Pregled bibliografske jedinice broj: 119445
BIHEMISPHERICAL CEREBRAL GANGLIOGLIOMA AND HEMANGIOMATOUS MALFORMATION IN AN 18-MONTH-OLD-CHILD ; CASE REPORT
BIHEMISPHERICAL CEREBRAL GANGLIOGLIOMA AND HEMANGIOMATOUS MALFORMATION IN AN 18-MONTH-OLD-CHILD ; CASE REPORT // The 10th "Ljudevit Jurak" International Symposium on Comparative Pathology, Zagreb, June 4 - 5th, 1999 : book of abstracts / Talan Hranilović, Jasna ; Krušlin, Božo (ur.).
Zagreb: [Academy of Medical Sciences of Croatia], 1999. (poster, domaća recenzija, sažetak, stručni)
CROSBI ID: 119445 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
BIHEMISPHERICAL CEREBRAL GANGLIOGLIOMA AND HEMANGIOMATOUS MALFORMATION IN AN 18-MONTH-OLD-CHILD ; CASE REPORT
Autori
Kogler, Andrej ; Radić, I. ; Talan-Hranilović, Jasna ; Božić, Boris
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, stručni
Izvornik
The 10th "Ljudevit Jurak" International Symposium on Comparative Pathology, Zagreb, June 4 - 5th, 1999 : book of abstracts
/ Talan Hranilović, Jasna ; Krušlin, Božo - Zagreb : [Academy of Medical Sciences of Croatia], 1999
Skup
The 10th "Ljudevit Jurak" International Symposium on Comparative Pathology
Mjesto i datum
Zagreb, Hrvatska, 04.06.1999. - 05.06.1999
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
bihemispherical cerebral ganglioglioma
Sažetak
In this paper a rare case of concomitant bihemispherical cerebral ganglioglioma and hemangiomatous malformation in an 18-month-old boy is presented. Gangliogliomas are relatively uncommon tumours in childhood. They consist of a mixture of glial cells and differentiated nerve cells, and represent true neoplasms with the potential for progressive growth. The child underwent diagnostic neuroimaging examinations (CT and MRI) for seizures and right-sided facial palsy that showed the bilaterally presence of parieto-occipital, oval, well demarcated, subcortically processes. A biparieto-occipital craniotomy was carried out and two well-demarcated abnormalities were detected and removed in toto. Three years after the operation, the boy experienced normal psychomotor development and remained free from seizures with no therapy required. Repeat MRI showed no tumour recurrence. Histopathologic and immunohistochemical analysis of the two processes found in our patient showed them to be a ganglioglioma and a hemangiomatous malformation, confirming the dysontogenetic origin of these alterations and association between malformations and tumour growth. The combination of ganglioglioma and hemangiomatous malformation, especially bilateral presentation of such two identical processes in a young child is very rare and was not found in the recent literature.
Izvorni jezik
Engleski
Znanstvena područja
Kliničke medicinske znanosti
POVEZANOST RADA
Ustanove:
KBC "Sestre Milosrdnice"