Elsevier

Clinical Imaging

Volume 38, Issue 5, September–October 2014, Pages 611-615
Clinical Imaging

Original Article
Magnetic resonance imaging findings of intracranial papillary meningioma: a study on eight cases

https://doi.org/10.1016/j.clinimag.2014.04.017Get rights and content

Abstract

Objectives

To increase the awareness on intracranial papillary meningiomas (PMs) by presenting magnetic resonance imaging (MRI) findings on this disease.

Materials and methods

The MRI findings and clinical presentations of nine discrete lesions in eight patients with pathologically documented PMs were retrospectively analyzed.

Results

Most tumors occurred in young adults. The tumors originated from the convexity meninges in five cases and from the parasagittal regions in four cases. The tumor shape was irregular in six cases, lobulated in two cases, and round in one case. By MRI, nine masses were primarily isointense (n=5) or mildly hypointense (n=4) to gray matter on T1-weighted images and inhomogeneous hyperintense (n=3) or isointense (n=6) to the cortex on T2-weighted and fluid-attenuated inversion recovery images. On diffusion-weighted imaging, the signal intensity of the tumor was increased in all lesions compared with the adjacent parenchyma. Tumor and brain interfaces were unclear in seven cases, cyst formation was observed in eight tumors, scattered hemorrhage was observed in three tumors, signal voids due to vessels were visible in four cases, and eight tumors had moderate or marked irregular peritumoral edema. Enhancement was homogeneous (n=2) or heterogeneous (n=7), an area of focal nodular enhancement was observed in three lesions, and the dural tail sign was visible in seven cases.

Conclusion

Although PM is rare, it should be considered in the differential diagnosis when evaluating intracranial neoplasms. Younger patient age, as well as imaging features such as unclear tumor–brain interface, internal heterogeneity including cyst formation, irregular enhancement, signal voids of vessels, and marked peritumoral edema can help distinguish PM from typical benign meningiomas.

Introduction

Meningiomas are common neoplasms accounting for approximately 13% to 19% of all primary intracranial tumors, represent a wide biological and histological spectrum, and generally have a favorable prognosis [1]. However, intracranial papillary meningioma (PM) is a rare, distinctive malignant histological variant of meningioma that has a higher incidence of recurrence and invasion or metastasis than other benign variants of meningioma [2], [3], [4]. Owing to the aggressive clinical course and poor prognosis of PM, a timely recognition of the diagnosis is desirable and helpful for rationalizing approaches to therapy.

Previous reports have concentrated on the histogenetic, histopathological, and clinical characteristics of PMs [1], [2], [3], [4], [5], [6], but only sporadic case reports have been able to describe imaging findings on PMs [7]. The purpose of the present study is to analyze the magnetic resonance imaging (MRI) findings and describe the clinical features of PMs.

Section snippets

Materials and methods

Approval of the institutional review board was obtained, and the requirement for patient consent was waived for this retrospective study. A retrospective review was performed from December 2007 to February 2010 at Huashan Hospital on eight patients with surgically and histologically proven PM. The patients included five men and three women ranging from 24 years to 54 years of age, with a median age of 35 years at first diagnosis.

MRI was performed in all eight patients using a 1.5 T MRI unit

Results

The clinical and MRI findings of all patients are summarized in Table 1. The median age of the patients was 35 years with a male to female ratio of 5:3. Most patients exhibited symptoms, including headache (n=5), epileptic seizures (n=3), and dizziness (n=2). Other presenting symptoms included hemiparesis (n=1), vomiting (n=1), tinnitus (n=1), and blurred vision (n=1). Symptom duration ranged from 2 weeks to 4 months, with an average of 2 months. Six patients had primary PMs, and the two other

Discussion

PM is a rare, distinctive malignant histological variant of meningioma with an incidence of 1.0% to 2.5% of all intracranial meningiomas [6], [7]. It was first described in 1938 by Cushing and Eisenhardt [8] as a papillary pattern in a meningioma showing intracerebral recurrence and pulmonary metastasis.

Histopathological examination revealed a tumor composed of sheets of cells arranged in a perivascular pseudopapillary pattern, along with a few well-formed papillae with a central fibrovascular

References (32)

  • B Pasquier et al.

    Papillary meningioma. Clinicopathologic study of seven cases and review of the literature

    Cancer

    (1986)
  • JF Lirng et al.

    MRI of papillary meningiomas in children

    Pediatr Radiol

    (1995)
  • H Cushing et al.

    Meningiomas: their classification, regional behavior, life history and surgical end results

    (1938)
  • JP Kim et al.

    Papillary meningioma with leptomeningeal seeding

    J Korean Neurosurg Soc

    (2011)
  • A Perry et al.

    Meningiomas

  • C Thomas et al.

    Papillary (malignant) meningioma of the foramen magnum presenting as a posterior neck mass

    Skull Base Surg

    (1994)
  • 1

    Xiang-Rong Yu and Jun-Zhang contributed equally to this work.

    View full text