scholarly journals Extraventricular Choroid Plexus Carcinoma with Spinal Metastasis: A Case Report

2021 ◽  
Vol 9 (C) ◽  
pp. 93-98
Author(s):  
Rachmat Andi Hartanto ◽  
Daniel Agriva Tamba ◽  
Nurhuda Hendra Setyawan ◽  
Ericko Ekaputra ◽  
Rusdy Ghazali Malueka ◽  
...  

We report a case of extraventricular choroid plexus carcinoma (CPC) accompanied by spinal metastasis in a pediatric patient. A 15-year-old female patient presented with chronic progressive headache and blurry vision. Magnetic resonance imaging (MRI) revealed an intra-axial mass in the left frontal lobe. A gross total resection was performed, and the histopathological examination revealed the diagnosis of CPC, confirmed with immunohistochemical (IHC) analysis of GFAP, S100, EM, P53 and Ki67. Eleven months later, MRI result identified another mass in the left frontal lobe. Spinal MRI showed drop metastasis to the spine, accompanied by leptomeningeal seeding. This case demonstrated the importance of IHC and spinal MRI in the management of CPC. This case report may provide more insight into extraventricular CPC cases, which is important for the adequate management of patients with CPC in the future.

2014 ◽  
Vol 40 (01) ◽  
pp. 63-68 ◽  
Author(s):  
Pin-Chieh Peng ◽  
Hue-Ying Chiou ◽  
Pin-Hsien Wu ◽  
Ya-Pei Chang ◽  
Peng-Cheng Wang

Choroid plexus tumors (PTs) are rare in dogs. Herein, we reported a canine case of choroid plexus carcinoma (CPC) and its clinical treatment. A 10-year-old male Shar Pei presented a two-month history of progressive uncoordinated change in head and gait posture. Magnetic resonance imaging (MRI) showed a lesion in posterior cranial fossa characterized by iso- to hypo-intensity in T1 and iso- to hyper-intensity in T2 with a homogeneous contrast uptake. The case received a one-month course of steroid therapy, and then performed by suboccipital craniectomy. The histopathological examination was described as CPC. The neurological symptoms were immediately and significantly improved after surgery. Follow-up MRI demonstrated that approximately 60% of the tumor was resected. To our knowledge, the clinical outcome of CPC was very poor. In this study, we provided an effective surgical approach, suboccipital craniectomy, for CPC in the posterior cranial fossa to avoid excess brain damage.


Author(s):  
Ahmed Reda ◽  
Ihab Gomaa

AbstractThe present study is a case report of vulvar lipoma. The vulva is a rare site for the development of lipomas, and the aim of the study is to determine if the current imaging modalities can diagnose lipomas correctly. A 43-year-old patient presented with a painless, slowly progressive, oval, mobile and non-tender right vulvar mass compressing the vagina and totally covering the introitus. Both the ultrasonography and magnetic resonance imaging (MRI) exams suggested the diagnosis of lipoma. Surgical excision was performed, and the histopathological examination of the mass confirmed a lipoma.


2001 ◽  
Vol 95 (6) ◽  
pp. 1040-1044 ◽  
Author(s):  
Alexis Byrne Carter ◽  
Donald L. Price ◽  
Keith A. Tucci ◽  
Gregory K. Lewis ◽  
Jeffrey Mewborne ◽  
...  

✓ A 6-year-old girl with a history of a nondisplaced skull fracture diagnosed with computerized tomography (CT) scanning 3 years previously presented with a 6-week history of headaches and decreased use of her right side. On admission CT scans, a large cystic mass was identified in the left frontal lobe region of the brain. A connection between the mass and the ventricular system was not seen on radiological examination or during surgery. Gross-total resection of the mass was achieved. The histological and immunohistochemical findings in the resected tissue confirmed a diagnosis of choroid plexus carcinoma (ChPC). This is the first reported case of a ChPC arising in an extraventricular location not associated with the choroid plexus.


2011 ◽  
Vol 22 (2) ◽  
pp. 404-406 ◽  
Author(s):  
Rei Enatsu ◽  
Stephen Hantus ◽  
Jorge Gonzalez-Martinez ◽  
Norman So

2017 ◽  
Vol 1 (2) ◽  
Author(s):  
Azhani C ◽  
Chan KH ◽  
Fadli M ◽  
Saufi A

Author(s):  
Joyce JG ◽  
O’Dowd M ◽  
Ryan RS ◽  
Stokes HS ◽  
ONeill MB

2010 ◽  
Vol 29 (01) ◽  
pp. 14-20 ◽  
Author(s):  
A. Sav ◽  
B.W. Scheithauer ◽  
C.A. Mazzola ◽  
S.R.P. Ketterling ◽  
S.J. Thompson ◽  
...  

2019 ◽  
Vol 21 (Supplement_6) ◽  
pp. vi99-vi99
Author(s):  
Kyu Sang Lee ◽  
Gheeyoung Choe

Abstract Primary glioblastoma develops de novo without clinical or histological evidence of a low-grade precursor lesion, while secondary glioblastoma develops from a low-grade glioma. The same IDH mutation is observed in almost secondary glioblastomas that occurs in low-grade gliomas with IDH mutation. Present report is an extraordinary case of secondary glioblastoma, IDH-wildtype arising in diffuse astrocytoma, IDH-mutant. A 31-year-old female presented with seizure 3 months ago, who had a history of operation for diffuse astrocytoma, IDH-mutant on the left frontal lobe 6 years ago. Magnetic resonance imaging test revealed new infiltrative lesions (6.5cm) in left frontal lobe and corpus callosum, in addition to the non-enhancing mass (3.4cm). New infiltrative lesion suspected anaplastic change and the patient underwent tumorectomy. Microscopically, non-enhancing lesion showed high cellularity, moderate nuclear atypia and brisk mitosis. Microvascular proliferation and necrosis were absent that can be diagnosis as anaplastic astrocytoma. However, new infiltrative lesion showed microvascular proliferation and necrosis that acceptable for diagnosis as glioblastoma. IDH-1 immunohistochemistry (IHC) was positive in anaplastic astrocytoma but negative in glioblastoma. In addition, we assessed NGS based on the SNUBH Brain v1.0 (Macrogen, Seoul, South Korea) panel. Similar to IHC result, IDH-1 (p.Arg132His) mutation was found in anaplastic astrocytoma but not in glioblastoma. Interestingly, ATRX (p.Gln1670Ter) and TP53 (p.His193Arg) mutations were found in both lesions. Additionally, PTEN (p.His296Pro) mutation was identified in glioblastoma component only. Until now, it is well-known hypothesis that the IDH mutation initiated in glial progenitor cell and the other genetic mutations occur sequentially in pathogenesis of secondary glioblastoma. Notably, this is the first case report that other genetic alterations can be initiated before IDH mutation contrary to previous hypothesis. In our case, mutation of ATRX and TP53 might be initiated, and PTEN and IDH-1 mutations were sequentially occurred in glioblastoma and anaplastic astrocytoma, respectively.


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