Germinoma of the Mediastinum: A Case Report with Special Reference to the Histogenesis of Mediastinal Teratoma

1959 ◽  
Vol 36 (4) ◽  
pp. 438-441 ◽  
Author(s):  
KIYOSHI INADA ◽  
AKINORI NAKANO
2007 ◽  
Vol 56 (1) ◽  
pp. 51
Author(s):  
Jinoo Kim ◽  
Yo Won Choi ◽  
Seok Chol Jeon ◽  
Jeong Nam Heo ◽  
Choong-Ki Park ◽  
...  

2019 ◽  
Vol 47 (6) ◽  
pp. 380-383
Author(s):  
Li Xiao‐dong ◽  
Zhang Li ◽  
Duan Xiu‐mei ◽  
Tang Ming‐bo ◽  
Wang Xiao‐cong

2021 ◽  
Vol 80 ◽  
pp. 105680
Author(s):  
Maciej Rachwalik ◽  
Kinga Kosiorowska ◽  
Maciej Bochenek ◽  
Marek Jasinski ◽  
Roman Przybylski

1988 ◽  
Vol 8 (4) ◽  
pp. 283-290 ◽  
Author(s):  
Yasuo Ooe ◽  
Motoichirou Katoh ◽  
Haruo Kashima ◽  
Takashi Handa ◽  
Hatsu Tsuruoka

2017 ◽  
Vol 02 (03) ◽  
Author(s):  
Mohammad Serajus Salekin ◽  
Mohammad Tajul Islam

2015 ◽  
Vol 5 (4) ◽  
pp. 213
Author(s):  
Pankaj Srivastava ◽  
ManojKumar Srivastava ◽  
Shalini Srivastava ◽  
Sandeep Roshan

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


2020 ◽  
Vol 15 (10) ◽  
pp. 1870-1874
Author(s):  
Kazuhiko Morikawa ◽  
Satoshi Tatsuno ◽  
Shigeki Misumi

1996 ◽  
Vol 75 (10) ◽  
pp. 658-668 ◽  
Author(s):  
Yousry El-Sayed ◽  
Hamad Al-Muhaimeed

Although laryngeal stenosis caused by cicatricial pemphigoid (CP) is a well documented entity, reports about its surgical treatment are scant. This may be due to the reluctance of the surgeons to excise the scarring, knowing the recurrent nature of the disease. In this paper we report a case of severe laryngeal stenosis caused by CP which necessitated a tracheostomy. When the disease had stabilized, laryngeal airway was restored following open surgical excision and stenting. The historic, clinical, histologic, immunopathologic and therapeutic features of CP are presented with special reference to the laryngeal lesions.


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