Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Case Reports
. 2013 Apr;78(2):50-3.
doi: 10.12659/PJR.883945.

Giant congenital malformation of the perirectal plexus in computed tomography imaging - case report

Affiliations
Case Reports

Giant congenital malformation of the perirectal plexus in computed tomography imaging - case report

Bartłomiej Kędzierski et al. Pol J Radiol. 2013 Apr.

Abstract

Background: Congenital arteriovenous malformation (AVM) in the pelvic area is uncommon in males.

Case report: The described case is of a giant lesion of this type that caused recurrent hemorrhaging in the lower part of the gastrointestinal tract. Preliminary diagnosis of vascular pathology was made on the basis of an endoscopic examination that revealed numerous pulsating protuberances of the rectal wall, in which blood flow was identified by means of transrectal ultrasonography. Complementing the diagnostics with a CT revealed a considerable extent of malformation, as well as its morphology and anatomical relations with the surrounding tissues.

Results: Following a two-year follow-up period, the malformation did not progress or demonstrate any intensification of clinical symptoms, therefore the patient continues to undergo conservative treatment.

Keywords: 3D reconstructions; Pelvic arteriovenous malformation (pAVM); computed tomography angiography (angio-CT); lower gastrointestinal tract bleeding; spiral computed tomography (CT).

PubMed Disclaimer

Figures

Figure 1
Figure 1
Colonoscopy: visible numerous, pulsating protuberances in rectal wall covered with smooth, glossy mucous membrane with a widened network of submucosal vessels.
Figure 2
Figure 2
CT examination, VRT reconstructions, anterior (A) and right-hand view (B): visible arteriovenous malformation filling a considerable part of the small pelvis.
Figure 3
Figure 3
CT examinations, MPR reconstruction, frontal plane. The image of pelvic AVM in CT examination performed approximately two years later (B) shows no essential changes in comparison with the initial examination (A).

References

    1. Richter GT, Friedman AB. Hemangiomas and vascular malformations: current theory and management. Int J Pediatr. 2012;2012:645678. - PMC - PubMed
    1. Game X, Berlizot P, Hassan T, et al. Congenital pelvic arteriovenous malformation in male patients: a rare cause of urogenital symptoms and role of embolization. Eur Urol. 2002;42(4):407–12. - PubMed
    1. Calligaro KD, Sedlacek TV, Savarese RP, et al. Congenital pelvic arteriovenous malformations: long-term follow-up in two cases and a review of the literature. J Vasc Surg. 1992;16(1):100–8. - PubMed
    1. Giambersio AM, Barile V, Alpi G, et al. Complex congenital pelvic vascular malformations in the male: a rare cause of andrological symptoms. A case report and review of the literature. J Androl Sci. 2010;17:67–69.
    1. Narvaez J, Narvaez JA, Alegre-Sancho JJ, et al. Pelvic arteriovenous malformation as a rare cause of sciatica. Br J Rheumatol. 1997;36(12):1340–41. - PubMed

Publication types

LinkOut - more resources