more prevalent in patients who are exposed to chronic hypoxemia including high altitudes, smoking, and chronic obstructive pulmonary disease. The majority of cases are
Discussion
137
sporadic; however approximately 10% occur along familial lines [15]. Carotid body tumors typically splay the carotid bifurcation and, depending on their size, can encapsulate the external or internal carotid artery or both. With carotid duplex imaging, a hypervascular mass with low ow resistance is demonstrated. Carotid arteriography, CTA, or MRA best denes the relationship of the tumor to the carotid bifurca­tion and location of the cranial nerves. The bulk of the tumor is generally located at and more often deep to the bifurcation and can extend over the common carotid artery proximally to the bifurcation. These tumors are slow growing with a reported median double time of 4.2years [5]. Carotid body tumors are usually extremely vas­cular and secrete catecholamines on rare occa­sions and are usually benign. When malignant (6–12.5%), carotid body tumors metastasize to local lymph nodes [2, 5]. Metastasis to the liver, lung, and bone does not occur in more than 5% of cases [2, 5].
Preoperative embolization of carotid body tumor is controversial [6]. Since these tumors are highly vascular, selective embolization of the ascending pharyngeal branch of the external carotid artery to reduce intraoperative bleeding is recommended. Many retrospective studies dem­onstrated no difference in blood loss or perioper­ative morbidity between embolized and non-embolized patients with carotid body tumors. Others have found reduced intraoperative bleeding after embolization of tumors of more than 3 cm diameter. Preoperative embolization procedure may result in stroke due to emboliza­tion of the particles into cerebral circulation. If preoperative embolization is decided, expedi­tious surgical resection should be performed preferably within 24 hours and no later than 48hours to avoid additional surgical difculties from inammatory reaction.
Injury to the cranial nerves, stroke, pseudoan­eurysm, and death are uncommon complications of carotid body tumors [15]. Baroreex failure is an uncommon but important complication fol­lowing bilateral carotid body tumor resection [5]. It should be suspected with the development of
tachycardia hypotension 24–72hours following resection of the tumor. Cranial nerve injury is the most common complication of carotid body tumor and may occur up to 24% in contemporary series. Most commonly injured cranial nerves include the vagus and hypoglossal nerve [5]. Deep retraction of the mandible may result in injury to marginal mandibular branch of the facial nerve [5].
Following exposure of the common carotid artery in the lower neck, the dissection should proceed cephalad. Early identication of the vagus nerve is important. Injuries to the cranial nerve increase with the size of the carotid body tumor and have been reported in up to 24% in contemporary series. The dissection plane is car­ried out in the subadventitial plane with the use of bipolar cautery. This avascular plane between the tumor and the media was described as the white line by Gordon-Taylor. Carotid body tumors’ blood supply is primarily from the exter­nal carotid artery, and therefore the use of throm­bin or regenerated cellulose helps in control of surface bleeding. If the patient did not undergo preoperative embolization of the external carotid artery, it should be ligated during the earlier part of the operation, thus decreasing overall bleeding and facilitate dissecting the tumor from the inter­nal carotid artery.
An internal to external carotid dissection technique has also been described. This is per­formed by beginning the dissection from the white line on the common carotid artery and then dissecting the tumor free of the internal carotid artery with dissecting scissors. The external carotid artery is the last artery to be dis­sected. The advantage of this technique includes shorter dissection time. Some authors have advocated a cranial to caudal method of carotid body tumor resection. This approach is based on the course of ascending pharyngeal artery which is considered to be a major source of blood sup­ply to the tumor. Each approach has its own advantage and disadvantages, and it is up to the individual surgeon to know their skill set and choose the approach which is most likely to decrease the morbidity.
138
32 Resection ofaMalignant Carotid Body Tumor withCarotid Artery Resection

References

1. Pacheco-Ojeda LA. Carotid body tumor: surgical experience in 215 cases. Jr Cranio- Maxillo– Facial Surg. 2017;45:1472–7.
2. Hinojosa CA, Ortiz-Lopez LJ, Anaya–Ayalo JE, Orozco–Sevilla V, et al. Comparison of retrocarotid and caudocranial dissection technique for the surgi­cal treatment of carotid body tumors. J Vasc Surg. 2015;62:958–64.
3. Davila VJ, Chang JM, Stone WM, Ford RJ, et al. Current surgical management of carotid body tumors. J Vasc Surg. 2016;64:1703–10.
4. Kim GY, Lawrence PF, Moridzadeh RS, Zimmerman K, etal. New predictors of complica­tions in carotid body tumor resection. J Vasc Surg. 2017;65:1673–9.
5. Davis FM, Obi A, Osborne N.Carotid body tumors. In: Hans SS, editor. Extracranial carotid and ver­tebral artery disease. Cham: Springer; 2018. p.253–60.
6. Power AH, Bover TC, Kasperbauer J, Link MJ, et al. Impact of pre-operative embolization on outcomes of carotid body resection. J Vasc Surg. 2012;56:979–89.
Resection ofaLarge Carotid Body Tumor withMandibular Subluxation
History andPhysical Examination
A 52-year-old male with history of hyperten­sion came to the emergency room with vague neurological symptoms. A CTA of the head and neck was obtained which showed a large right carotid body tumor. The upper extent of the tumor was of the junction of C1 and C2 verte­bral body (Fig. 33.1). The patient also under­went catheter- based carotid and cerebral angiography which showed a very large vascu­lar carotid body tumor extending toward the base of the skull. The tumor was 5.3 cm in length and 4.8cm in transverse diameter. As the tumor was large and was extending toward the base of the skull, it was decided to perform mandibular subluxation.

Procedure

Under nasotracheal intubation, mandibular sub­luxation was performed by a maxillofacial sur­geon. EEG monitoring and SSEP (somatosensory evoked potentials) were performed as well. A slightly curved hockey stick incision was made behind the lobule of the ear extending along the anterior border of the sternomastoid. In the infe­rior portion of the neck, the carotid sheath was opened, silastic vessel loop was passed to the common carotid artery, and the vagus nerve was
33
Fig. 33.1 Large carotid body tumor
preserved. In the cephalad portion of the dissec­tion, the posterior belly of the digastric muscle was exposed, and the hypoglossal nerve could be seen coursing over the large carotid body tumor (Fig. 33.2). The hypoglossal nerve was looped with a silastic loop.
The dissection was started at the carotid
bifurcation, and the branches of the external carotid artery were carefully exposed and ligated. Bipolar cautery was used. Silastic loop doubled on itself was passed around the external carotid artery. Initial dissection was started behind the external carotid artery to expose the medial wall of the tumor. The tumor was care­fully separated from the pharyngeal wall. The tumor was then mobilized beneath the hypo­glossal nerve, and all the feeding branches were carefully controlled by silk ties. Dissection was done along the lateral wall of the carotid artery. There was a small amount of bleeding from the internal carotid artery and arterial wall which
© Springer Nature Switzerland AG 2020 S. S. Hans, Challenging Arterial Reconstructions, https://doi.org/10.1007/978-3-030-44135-7_33
139
140
Fig. 33.2 CTA showing extent of large carotid body tumor
33 Resection ofaLarge Carotid Body Tumor withMandibular Subluxation
was controlled with a transversely placed suture of 7-0 cardiovascular Prolene. The internal carotid artery diameter was slightly smaller than average, possibly from compression due to a large carotid body tumor. As the dissection was proceeding, there were ischemic changes in the EEG, and one could not palpate the pulse in the internal carotid artery. The patient was given 10,000units of heparin by the anesthesia. The common carotid artery was controlled, and an incision was made in the internal carotid artery extending to the common carotid artery, and a grayish-white platelet thrombus was removed with brisk backbleeding from the internal carotid artery.
At this stage, a Sundt shunt (3 × 4mm) was inserted with the smaller end into the internal carotid artery followed by larger end into the common carotid artery. The ow from the shunt was conrmed with Doppler probe. A bovine pericardial patch was sutured to the internal carotid artery and to the common carotid artery. A completion arteriography was performed through the branches of the external carotid artery with a catheter to the common carotid artery which showed satisfactory lling of the
anterior cerebral artery and superior branch of the middle cerebral artery but poor lling of the branches of inferior branches of the middle cere­bral artery (Fig.33.3). There was some irregular­ity at the site of the patch grafting, but no denite stenosis could be seen on the completion arterio­gram (Fig. 33.4). The remaining tumor was removed, and in the recovery room, the patient was found to have weakness of the left upper extremity. He required ventilatory support and was seen by an interventional neurosurgeon, but it was decided since the occlusion was in the dis­tal branches of the middle cerebral artery (infe­rior branch) that mechanical retrieval of emboli was not to be recommended. The patient under­went non-contrast MRI brain which showed in fact in the distribution of the inferior branch of the middle cerebral artery. The patient developed deep venous thrombosis of the right lower extremity and had inferior vena cava lter place­ment because anticoagulation was thought to be contraindicated.
The patient remained on ventilatory support with a nasogastric tube. The patient subse­quently underwent tracheostomy and PEG tube placement. He continued to improve over the

Discussion

141
Fig. 33.3 Carotid arteriography showing hypervascular carotid body tumor
next 3 months. He was ambulating; however he had weakness of the left upper extremity (grade
stockings. Patient’s compliance for his medical care has been poor.
3/5). His main difculty was pain and dimin­ished range of movement in the left shoulder from lack of use although he was receiving
Discussion
physical and occupational therapy. The patient was non- compliant. The patient continued to make improvement and was subsequently dis­charged home from an extended care facility
This tumor represented Shamblin type II tumor. Shamblin classication of carotid body tumors includes:
after 3 months of stay.
The patient was admitted to a correctional facility on account of illegal drug possession charge. The patient was last seen in January 2020 with minimal weakness of the left upper extrem­ity. Attempted retrieval of an IVC lter was unsuccessful on Jan 13, 2020, as IV cavagram showed chronically occluded IVC. The patient had minimal swelling of both lower extremities and was recommended to wear compression
• Type I – tumors are small in location of the carotid bifurcation and can be removed with­out difculty.
• Type II – tumors are large, splay the carotid bifurcation, but do not circumferentially encase the carotid arteries.
• Type III – tumors are large and encapsulate the internal and external carotid arteries and often adhere to adjacent cranial nerves.
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33 Resection ofaLarge Carotid Body Tumor withMandibular Subluxation
In this patient, the extent of the dissection
(caudal to cranial) and the extent of the large carotid body tumor probably lead to kinking of the internal carotid artery during manipulation and thrombosis which was diagnosed by EEG monitoring. Risk factors for stroke during removal of carotid body tumor include excessive manipulation of tumor with possible kinking or stenosis from the repair of the internal carotid artery. Full-dose heparinization prior to manipu­lation of the internal carotid artery, a traumatic vascular clamp, and shrink is required (based on low stump pressure or EEG/SSEPs changes). In a recent analysis of 500 contemporary cases, intra­and postoperative stroke following carotid body tumor occurred in about 4% of cases. Mortality has been reported to be around 1% (30-day mor­tality) [1].

Reference

Fig. 33.4 Operative carotid arteriogram showing irregu-
larity at the site of carotid patch and absent lling of the inferior branches of the middle cerebral artery with absent ow in the external carotid artery
1. Davis FM, Obi A, Osborne N. Carotid body tumors. In: Hans SS, editor. Extracranial carotid and verte­bral disease – contemporary management. Cham: Springer; 2018. p.253–60.