Primary rhabdomyosarcoma of the brain: observations on a case with clinical and radiological evidence of cure

P Celli, L Cervoni, C Maraglino - Journal of neuro-oncology, 1998 - Springer
Cerebral rhabdomyosarcoma is a highly aggressive tumor with poor prognosis affecting
children and, rarely, adults. The authors describe the case of a patient treated for primary …

Primary intracerebral mesenchymal chondrosarcoma with rhabdomyosarcomatous differentiation: case report and literature review

LAG Marshman, L Gunasekera, PE Rose… - British journal of …, 2001 - Taylor & Francis
Intracranial chondrosarcoma (Ch-S) is a slow-growing, locally recurrent, malignant
cartilaginous tumour of the skull base. Intracranial mesenchymal chondrosarcoma (MsCh-S) …

Radiation-induced rhabdomyosarcoma of the brainstem in a patient with neurofibromatosis Type 2: case report

ML Carlson, D Babovic-Vuksanovic, L Messiaen… - Journal of …, 2010 - thejns.org
Neurofibromatosis Type 2 (NF2) is a rare autosomal dominant disorder characterized by the
development of benign tumors of the peripheral nervous system and the CNS, including …

Primary intracranial soft tissue sarcoma in children and adolescents: a cooperative analysis of the European CWS and HIT study groups

M Benesch, AO von Bueren, T Dantonello… - Journal of neuro …, 2013 - Springer
Purely intracranial soft tissue sarcomas (ISTS) are very rare among children. A retrospective
database analysis of the Cooperative Weichteilsarkom Studiengruppe (CWS) and brain …

Intrasellar rhabdomyosarcoma: case report

K Arita, K Sugiyama, A Tominaga, F Yamasaki - Neurosurgery, 2001 - journals.lww.com
OBJECTIVE AND IMPORTANCE: There has been only one reported case of an intrasellar
rhabdomyosarcoma, the origin of which was in the paranasal sinus. The authors …

Successful treatment of primary intracranial sarcoma with the ICE chemotherapy regimen and focal radiation in children

L Lafay-Cousin, G Lindzon, MD Taylor… - Journal of …, 2016 - thejns.org
OBJECT Primary CNS sarcomas are very rare pediatric tumors with no defined standard of
care. METHODS This study was a retrospective review of children diagnosed with a primary …

Treatment strategy and long-term outcomes of primary intracranial rhabdomyosarcoma: a single-institution experience and systematic review

JJ Zheng, GJ Zhang, XL Huo, L Wang, SY Hao… - Journal of …, 2019 - thejns.org
OBJECTIVE Primary intracranial rhabdomyosarcoma (PIRMS) is rare, and the effects of the
treatment strategy on overall survival (OS) are unclear. This study aimed to evaluate risk …

Primary pineal rhabdomyosarcoma successfully treated by high-dose chemotherapy followed by autologous peripheral blood stem cell transplantation: case report

Y Ishi, S Yamaguchi, A Iguchi, Y Cho… - Journal of …, 2016 - thejns.org
Primary intracranial rhabdomyosarcoma is quite rare, and its prognosis is poor compared
with that for rhabdomyosarcoma in other organs. The authors present a case of pineal …

Successful treatment of a child with a primary intracranial rhabdomyosarcoma with chemotherapy and radiation therapy

GMT Guilcher, G Hendson, K Goddard… - Journal of Neuro …, 2008 - Springer
Primary rhabdomyosarcoma of the central nervous system (CNS) is rare in both adults and
children (Taratuto et al.(1985) Acta Neuropathol (Berl) 66 (2): 98–104). The outcome in the …

Signet-ring cell oligodendroglioma–report of two cases and discussion of the differential diagnosis

JM Kros, WA van den Brink, JJML Luyt… - Acta …, 1997 - Springer
Two cases of oligodendroglioma consisting largely of signet-ring cells were analyzed
histopathologically, immunohistochemically and at the ultrastructural level. The signet-ring …