Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 2 de 2
Filter
Add more filters










Database
Language
Publication year range
1.
Childs Nerv Syst ; 23(5): 573-6, 2007 May.
Article in English | MEDLINE | ID: mdl-17053937

ABSTRACT

OBJECTIVE: Teratoma is the most frequently encountered intracranial tumor at birth and constitutes 18-20% of all germ cell tumors. They are usually located in pineal and suprasellar regions. The authors aim to report an extremely unusual presentation, location, and appearance of a teratoma in a newborn. CASE REPORT: A soft tissue swelling in the vertex was detected in a 1-month-old girl. Neurological examination was normal. A big, cystic-solid lesion beginning from pineal region and extending to the scalp was detected in magnetic resonance imaging. It is interesting to note that cerebral venous angiography showed that the superior sagittal sinus (SSS) was divided into three branches at the level of the lesion and they joined together distally. The tumor was excised totally. Histopathological examination revealed the diagnosis of a mature cystic teratoma. CONCLUSION: A mature cystic teratoma mimicking parietal encephalocele is extremely rare. Germ cell tumors should be kept in mind in the differential diagnosis of all midline lesions with unusual radiographic appearance. Cerebral venous angiography or MR angiography must be performed for the diagnosis and the surgical planning in lesions located near SSS.


Subject(s)
Encephalocele/pathology , Parietal Lobe/pathology , Pinealoma/pathology , Teratoma/pathology , Cerebral Angiography , Diagnosis, Differential , Female , Humans , Infant , Magnetic Resonance Angiography , Magnetic Resonance Imaging , Neurosurgical Procedures , Pinealoma/congenital , Pinealoma/surgery , Teratoma/congenital , Teratoma/surgery
2.
J Pediatr Hematol Oncol ; 28(3): 173-6, 2006 Mar.
Article in English | MEDLINE | ID: mdl-16679944

ABSTRACT

We report a 2-year-old boy who had a family history of neurofibromatosis, multiple cafe-au-lait spots on the trunk, tibial pseudarthrosis, and was diagnosed with a malignant triton tumor of the pelvis. To our knowledge our case is one of the youngest patients reported with a malignant triton tumor and the second pediatric case with a pelvic malignant triton tumor.


Subject(s)
Neoplasm Recurrence, Local/pathology , Nerve Sheath Neoplasms/pathology , Neurofibromatosis 1/complications , Pelvis/pathology , Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Cafe-au-Lait Spots/etiology , Child, Preschool , Genetic Predisposition to Disease , Humans , Male , Neoplasm Recurrence, Local/physiopathology , Neoplasm Recurrence, Local/therapy , Nerve Sheath Neoplasms/physiopathology , Nerve Sheath Neoplasms/therapy , Pseudarthrosis/complications , Pseudarthrosis/congenital
SELECTION OF CITATIONS
SEARCH DETAIL
...