Case Reports in Radiology

Case Reports in Radiology / 2021 / Article

Case Report | Open Access

Volume 2021 |Article ID 8854806 |

Amir Pakray, Nolan Hayden, Farnoosh Sokhandon, Johnathan Olsen, "Detection and Intervention of Clinically Masquerading Inferior Mesenteric Artery AVMs", Case Reports in Radiology, vol. 2021, Article ID 8854806, 6 pages, 2021.

Detection and Intervention of Clinically Masquerading Inferior Mesenteric Artery AVMs

Academic Editor: Atsushi Komemushi
Received29 Aug 2020
Revised04 Apr 2021
Accepted18 May 2021
Published29 May 2021


We demonstrate a rare case of inferior mesenteric artery arteriovenous malformations leading to ischemic colitis in a 76-year-old female. Our patient presented with three months of nausea, vomiting, and diarrhea. Colonoscopy displayed diffuse mucosal vascular congestion while CTA and MRA displayed AVMs in the region of the IMA; however, cohesive clinical agreement on AVM from multiple specialties was difficult given its rare occurrence and nonspecific clinical, histopathologic, and directly visualized findings. The three noted dominant AVMs were eventually selected with coil and liquid embolization with successful cessation of symptoms and no major complications. Our discussion focuses on intervention and stressing the importance of radiologic findings, as IMA AVMs, rarely present as ischemic colitis and therefore can clinically masquerade as other etiologies.

1. Introduction

Ischemic colitis comprises over half of gastrointestinal ischemic insults and is most commonly noted in females, particularly over the age of 60 and with multiple comorbidities [1]. The most common and classic presentation of ischemic colitis is an acute onset abdominal pain, bloody stools, and leukocytosis. The patient in our case displayed the abovementioned demographics and some of the symptoms. Ischemic colitis can be classified into two categories of occlusive and nonocclusive etiologies. AVMs and AVFs fall underneath the umbrella of nonocclusive ischemic colitis; however, these are distinct entities with delineating factors, namely, that AVMs are typically congenital and AVFs are more often acquired [1]. Overall splanchnic vascular anomalies are rather rare with approximately 200 reported cases, and most notably the least common reported occurrence is in the IMA distribution, with hepatic and splenic territories more often encountered [1]. Therefore, the case we discuss highlights the rarest distribution of ischemic colitis from a vascular anomaly. Failure of undifferentiated embryonic vasculature regression is what leads to the typical imaging features of a dilated feeding artery, a nidus of tangled vessels and early draining veins [1]. Inferior mesenteric AVMs are typically accompanied by symptoms affiliated with portal hypertension such as ascites or variceal bleeding [24]. A smaller subset of patients display congestive ischemic colitis symptoms. Patients with congestive ischemic colitis due to inferior mesenteric AVMs present with abdominal pain, hematochezia, and diarrhea. Our case demonstrated this less common symptomatic array and presentation of AVM-induced ischemic colitis. As the clinical presentation of IMA AVMs can vary greatly, multiphase cross-sectional imaging plays a critical role in arriving at the correct diagnosis.

Current literature supports the use of MDCT angiography for initial evaluation of inferior mesenteric AVMs with subsequent colonoscopy in order to histopathologically exclude any masquerading disease [5]. Distribution and extent of disease is best assessed by utilizing MDCT angiography [1]. Although nonspecific, wall thickening or mural edema exhibited as a thickened hypodense appearance of the bowel wall is most commonly seen when ischemic colitis is encountered. Additional nonspecific findings include ascites and infiltration of the pericolonic mesenteric fat. All three of these imaging findings (bowel wall thickening, pericolonic mesenteric fat infiltration, and ascites) were noted on our case. Mucosal hypoperfusion and submucosal edema from arterial steal phenomenon and venous hypertension, respectively, explain the vascular mechanism behind congestive ischemic colitis [2, 6, 7].

Treatment is typically case-specific necessitating diagnostic consensus and clinical cohesion amongst various specialties including gastroenterology, vascular surgery, interventional radiology, and diagnostic radiology. Literature supports arterial embolization at the arteriovenous interface given its efficacy, noninvasive approach, and low complication rates [3, 8]. Athanasiou et al. suggest satisfying three criteria to prevent misdiagnosis and suboptimal intervention in cases suspected of ischemic colitis: first is identifying clinical signs of colonic ischemia, second is diagnostic imaging evaluation and confirmation of the etiology, in our case vascular malformation (ideally an angiogram), and third is direct visualization of a congested colonic mucosa via colonoscopy [9]. Larger and/or higher flow AVMs are directly associated with higher embolization complication rates [3, 8]. Embolization, although less invasive than surgical intervention, is not without risk. Embolization can cause organ ischemia and/or recurrence especially when more than one feeding vessel is identified [9]. The risk of nontarget embolization from particle migration has been noted to increase when a high-flow AVM displays a diameter larger than 8 mm [9]. Surgical intervention can potentially be curative; however, it is known to have higher risk of hemorrhage [9].

2. Case Presentation

Our patient is a 76-year-old female with a past medical history of hypertension, type 2 diabetes mellitus, hypothyroidism, and gastroesophageal reflux disease, initially presenting to the emergency department (ED) with a three-month history of nausea, vomiting, and occasional diarrhea. She was evaluated by gastroenterology, and an outpatient EGD was performed showing a small hiatal hernia and atrophic gastritis. Within the next few weeks, she presented to ED with acute onset abdominal pain and worsening diarrhea which now appeared to be bloody. A CT scan of abdomen and pelvis was requested for the clinical diagnosis of ischemic colitis. Significant colonic wall thickening and pericolonic inflammatory stranding of the entire colon with sparing of the cecum, concerning for pancolitis with mild ascites, were noted on the initial CT scan (Figures 1(a) and 1(b)). The gastroenterology team was mostly concerned for noninfectious colitis, namely, ulcerative colitis or ischemic colitis, and boarded her for colonoscopy. Due to the patient’s overall condition, comorbidities, and improvement of acute symptoms with supportive care, a colonoscopy was performed three days after admission when she was deemed stable. The results revealed pancolonic diffuse mucosal vascular congestion, pronounced in the rectosigmoid region, with a decreased mucosal vascular pattern. Random biopsies were performed which histopathologically revealed architectural distortion and paneth cell metaplasia, as seen in chronic colitis, without evidence of active colitis, granulomas, crypt abscesses, or dysplasia. The following day, a CTA of the abdomen and pelvis was obtained to evaluate for the possibility of an underlying vascular etiology. CTA showed that diffuse pancolitis slightly improved compared to the prior CT exam four days prior with a normal caliber patent abdominal aorta and proximal mesenteric vasculature. The CTA also displayed tortuous vascular lesions in the IMA territory with early filling veins concerning for AVMs (Figures 2(a)2(d)). Given the rarity of AVM-induced ischemic colitis, patency of proximal mesenteric vessels, biopsy results suggesting chronic colitis, and overall clinical improvement with supportive therapy and steroids, the clinical suspicion favored ulcerative colitis. Given this presumed diagnosis, steroid therapy was continued and the patient was discharged in stable condition with recommendation for a follow-up in two weeks. At the time of follow-up, the patient had no abdominal symptoms and reported complete improvement.

Approximately one month later, the patient presented to the emergency department with bilateral lower extremity edema and fatigue. Work-up for the edema revealed bilateral lower extremity DVTs, and the patient was placed on Lovenox. Shortly after, the patient developed several episodes of hematochezia and abdominal pain which prompted MRA of the abdomen, further strengthening the concern for AVMs. The MRA exhibited an inferior mesenteric artery distribution of multiple focal aneurysmal vessels in the left colonic mesentery (Figures 3(a) and 3(b)). Additionally, MRA displayed mild improvement in the patient’s previously noted colitis.

At this point, interventional radiology was consulted for a mesenteric angiogram. Arteriogram demonstrated a total of 3 AVMs, each individually supplied by branches of the IMA (Figures 4(a)4(d)). The left colic artery was divided into two distal omental branches, which were coil embolized prior to Onyx liquid embolic instillation of the left colic artery (Figure 5(a)). The superior rectal artery was divided into two distal branches; both of which supplied the largest of the three AVMs, which was embolized with Onyx injection into the superior rectal artery proximal to both of the aforementioned branches (Figure 5(b)). The sigmoid artery, similar to the left colic, had two distal omental branches that were coil embolized before Onyx liquid embolic instillation (Figure 5(c)). There was an enlarged marginal vein draining into the middle colic vein with increased flow due to the AVMs. Subsequent SMA arteriogram displayed adequate flow to the left colon, sigmoid colon, and superior rectum from collaterals supplied by the marginal artery.

During postprocedural follow-up, the patient denied any abdominal pain, melena, or hematochezia. The patient demonstrated stability for over 1 year and was without any recurrence of abdominal symptoms.

3. Discussion

This is a novel case for several reasons and elucidates the importance of utilizing multiphasic cross-sectional imaging for an accurate diagnosis given the rare presentation. As previously noted, IMA distribution of AVMs is the least common distribution of splanchnic vascular anomalies. Furthermore, instead of presenting with the more common portal hypertension-associated symptoms, our patient presented with the less common presentation of ischemic colitis with hematochezia and diarrhea.

Initial confusion in diagnosis occurred for several reasons in our case. Retrospective evaluation of the initial ED non-IV contrast CT abdomen and pelvis did display tortuous vasculature in the IMA distribution; however, given that no IV contrast was given, this finding can easily be overlooked. Colonoscopy showed mucosal vascular congestion, and histopathology revealed architectural distortion seen in chronic colitis; thus, an acute ischemic colitis was considered less likely. The subsequent CTA of the abdomen and pelvis did however delineate the vascular malformations very well. However, given the rarity of AVM-induced ischemic colitis and pathology findings, clinical management of chronic colitis was continued. This highlights the importance of scrutinizing the associated intestinal vasculature when bowel pathology is demonstrated. Multimodality multiphasic cross-sectional imaging (CTA and MRA) built a very strong diagnosis of IMA distribution AVMs, allowing visualization of the niduses in the arterial and venous phase along with any underlying vascular pathology that could preclude intervention. Mesenteric angiogram further confirmed the suspected three niduses in the IMA distribution. Additionally, the angiogram allowed the interventional team to deem the AVMs amenable to liquid and coil embolization as they did not appear too high flow or large for intervention.

This case report is limited due to the lack of postprocedural imaging which would allow for thorough evaluation of the vascular anatomy and collateralization, serving as a beneficial baseline if future complications were to arise. However, in our case, the patient had no complications in the postprocedural course, and therefore, imaging was not clinically indicated. The multimodality imaging of this case report (CT, CTA, MRA, and angiogram) allows for wholesome diagnostic and interventional evaluation and augments our understanding of a rare vascular anomaly.

Ischemic colitis secondary to AVMs can be strongly suggested and diagnosed on imaging, and with multispecialty diagnostic consensus can lead to early treatment and fewer complications. This elucidates that the imperative role of radiology can play in suggesting a firm diagnosis and providing appropriate intervention.

Data Availability

Full anonymized datasets (DICOM images, aside from the provided images in the case report) used to support the findings of this study are available from the corresponding author upon request.

Conflicts of Interest

The authors declare that they have no conflicts of interest.


  1. B. Coulier, J.-F. De Wispelaere, I. Bueres et al., “Acute massive congestive ischaemic colitis related to inferior mesenteric arteriovenous malformation,” BJR case reports, vol. 2, no. 1, 2016. View at: Publisher Site | Google Scholar
  2. A. I. Justaniah, C. Molgaard, S. Flacke, A. Barto, and S. Iqbal, “Congenital inferior mesenteric arteriovenous malformation presenting with ischemic colitis: endovascular treatment,” Journal of Vascular and Interventional Radiology, vol. 24, no. 11, pp. 1761–1763, 2013. View at: Publisher Site | Google Scholar
  3. K. Okada, N. Furusyo, Y. Sawayama et al., “Inferior mesenteric arteriovenous fistula eight years after sigmoidectomy,” Internal Medicine, vol. 41, no. 7, pp. 543–548, 2002. View at: Google Scholar
  4. P. D. Poullos, A. C. Thompson, G. Holz, L. A. Edelman, and R. B. Jeffrey, “Ischemic colitis due to a mesenteric arteriovenous malformation in a patient with a connective tissue disorder,” Journal of radiology case reports, vol. 8, no. 12, pp. 9–21, 2014. View at: Publisher Site | Google Scholar
  5. L. J. Brandt, P. Feuerstadt, G. F. Longstreth, and S. J. Boley, “ACG clinical guideline: epidemiology, risk factors, patterns of presentation, diagnosis, and management of colon ischemia (CI),” The American Journal of Gastroenterology, vol. 110, no. 1, pp. 18–44, 2015. View at: Publisher Site | Google Scholar
  6. E. C. Gorospe, C. L. Leggett, and G. Sun, “Inferior mesenteric arteriovenous malformation: an unusual cause of ischemic colitis,” Annals of Gastroenterology, vol. 25, p. 165, 2014. View at: Publisher Site | Google Scholar
  7. D. R. Metcalf, S. Nivatvongs, and J. C. Andrews, “Ischemic colitis: an unusual case of inferior mesenteric arteriovenous fistula causing venous hypertension. Report of a case,” Diseases of the colon & rectum, vol. 51, no. 9, pp. 1422–1424, 2008. View at: Publisher Site | Google Scholar
  8. N. Brucher, G. Moskovitch, P. Otal, X. Chaufour, and H. Rousseau, “Inferior mesenteric arteriovenous fistula treated by percutaneous arterial embolization: a breathtaking story!,” Diagnostic and interventional imaging, vol. 95, no. 1, pp. 85-86, 2014. View at: Publisher Site | Google Scholar
  9. A. Athanasiou, A. Michalinos, A. Alexandrou, S. Georgopoulos, and E. Felekouras, “Inferior mesenteric arteriovenous fistula: case report and world-literature review,” World Journal of Gastroenterology, vol. 20, no. 25, pp. 8298–8303, 2014. View at: Publisher Site | Google Scholar

Copyright © 2021 Amir Pakray et al. This 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.

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