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Arq Neuropsiquiatr 2011;69(3):570

570

Images in neurology

Periventricular pleomorphic xanthoastrocytoma (PXA)

An uncommon tumor at an atypical site

Vinicius Trindade Gonçalves

1

, Fabiano Reis

2

, Luciano de Souza Queiroz

3

, Verônica de Araújo Zanardi

2

he patient was a 15-year-old male with seizures.

Di-agnostic imaging demonstrated a solid-cystic expansive

lesion, centered on the white matter of the left

temporo-occipital paratrigonal region, with growth into the

ven-tricular system (Fig 1).

Histological analysis led to the diagnosis of

pleomor-phic xanthoastrocytoma (PXA) (Fig 2).

PXA is classically a tumor with a predilection for

su-pericial growth afecting young adults, and is rarely seen

in paratrigonal/intraventricular locations. he tumor in

this case may have arisen in and around the ventricle or

from subcortical white matter.

he patient has now been followed for ten years. he

tumor recurred after ive years without anaplastic

trans-formation. He appears to be free of disease at present.

REFERENCES

1. Crespo-Rodriguez AM, Smirniotopoulos JG, Rushing EJ. MR and CT im-aging of 24 pleomorphic xanthoastrocytomas (PXA) and a review of the literature. Neuroradiol 2007;49:307-315.

2. Fu YJ, Miyahara H, Uzuka T, et al. Intraventricular pleomorphic xanthoas-trocytoma with anaplastic features. Neuropathol 2010;30:443-448. 3. Giannini C, Scheithauer BW, Burger PC, et al. Pleomorphic

xanthoastrocy-toma: what do we really know about it? Cancer 1999;85:2033-2045. 4. Kepes JJ, Rubinstein U, Eng LF. Pleomorphic xanthoastrocytoma: a

distinc-tive meningocerebral glioma of young subjects with reladistinc-tively favorable prognosis. Cancer 1979;44:1839-1852.

5. Koeller KK, Henry JM. From the archives of the AFIP: supericial gliomas: radiologic-pathologic correlation. RadioGraphics 2001;21:1533-1556.

XANTOASTROCITOMA PLEOMÓRFICO PERIVENTRICULAR: UM TUMOR INCOMUM EM LOCALIZAÇÃO ATÍPICA

Clinics Hospital, School of Medical Sciences, State University of Campinas, Campinas SP, Brazil: 1Medicine Student, Department of Radiology; 2MD, PhD, Professor of

the Department of Radiology; 3MD, PhD, Professor of the Department of Pathology.

Correspondence: Fabiano Reis - Departamento de Radiologia, Faculdade de Ciências Médicas, Universidade Estadual de Campinas - Rua Tessália Vieira de Camargo 126 - CP 6111 - Cidade Universitária Zeferino Vaz - 13083-887 Campinas SP - Brazil. E-mail: fabianoreis2@gmail.com

Support: VT Gonçalves receive financial support by FAPESP.

Received 28 January 2011. Received in final form 17 February 2011. Accepted 24 February 2011.

Fig 2. [A] Multinucleated tumor cell featuring prominent nuclear atypia and abundant eosin-ophilic cytoplasm, reminiscent of gemistocytic astrocytes. [B] Aberrant cell with numerous cy-toplasmic vacuoles, possibly containing lipids. [C] Large areas of tumor formed by spindle cells in bundles, often with large hyperchromatic nu-clei. [D] Masson’s trichrome staining, revealing thick collagen fibers among the tumor cells. [E] Reticulin fibers distributed at sites similar to those of collagen ibers. [F] A xanthomatous three-nucleated tumor cell with cytoplasmic positivity for GFAP (glial fibrillary acidic pro-tein), thus demonstrating its astrocytic lineage.

Imagem

Fig 2.  [A] Multinucleated tumor cell featuring  prominent nuclear atypia and abundant  eosin-ophilic cytoplasm, reminiscent of gemistocytic  astrocytes

Referências

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