scholarly journals Duodenal teratoma: Rare case of extragonadal germ cell tumors and review of literature

2021 ◽  
Vol 86 ◽  
pp. 106377
Author(s):  
Bilal Chamaa ◽  
Jad Terro ◽  
Mostapha Mneimneh ◽  
Sirage Edris ◽  
Etienne El-Helou
2016 ◽  
Vol 2016 ◽  
pp. 1-4 ◽  
Author(s):  
Sammy G. Nakhla ◽  
Srinath Sundararajan

Mediastinal germ cell tumors are extragonadal germ cell tumors (EGGCTs) commonly seen in children and young adults. They are more common in men. Clinically they are classified as teratomas, seminomas, and nonseminomatous germ cell tumors. Primary mediastinal yolk sac neoplasm is an extremely rare tumor. We present here a very rare case of primary yolk sac tumor of the anterior mediastinum in a 73-year-old male. Mediastinal germ cell tumors have a worse prognosis than gonadal germ cell tumors. Chemotherapy followed by adjuvant surgery improves overall response in EGGCTs. However, comorbidities can render treatment with chemotherapy and surgery challenging in elderly patients.


2020 ◽  
Vol 22 (Supplement_3) ◽  
pp. iii329-iii329
Author(s):  
Hiroki Yamada ◽  
Tomohiro Abiko ◽  
Hirokazu Fujiwara ◽  
Kazunari Yoshida ◽  
Hikaru Sasaki

Abstract INTRODUCTION Germ cell tumors in the central nervous system (CNS) typically arise either at suprasellar and/or pineal region, and occasionally at basal ganglia. We report a case of diagnostically challenging, recurrent germ cell tumor presented with diffuse intraaxial abnormality in and across the lower brainstem, which was diagnosed by the elevated placental alkaline phosphatase (PLAP) level in cerebrospinal fluid (CSF). CASE DESCRIPTION: A 28-year-old man had been treated by chemoradiotherapy at the previous hospital for bifocal suprasellar and pineal lesions with the provisional diagnosis of germinoma without histological confirmation. Three years later, he presented with progressive weakness of bilateral extremities for weeks. Magnetic resonance imaging showed a diffuse, bilaterally symmetric high intensity lesion on T2-weighted image with slight contrast enhancement across the ventral side of the medulla oblongata to the upper cervical spinal cord. Serum and CSF hCG, hCG-β, and AFP were all negative. Since the image findings were atypical for recurrent germ cell tumor, some kind of myelitis was initially suspected. Therefore, steroid pulse therapy was administered. However, the patient’s symptom was still gradually progressing. Then, the CSF PLAP turned out to be positive, indicating the recurrence of germinoma. Accordingly, platinum-based chemotherapy was administered, and the imaging findings, patient’s symptoms, and CSF PLAP began to improve. The patient is to be treated with radiotherapy following chemotherapy. CONCLUSION We report a rare case of CNS germ cell tumor that presented with diffuse intraaxial lesion in the lower brainstem in which examination of CSF PLAP was extremely useful.


Cancer ◽  
2012 ◽  
Vol 118 (17) ◽  
pp. 4290-4297 ◽  
Author(s):  
Ramandeep S. Arora ◽  
Robert D. Alston ◽  
Tim O. B. Eden ◽  
Marco Geraci ◽  
Jillian M Birch

1992 ◽  
Vol 3 (4) ◽  
pp. 283-289 ◽  
Author(s):  
G. Daugaard ◽  
M. Rørth ◽  
H. von der Maase ◽  
M. Skakkebæk

2020 ◽  
Vol 27 (1) ◽  
pp. 61-66
Author(s):  
Yura Kim ◽  
Won Kee Ahn ◽  
Jung Woo Han ◽  
Seung Min Hahn ◽  
Seung Yeon Kwon ◽  
...  

1994 ◽  
Vol 1 (2) ◽  
pp. 172-176 ◽  
Author(s):  
Mutsushi Kawakita ◽  
Toshiro Terachi ◽  
Shuichi Hida ◽  
Hideo Takeuchi ◽  
Osamu Yoshida

2012 ◽  
Vol 17 (1) ◽  
pp. 9
Author(s):  
Kanishka Das ◽  
Mainak Deb ◽  
Suravi Mohanty ◽  
Anuradha Ananthamurthy ◽  
Isha Garg

2018 ◽  
Vol 42 (3) ◽  
pp. 155-158
Author(s):  
AKMA Morshed ◽  
S Islam ◽  
K Alam

A teratoma of the mediastinum is an uncommon germ cell tumor. Five percent of germ cell tumors are extragonadally located and men are affected more than women .Most mediastinal teratoma produce no symptoms, but we are presenting a case which was present with respiratory distress in early childhood. Classical wilm’s tumor usually found within the kidney but rarely it can occur in extra renal situations. Combination of these two is not reported until today we have searched extensively. We are presenting a 26 month old boy with mediastinal cystic teratoma with right sided extra renal wilms’ tumor which may be the first reported case. Combined effort of various concern departments ensures the diagnosis and management of such a rare case. Bangladesh J Child Health 2018; VOL 42 (3) :155-158


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