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
. 2010 Feb 26;15(2):84-7.
doi: 10.1186/2047-783x-15-2-84.

Giant plexiform neurofibroma with hemorrhage in cranio-maxillofacial region as depicted on CT and MRI

Affiliations
Case Reports

Giant plexiform neurofibroma with hemorrhage in cranio-maxillofacial region as depicted on CT and MRI

Y Feng et al. Eur J Med Res. .

Abstract

Plexiform neurofibroma (PN) is a rare benign tumor and a special subtype of neurofibromatosis type 1 (NF1). Though the incidence is low, giant PN of the craniomaxillofacial region could result in severe hemifacial hypertrophy which is known as a typical manifestation of NF1 in young children. Here, we retrospectively reported a giant plexiform neurofibroma with hemorrhage in the cranio-maxillofacial region detected by CT and MRI. In addition, a brief review of the relevant literature is presented.

PubMed Disclaimer

Figures

Figure 1
Figure 1
A 21-year-old man with plexiforma neurofibroma in the right cranio-maxillofacial region. (A) Non-enhanced CT demonstrates a giant cystic-solid mass in the right craniomaxillofacial region, and the cyst of the mass appearing as hyper- and iso- attenuation (white arrows). (B) Contrast-enhanced CT depicts the mass appearing as no enhancement (arrows). (C) SSD reconstruction CT shows the cosmetic impairment of right face. (D) On T1-weighted MR image, the cyst of the mass shows heterogeneously intermediate to high signal intensity (arrows). (E) The cyst of the mass shows light low to intermediate signal intensity on T2 weighted MR image (arrowhead) with a low-signal ring around the hematoma (thin arrows).
Figure 2
Figure 2
Photomicrography of the case mention in figure 1. (A) Histology specimen demonstrates that the tumor is consisted of spindle-like schwann cells (arrow) (HE 200 ×), and (B) the area of hemorrhage in the mass (*, HE 100 ×).

Similar articles

Cited by

References

    1. Overdiek A, Feifel H, Schaper J, Mayatepek E, Rosenbaum T. Diagnostic delay of NF1 in hemifacial hypertrophy due to plexiform neurofibromas. No To Hattasu (Brain and Development) 2006;28(5):275–280. - PubMed
    1. Wise JB, Patel SG, Shah JP. Management issues in massive pediatric facial plexiform neurofibroma with neurofibromatosis type 1. Head Neck. 2002;24:207–211. doi: 10.1002/hed.10001. - DOI - PubMed
    1. Hersh JH. Health supervision for children with neurofibromatosis. Pediatrics. 2008;21:633–642. - PubMed
    1. Cre'ange A, Zeller J, Rostaing-Rigattieri S, Brugie'res P, Degos JD, Revuz J. et al.Neurological complications of neurofibromatosis type 1 in adulthood. Brain. 1999;122:473–481. doi: 10.1093/brain/122.3.473. - DOI - PubMed
    1. Malagari K, Drakopoulos S, Brountzos E, Sissopulos A, Efthimidadou A, Hadjiyiannakis E. et al.Plexiform neurofibroma of the liver: findings on MR imaging, angiography, and CT portography. AJR. 2001;176:493–495. - PubMed

Publication types