Literature DB >> 30713380

A Patient with a Benign and a Malignant Primary Pulmonary Meningioma: An Evaluation with 18F Fluorodeoxyglucose Positron Emission Tomography/Computed Tomography and Computed Tomography with Iodinated Contrast.

Andrea Cimini1, Francesca Ricci1, Luca Pugliese1, Agostino Chiaravalloti1,2, Orazio Schillaci1,2, Roberto Floris1.   

Abstract

An 80-year-old male with a previous history of thymoma and kidney cancer underwent a 18F fluorodeoxyglucose (FDG) positron emission tomography (PET)/contrast-enhanced computed tomography (CT) scan: two pulmonary nodules were discovered, both characterized by an increased glucose uptake. Of them, only one showed mild contrast enhancement. Both nodules were surgically resected: the first nodule was a benign meningioma and the second one was a malignant meningioma. This case study shows that malignancy of meningioma in the lung is not correlated with 18F FDG uptake and the contrast enhancement, thus suggesting that PET/CT may represent a suboptimal imaging modality for the evaluation of these lesions.

Entities:  

Keywords:  18F fluorodeoxyglucose; ectopic meningioma; iodinated contrast enhancement; malignant meningioma; pulmonary nodule

Year:  2019        PMID: 30713380      PMCID: PMC6352649          DOI: 10.4103/ijnm.IJNM_101_18

Source DB:  PubMed          Journal:  Indian J Nucl Med        ISSN: 0974-0244


Introduction

Ectopical meningiomas (extracranial meningiomas) are extremely rare: despite being one of the most frequently diagnosed primary intracranial tumors, meningioma rarely occurs in several locations such as the head-and-neck region, skin, bone, peripheral nerves, retroperitoneum, and lung.[12] Different histogenetic and pathologic mechanisms have been proposed, but the true etiology of this tumor is still uncertain:[3] Some authors believe that extracranial meningioma might derive from misplaced or migrate arachnoid cells, other investigators have revealed that the tumor may originate from perineurial cells or pluripotent mesenchymal cells.[2] The first reported case of primary pulmonary meningioma (PPM) was in 1982.[4] To the best of our knowledge, till date, only 44 cases have been reported in the literature: among these cases, only five were malignant or atypical.[12]

Case Report

An 80-year-old male, from whom we obtain the consent form, during the follow-up for thymoma (previous thymectomy in 2011) and kidney cancer (previous nephrectomy in 2012), presented a solitary pulmonary nodule in the superior lobe of the right lung as detectable by means of 18F fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) scan in December 2015 (injected dose 380 MBq). PET/CT images showed a metabolically active lesion (SUVmax 4.63 g/ml bw, 14 mm in diameter), suspected of being a metastasis [Figure 1]. Contrast-enhanced CT with iodinated contrast media performed after PET examination did not show significant attenuation between pre- and postcontrast phase [Figure 2]. After a right pulmonary resection in January 2016, bioptic diagnosis of the nodule was compatible with fibrotic (benign) pulmonary meningioma.
Figure 1

Positron emission tomography/computed tomography image of the fibrous (benign) pulmonary meningioma

Figure 2

Contrast-enhanced computed tomography image of the fibrous (benign) pulmonary meningioma

Positron emission tomography/computed tomography image of the fibrous (benign) pulmonary meningioma Contrast-enhanced computed tomography image of the fibrous (benign) pulmonary meningioma In June 2016, another 18F FDG PET/CT scan was performed in the same patient (injected dose 361 MBq) that showed another new metabolically active pseudonodular lesion (SUVmax 2.46 g/ml bw, 12 mm in diameter) in the superior lobe of the left lung [Figure 3]. A CT scan with iodinated contrast, the lesion showed enhancement at postcontrast phase [basal scan:-1 HU; postcontrast scan: 55 HU, Figure 4]. After an atypical resection of the superior lobe of the left lung in September 2016, biopsy showed a high proliferative activity with a number of mitotic figures >20/10 HPF, Ki-67 ≈ 20%, with associated necrosis and on immunohistochemistry cells expressed epithelial membrane antigen and they were positive for vimentin and progesterone: the final diagnosis was anaplastic meningioma (malignant).
Figure 3

Positron emission tomography/computed tomography image of the malignant pulmonary meningioma

Figure 4

Contrast-enhanced computed tomography image of malignant pulmonary meningioma

Positron emission tomography/computed tomography image of the malignant pulmonary meningioma Contrast-enhanced computed tomography image of malignant pulmonary meningioma

Discussion

To the best of our knowledge, this is the first 18F FDG PET/CT evaluation of a patient with synchronous benign and malignant PPM, with similar dimensions (14 and 12 mm in diameter): qualitative and semi-quantitative (SUVmax) analysis with PET suggested less metabolic activity in malignant PPM, with more intense uptake of 18F FDG in fibrotic PPM. Furthermore, anaplastic meningioma showed enhancement with iodinated contrast media. From this case report, we conclude that 18F FDG PET may not suffice in the evaluations of patients with PPM; the conjunction with contrast-enhanced CT may help in the discrimination between malign and benign lesions. Furthermore, due to high levels of expression of the somatostatin receptor subtype 2 in meningiomas, the use of other radiolabeled compounds (i.e., 68Ga-DOTATOC PET/CT[15]) may be more useful for this aim.

Declaration of Patient Consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

There are no conflicts of interest.
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