TY - JOUR
T1 - Melanotic neuroectodermal tumour of infancy
T2 - A rare brain tumour of childhood
AU - Khan, Muhammad Babar
AU - Soares, Delvene
AU - Tahir, Muhammad Zubair
AU - Kumar, Rajesh
AU - Minhas, Khurram
AU - Bari, Muhammad Ehsan
PY - 2013/5
Y1 - 2013/5
N2 - Melanotic neuroectodermal tumour of infancy is a rare, mostly benign but locally aggressive tumour of neural crest cell origin occurring in infants. The most commonly affected anatomic site is the maxilla. Such tumours of the brain and skull are very rare. We present the case of an 8 months old baby girl whose presenting complaint was a swelling in the scalp for 6 months. She was otherwise asymptomatic. CT imaging confirmed the presence of an osteolytic tumour in the anterior parasagittal skull with dural involvement. The tumour was surgically excised enbloc. The patient has been well at 2 years follow-up without any evidence of recurrence.
AB - Melanotic neuroectodermal tumour of infancy is a rare, mostly benign but locally aggressive tumour of neural crest cell origin occurring in infants. The most commonly affected anatomic site is the maxilla. Such tumours of the brain and skull are very rare. We present the case of an 8 months old baby girl whose presenting complaint was a swelling in the scalp for 6 months. She was otherwise asymptomatic. CT imaging confirmed the presence of an osteolytic tumour in the anterior parasagittal skull with dural involvement. The tumour was surgically excised enbloc. The patient has been well at 2 years follow-up without any evidence of recurrence.
KW - Enbloc tumour excision
KW - GFAP stain
KW - Melanotic neuroectodermal tumour
KW - Osteolytic pigmented lesion
KW - Scalp swelling
KW - Vanillylmandelic acid
UR - http://www.scopus.com/inward/record.url?scp=84877675853&partnerID=8YFLogxK
M3 - Article
C2 - 23673182
AN - SCOPUS:84877675853
SN - 1022-386X
VL - 23
SP - 367
EP - 369
JO - Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
JF - Journal of the College of Physicians and Surgeons--Pakistan : JCPSP
IS - 5
ER -