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Case Report Spontaneous Isolated Visceral Artery Dissection in a Middle Aged Male Eric Melnychuk and Robert Strony Department of Emergency Medicine, Geisinger Medical Center, 100 North Academy Avenue, Danville, PA 17822, USA Correspondence should be addressed to Eric Melnychuk; [email protected] Received 12 September 2016; Accepted 4 December 2016; Published 1 January 2017 Academic Editor: Aristomenis K. Exadaktylos Copyright © 2017 E. Melnychuk and R. Strony. is is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Epigastric pain is a common complaint made by patients being evaluated in the emergency department. Spontaneous isolated visceral artery dissection is a rare cause with no reported prevalence. We present a case of a 37-year-old male evaluated in the emergency department for epigastric pain and subsequently diagnosed with a spontaneous isolated celiac artery dissection with involvement of the hepatic and splenic arteries. Recent case series suggest this disease may be managed medically in most cases. Surgical intervention may be considered for significant bleeding or signs of intestinal ischemia. 1. Case Report A 37-year-old Caucasian male presented to an emergency department with worsening epigastric pain of 4-day duration. He stated that his pain initially began as indigestion while he was leaning forward getting out of bed and progressed to a constant aching pain with associated nausea. He stated that bending forward exacerbated the pain. He denied prandial pain, melena, hematochezia, or recent change in bowel habits. History was notable for hypertension which was being managed without need for antihypertensive medications. Surgical history was not significant for any prior abdominal surgeries. His social history was significant for tobacco abuse which consisted of a half pack of cigarettes a day for 25 years. Initial vital signs were significant for hypertension. Physical exam on presentation was significant for minimal epigastric tenderness with normoactive bowel sounds without rebound or guarding. Lab analysis was not significant for elevated lipase, liver function abnormalities, anemia, or electrolyte abnormalities. Computed tomography (CT) of the abdomen and pelvis with IV contrast was performed which showed a filling defect in the celiac artery. Due to concern for dissection, a CT angiogram of the abdomen and pelvis was performed. e CT angiogram showed a 40.1 mm dissection from the celiac origin into the hepatic artery as well as a 37.9mm dissection from the celiac origin into the splenic artery (Figures 1 and 2). He was also found to have a beaded-appearing leſt main renal artery, raising concerns for fibromuscular dysplasia. e patient was admitted for observation, given 1000 mL unfractionated heparin bolus, and started on an unfraction- ated heparin infusion. e patient was evaluated by vascular surgeons and gastroenterologists. When given the choice for stenting the lesion for symptomatic control, he elected not to have the lesion stented. Prior to discharge he was started on 81 mg aspirin daily and a follow-up appointment with repeat CT angiography was scheduled in 2 months. Follow- up CT angiogram two months aſter his initial diagnosis showed minimal enlargement of the dissection. At that time during his vascular surgery follow-up, the patient stated improvement in his abdominal pain. At that time he was scheduled for a 6-month appointment and follow-up CTA. 2. Discussion Visceral artery dissection typically occurs as a complication of an extension of a descending aortic dissection. However, spontaneous isolated visceral artery dissection has been described in the literature. e prevalence and etiology of this disease are unknown as it is uncommon and the literature consists only of case reports and case series. Spontaneous dissection of the superior mesenteric artery is most common, Hindawi Case Reports in Emergency Medicine Volume 2017, Article ID 3704348, 3 pages https://doi.org/10.1155/2017/3704348

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Page 1: Spontaneous Isolated Visceral Artery Dissection in a ... · CaseReport Spontaneous Isolated Visceral Artery Dissection in a Middle Aged Male EricMelnychukandRobertStrony DepartmentofEmergencyMedicine,GeisingerMedicalCenter,100NorthAcademyAvenue,Danville,PA17822,USA

Case ReportSpontaneous Isolated Visceral Artery Dissection ina Middle Aged Male

Eric Melnychuk and Robert Strony

Department of Emergency Medicine, Geisinger Medical Center, 100 North Academy Avenue, Danville, PA 17822, USA

Correspondence should be addressed to Eric Melnychuk; [email protected]

Received 12 September 2016; Accepted 4 December 2016; Published 1 January 2017

Academic Editor: Aristomenis K. Exadaktylos

Copyright © 2017 E. Melnychuk and R. Strony. This is an open access article distributed under the Creative Commons AttributionLicense, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properlycited.

Epigastric pain is a common complaint made by patients being evaluated in the emergency department. Spontaneous isolatedvisceral artery dissection is a rare cause with no reported prevalence. We present a case of a 37-year-old male evaluated in theemergency department for epigastric pain and subsequently diagnosed with a spontaneous isolated celiac artery dissection withinvolvement of the hepatic and splenic arteries. Recent case series suggest this disease may be managed medically in most cases.Surgical intervention may be considered for significant bleeding or signs of intestinal ischemia.

1. Case Report

A 37-year-old Caucasian male presented to an emergencydepartmentwithworsening epigastric pain of 4-day duration.He stated that his pain initially began as indigestion while hewas leaning forward getting out of bed and progressed to aconstant aching pain with associated nausea. He stated thatbending forward exacerbated the pain. He denied prandialpain, melena, hematochezia, or recent change in bowelhabits. History was notable for hypertension which was beingmanaged without need for antihypertensive medications.Surgical history was not significant for any prior abdominalsurgeries. His social history was significant for tobacco abusewhich consisted of a half pack of cigarettes a day for 25 years.Initial vital signs were significant for hypertension. Physicalexam on presentation was significant for minimal epigastrictenderness with normoactive bowel sounds without reboundor guarding. Lab analysis was not significant for elevatedlipase, liver function abnormalities, anemia, or electrolyteabnormalities. Computed tomography (CT) of the abdomenand pelvis with IV contrast was performed which showeda filling defect in the celiac artery. Due to concern fordissection, a CT angiogram of the abdomen and pelvis wasperformed. The CT angiogram showed a 40.1mm dissectionfrom the celiac origin into the hepatic artery as well as a37.9mm dissection from the celiac origin into the splenic

artery (Figures 1 and 2). He was also found to have abeaded-appearing left main renal artery, raising concerns forfibromuscular dysplasia.

The patient was admitted for observation, given 1000mLunfractionated heparin bolus, and started on an unfraction-ated heparin infusion. The patient was evaluated by vascularsurgeons and gastroenterologists. When given the choice forstenting the lesion for symptomatic control, he elected notto have the lesion stented. Prior to discharge he was startedon 81mg aspirin daily and a follow-up appointment withrepeat CT angiography was scheduled in 2 months. Follow-up CT angiogram two months after his initial diagnosisshowed minimal enlargement of the dissection. At that timeduring his vascular surgery follow-up, the patient statedimprovement in his abdominal pain. At that time he wasscheduled for a 6-month appointment and follow-up CTA.

2. Discussion

Visceral artery dissection typically occurs as a complicationof an extension of a descending aortic dissection. However,spontaneous isolated visceral artery dissection has beendescribed in the literature.The prevalence and etiology of thisdisease are unknown as it is uncommon and the literatureconsists only of case reports and case series. Spontaneousdissection of the superior mesenteric artery is most common,

HindawiCase Reports in Emergency MedicineVolume 2017, Article ID 3704348, 3 pageshttps://doi.org/10.1155/2017/3704348

Page 2: Spontaneous Isolated Visceral Artery Dissection in a ... · CaseReport Spontaneous Isolated Visceral Artery Dissection in a Middle Aged Male EricMelnychukandRobertStrony DepartmentofEmergencyMedicine,GeisingerMedicalCenter,100NorthAcademyAvenue,Danville,PA17822,USA

2 Case Reports in Emergency Medicine

Figure 1: CT angiogram showing length of dissection of the celiacartery to the splenic vein.

followed by celiac artery dissection [1–3]. Patient characteris-tics typically include male gender, age over 50, hypertension,and history of smoking. However, spontaneous celiac arterydissection has been reported in younger, healthy patients [4].Treatment is not well defined and is currently tailored tothe patient’s severity of dissection and risk of progression[4, 5]. Observation with or without anticoagulation and closefollow-up, including serial imaging studies, may be effectivefor patients without signs of intestinal infarction or bleeding[3].

The most common sign of spontaneous visceral arterydissection is acute onset epigastric or abdominal pain not pre-ceded by trauma. Associated symptoms may include nausea,vomiting, or diarrhea [6–8]. Patients may have tendernessto abdominal palpation but usually do not exhibit peritonealsigns. Contrast-enhanced abdominal CT is the imagingmodality of choice and the most common imaging findingsare presence of an intimal flap, false lumen thrombosis, oraneurysmal dilatation [2, 9]. Misdiagnosis can occur evenwith contrast-enhanced CT [10]. Radiological classificationfor further characterization of SMA dissections was reportedin 2007 and included presence of a false lumen with orwithout reentry into the true lumen and thrombosis of thefalse lumen with or without a blood-filled pouch bulgingfrom the true lumen into a thrombosed false lumen [8].This classification system has subsequently been used forcharacterization of celiac artery dissections as well.

Complications of visceral arterial dissection includeintestinal ischemia or infarction from stenosis of the truelumen, aneurysm formation due to vessel wall degeneration,and vessel rupture. Initial conservative medial managementwith anticoagulation and close follow-up can be applied in theabsence of bowel ischemia or vessel rupture. Anticoagulationis thought to prevent vessel thrombosis and embolization.Surgicalmanagement with endovascular stenting can be usedin patients with persistent abdominal pain. Open surgicalmanagement is rare and is typically used when the dissectedvessel has ruptured.

Figure 2: CT angiogram reconstruction of the celiac artery at thetime of diagnosis.

Competing Interests

The authors disclose no conflict of interests.

References

[1] J. Y. Choi and O. J. Kwon, “Approaches to the managementof spontaneous isolated visceral artery dissection,” Annals ofVascular Surgery, vol. 27, no. 6, pp. 750–757, 2013.

[2] S. C. Jung, W. Lee, E.-A. Park, H. J. Jae, J. W. Chung, and J.H. Park, “Spontaneous dissection of the splanchnic arteries:CT findings, treatment, and outcome,” American Journal ofRoentgenology, vol. 200, no. 1, pp. 219–225, 2013.

[3] S. H. Ko, R. Hye, and D. A. Frankel, “Management of spon-taneous isolated visceral artery dissection,” Annals of VascularSurgery, vol. 29, no. 3, pp. 470–474, 2015.

[4] W.W. Zhang, J. D. Killeen, J. Chiriano, C. Bianchi, T. H. Teruya,and A. M. Abou-Zamzam, “Management of symptomaticspontaneous isolated visceral artery dissection: Is emergentintervention mandatory?” Annals of Vascular Surgery, vol. 23,no. 1, pp. 90–94, 2009.

[5] S. Alcantara, C. K. Yang, J. Sasson et al., “The evidence fornonoperative management of visceral artery dissections: asingle-center experience,” Annals of Vascular Surgery, vol. 29,no. 1, pp. 103–108, 2015.

[6] T. C. Ozturk, S. Yaylaci, O. Yesil, S. E. Cevik, and O. Guney-sel, “Spontaneous isolated celiac artery dissection,” Journal ofResearch in Medical Sciences, vol. 16, no. 5, pp. 699–702, 2011.

[7] V. Neychev, E. Krol, and A. Dietzek, “Unusual presentation andtreatment of spontaneous celiac artery dissection,” Journal ofVascular Surgery, vol. 58, no. 2, pp. 491–495, 2013.

[8] H.-C. Wang, J.-H. Chen, C.-C. Hsiao, C.-M. Jeng, and W.-L.Chen, “Spontaneous dissection of the celiac artery: a case reportand literature review,” The American Journal of EmergencyMedicine, vol. 31, no. 6, pp. 1000.e3–1000.e5, 2013.

[9] I. Sakamoto, Y. Ogawa, E. Sueyoshi, K. Fukui, T. Murakami,and M. Uetani, “Imaging appearances and management ofisolated spontaneous dissection of the superior mesentericartery,” European Journal of Radiology, vol. 64, no. 1, pp. 103–110, 2007.

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Case Reports in Emergency Medicine 3

[10] A.-R. Zeina, A. Nachtigal, A. Mahamid, U. Soimu, I. Ashkenazi,and M. Oster, “Isolated spontaneous dissection of a visceralartery: a rare cause of epigastric pain,”Emergency Radiology, vol.22, no. 3, pp. 215–220, 2014.

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