scholarly journals An unexpected sudden death due to a choroid plexus papilloma: an autopsy case report

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mohamed Amine Zaara ◽  
Sarra Gharsallaoui ◽  
Nihed Abdessayed ◽  
Sarra Mestiri ◽  
Dorra Chiba ◽  
...  

Abstract Background Choroid plexus papillomas (CPPs) are histopathologically benign and rare central nervous system tumors. These tumors remain more frequent in children than adults. It is infrequent for these tumors to cause a sudden unexpected death. We aim in this case to discuss the unusual and fatal presentation of choroid plexus papilloma and the mechanism of death. Case presentation we report the case of a 61-year-old man with no medical history, diagnosed at autopsy with a previously unknown CPP. Initial complaints were chronic headache occurring in the last month and acute chest pain for two days. The forensic autopsy including the histopathologic examination showed a tumoral mass of the choroid plexus in the fourth ventricle diagnosed as a psammomatous CPP. The cause of death in this case was attributed to a massive cerebral edema caused by the tumoral mass. Conclusions Through this case report, we stress the importance of an early and a vigorous investigation of every headache and an early detection of this tumor and we highlight as well the role of the post mortem examination to detect such a fatal complication.

1994 ◽  
Vol 30 (4) ◽  
pp. 643
Author(s):  
Joo Hyeong Oh ◽  
Tae Hoon Kim ◽  
Woo Suk Choi

2015 ◽  
Vol 32 (4) ◽  
pp. 717-721 ◽  
Author(s):  
Gustavo S. Jung ◽  
Leonardo G. Ruschel ◽  
Andre G. Leal ◽  
Ricardo Ramina

1990 ◽  
pp. 144-145
Author(s):  
Yoshihiko Yoshii ◽  
Junichi Tosa ◽  
Shingo Takano ◽  
Shizuo Shirai ◽  
Tetsuo Owada ◽  
...  

Author(s):  
Maria Santos ◽  
Eric Bouffet ◽  
Carolyn Freeman ◽  
Mark M. Souweidane

Choroid plexus tumours are rare, intraventricular, primary central nervous system tumours derived from the choroid plexus epithelium. They occur predominantly in children and are classified based on histological criteria as choroid plexus papilloma, atypical choroid plexus papilloma, and choroid plexus carcinoma. Choroid plexus carcinomas can occur in the context of Li–Fraumeni syndrome, where the TP53 germline mutation predisposes patients to a wide range of neoplasms. Treatment of these tumours is challenging, due to their high vascularity and the young age of the patients. While surgery is the mainstay of treatment of all choroid plexus tumours, the exact role of adjuvant therapy, particularly in choroid plexus carcinoma, is still unclear. For incompletely resected tumours, there is evidence that neoadjuvant chemotherapy can facilitate second-look surgery and reduce the risk of intraoperative bleeding. However, the role of adjuvant radiation after complete resection remains unclear.


2017 ◽  
Vol 105 ◽  
pp. 1039.e13-1039.e18 ◽  
Author(s):  
Xuan Gong ◽  
Chao Liu ◽  
Longbo Zhang ◽  
Zhenyan Li ◽  
Christopher M. Bartley ◽  
...  

2017 ◽  
Vol 6 (14) ◽  
pp. 1153-1155
Author(s):  
Jini Lonappan Valooran ◽  
Anand T P ◽  
Noushad A ◽  
Joy Augustine

2016 ◽  
Vol 3 (87) ◽  
pp. 4777-4778
Author(s):  
Ezhil Arasi Nagamuthu ◽  
Anunayi J ◽  
Syeda Iffath Tahseen

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