PDF

Documento descargado de http://www.elsevier.es el 16/11/2016. Copia para uso personal, se prohíbe la transmisión de este documento por cualquier medio o formato.
Rev Esp Med Nucl Imagen Mol. 2013;32(4):275–276
Interesting images
Schwannomatosis/neurofibromatosis type 2 associated multiple schwannomas
visualized on FDG-PET/CT
Schwannomatosis/neurofibromatosis tipo 2 en FDG PET/TC de un paciente con múltiples
schwannomas
V. Beylergil ∗ , S. Haque, A. Carver, M.H. Bilsky, J.A. Carrasquillo
Memorial Sloan Kettering Cancer Center, New York, United States
a r t i c l e
i n f o
Article history:
Received 9 January 2013
Accepted 8 February 2013
Available online 11 April 2013
We present a patient with neurocutaneous syndrome, status
prior resections for cervical schwannomas and median as well
as radial nerve schwannomas. This is a 57-year-old female with
neurocutaneous syndrome presenting at 42 years of age with
unilateral vestibular schwannoma. Genetic testing was negative
but on clinical criteria neurofibromatosis-2 (NF-2) or schwannomatosis were considered.1 She underwent FDG PET/CT 85 min after
intravenous injection of 11.3 mCi (418.1 MBq) FDG, for recent onset
of severe left back pain with suspected cauda equina compression.
Whole-body FDG PET/CT showed multiple FDG avid soft tissue foci
overlying the sciatic nerve, consistent with multiple schwannomas
(Fig. 1). It also demonstrated heterogenous uptake corresponding
to multiple lesions visualized on MRI (Fig. 2).
Schwannomatosis can be hard to differentiate from NF-2 and
some authors suggested that vestibular schwannomas utilized
in the Manchester criteria,1 should not be an exclusion criterion
for the diagnosis of schwannomatosis. NF-2 is a rare autosomal
dominant syndrome that may have MERLIN gene mutation and/or
characterized by vestibular schwannomas, and other schwannomas, multiple meningiomas, ependymoma and lens opacities.
Neurofibromatosis type 1 (NF-1), on the other hand, is a different
disease with a few overlapping features.1 In contrast to NF-2
where malignant transformation is rare, NF-1 has 10% cumulative
incidence of malignant transformation2 thus several reports have
described the use of FDG in NF-1 to differentiate between benign
peripheral nerve sheath tumors (PNST) and malignant PNST.
Fig. 1. Whole-body FDG PET/CT showed (A–C) a series of FDG avid lesions overlying the left sciatic nerve (arrows) confirmed on MRI measuring up to 2.7 cm × 2.2 cm and
SUVmax whole body weight of 3.3, 3.2 and 3.1. In addition, hypermetabolic lesions were seen in left axilla and right shoulder (SUVmax of. 4.6 and 4.3, respectively), consistent
with schwannomas on MRI (data not shown).
∗ Corresponding author.
E-mail address: beylergv@mskcc.org (V. Beylergil).
2253-654X/$ – see front matter © 2013 Elsevier España, S.L. and SEMNIM. All rights reserved.
http://dx.doi.org/10.1016/j.remn.2013.02.005
Documento descargado de http://www.elsevier.es el 16/11/2016. Copia para uso personal, se prohíbe la transmisión de este documento por cualquier medio o formato.
276
V. Beylergil et al. / Rev Esp Med Nucl Imagen Mol. 2013;32(4):275–276
Fig. 2. FDG PET/CT also showed heterogenous uptake in the spinal canal (SUV 4.1) (A–C) that corresponded to additional lesions (arrows) on T1 contrast MRI (D).
Our report is unique in showing histologically proven intra
spinal canal schwannomas associated with neurocutaneous syndrome related to NF-2 or schwannomatosis. FDG uptake was in
the range described for benign PNST and some malignant PNST.
In our patient, given that there are multiple sites with same
intensity of FDG uptake malignant transformation of any lesion
was unlikely. This rare case also illustrates why close attention should be paid to the spinal canal (Fig. 2A–D) in these
patients, since these lesions can easily be mistaken for physiologic uptake in the distal spinal cord. Furthermore FDG may
detect other sites of schwannomas, as seen in this patient’s sciatic
nerve.
A single case report of FDG uptake in an intraspinal canal
schwannoma has been reported.3
Because these lesions were consistent with her pain distribution, she underwent T11-L2 partial laminectomy and removal of
histologically confirmed benign intradural schwannomas, with resolution of pain symptoms.
References
1. Uhlmann EJ, Plotkin SR. Neurofibromatoses. Adv Exp Med Biol. 2012;724:266–77.
2. Ferner RE, Golding JF, Smith M, Calonje E, Jan W, Sanjayanathan V, et al. [F18]2-fluoro-2-deoxy-d-glucose positron emission tomography (FDG PET) as a
diagnostic tool for neurofibromatosis 1 (NF1) associated malignant peripheral nerve sheath tumours (MPNSTs): a long-term clinical study. Ann Oncol.
2008;19:390–4.
3. Wilmshurst JM, Barrington SF, Pritchard D, Cox T, Bullock P, Maisey M, et al.
Positron emission tomography in imaging spinal cord tumors. J Child Neurol.
2000;15:465–72.