scholarly journals Multifocal pheochromocytoma in early childhood: case report

2011 ◽  
Vol 87 (6) ◽  
Author(s):  
C Yuko-Jowi ◽  
R Mukhwana ◽  
FE Onyango
Keyword(s):  
Author(s):  
Pamela Psarianos ◽  
Jennifer Yin Yee Kwan ◽  
Sharon Dell ◽  
Wallace B. Wee ◽  
Katrina Rey-McIntyre ◽  
...  

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Sera Sımsek Derelioglu ◽  
Yücel Yılmaz ◽  
Sultan Keles

KID syndrome is a rare genodermatosis characterized by keratitis, ichthyosis, and sensorineural deafness. Although the dermatological, ophthalmologic, and sensorineural defects are emphasized in the literature, oral and dental evaluations are so superficial. In this case report, dental and oral symptoms of a three year and five months old boy with KID syndrome, suffering severe Early Childhood Caries (s-ECC) and dental treatments done under General Anesthesia (GA) were reported.


2021 ◽  
Vol 14 (6) ◽  
pp. 828-832
Author(s):  
Francisco SR Carvalho ◽  
Fábio WG Costa ◽  
Thâmara MM Bezerra ◽  
Filipe N Chaves ◽  
Ana PNN Alves ◽  
...  

Author(s):  
Gabriela Maltz Goldenfum ◽  
Sofia Conte Dallagnol ◽  
Jonas De Almeida Rodrigues

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Löcherbach Florian ◽  
Preusser Stefan ◽  
Meier Mark

Ectopic ureteroceles are one of the most common human urinary tract anomalies. They tend to be recognized and treated in early childhood, especially when they have prolapsed. In most cases surgical therapy is inevitable. In this case report, however, we present the unusual case of a 26-year-old woman suffering from a prolapsed cecoureterocele without any known history of an ectopic ureterocele so far. She was successfully treated without the need for a surgical procedure.


2003 ◽  
Vol 19 (4) ◽  
pp. 258-260 ◽  
Author(s):  
Juan F. Martínez-Lage ◽  
Víctor Fernández Cornejo ◽  
Francisco López ◽  
Máximo Poza

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


2017 ◽  
Vol 18 (2) ◽  
pp. 175-177
Author(s):  
Sladjana Simovic ◽  
Tatjana Sarenac Vulovic ◽  
Jasmina Stojanovic ◽  
Sandra Zivanovic ◽  
Mladen Koravovic

AbstractThe aim of this case report is to present the laryngeal granuloma in 23 year old female patient. Case outline: The 23 year old female was admitted for examination, because of long lasting, progressive hoarseness. In anamnesis, we found that she has undergone general anesthesia for 8 times, in the early childhood. We performing direct laryngoscopy with complete otorhinolaryngologic examination, rigid endovideostroboscopy and the large granuloma of the larynx was found. Conclusions: Laryngeal granuloma of vocal cords affected mainly men, except for cases associated with laryngeal intubation. We should keep in mind that postintubation laryngeal granuloma might develop after tracheal intubation, so care must be taken to avoid the potential complication.


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