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A 28-YEAR-OLD MAN WITH HEADACHE, VISUAL AND APHASIC SPEECH DISTURBANCES
Frank, Stephan ; Cordier, Dominik ; Tolnay, Markus ; Rosenblum, Marc K.
Brain pathology (Zurich, Switzerland), 2009-01, Vol.19 (1), p.163-166
[Peer Reviewed Journal]
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Title:
A 28-YEAR-OLD MAN WITH HEADACHE, VISUAL AND APHASIC SPEECH DISTURBANCES
Author:
Frank, Stephan
;
Cordier, Dominik
;
Tolnay, Markus
;
Rosenblum, Marc K.
Subjects:
Adult
;
Antigens
,
CD34
-
analysis
;
Aphasia - etiology
;
Brain Neoplasms - complications
;
Brain Neoplasms - diagnosis
;
Brain Neoplasms - metabolism
;
Correspondence
;
Gliosarcoma - complications
;
Gliosarcoma - diagnosis
;
Gliosarcoma - metabolism
;
Headache - etiology
;
Humans
;
Immunohistochemistry - methods
;
Magnetic Resonance Imaging
;
Male
;
Neoplasm Recurrence, Local
Is Part Of:
Brain pathology (Zurich, Switzerland), 2009-01, Vol.19 (1), p.163-166
Description:
A 28-year-old man presented with a short history of headache, visual and aphasic speech disturbances. MR scans revealed a large, partly cystic, contrast-enhancing lesion of the left temporal lobe that upon microscopic examination was diagnosed as pleomorphic xanthoastrocytoma (PXA) with anaplastic features (WHO grade III). Remarkably, this tumor featured an unusual gliovascular, rosette-like histoarchitecture, which had previously been hypothesized to possibly indicate a greater likelihood of PXA recurrence. Indeed, only 14 months later, the patient presented with a recurrent lesion, which contained the previous histology, but now also featured a distinct fibrosarcoma-like component replete with numerous osteoclast-type giant cells. In addition, whereas eosinophilic granular bodies were plentiful at the lesion's periphery, numerous
CD34
- positive satellite cells were found in the adjacent non-infiltrated cortex. Regarding the origin of this recurrent tumor and in reflection of its composition of distinct PXA as well as sarcomatous components, the diagnosis of a pleomorphic xanthoastrosarcoma, to be conceptually considered as a gliosarcoma subtype, was made.To our knowledge, this is an unprecedented case of sarcomatous transformation of a PXA. Particular attention should be given to gliovascular pseudopapillary structures in PXAs, the presence of which may potentially herald a more aggressive clinical behavior.
Publisher:
Oxford, UK: Blackwell Publishing Ltd
Language:
English
Identifier:
ISSN: 1015-6305
EISSN: 1750-3639
DOI: 10.1111/j.1750-3639.2008.00241.x
PMID: 19076784
Source:
Wiley Online Library All Journals
Wiley Online Library Full Collection 2020
Links
View this record in MEDLINE/PubMed
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