COPA Syndrome (Ala239Pro) Presenting with Isolated Follicular Bronchiolitis in Early Childhood: Case Report

2021 ◽  
Author(s):  
Pamela Psarianos ◽  
Jennifer Yin Yee Kwan ◽  
Sharon Dell ◽  
Wallace B. Wee ◽  
Katrina Rey-McIntyre ◽  
...  
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Follicular Bronchiolitis ◽  
Copa Syndrome

scholarly journals Dental Treatments under the General Anesthesia in a Child with Keratitis, Ichthyosis, and Deafness Syndrome

2013 ◽  
Vol 2013 ◽  
pp. 1-6
Author(s):  
Sera Sımsek Derelioglu ◽  
Yücel Yılmaz ◽  
Sultan Keles
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
General Anesthesia ◽  
Early Childhood Caries ◽  
Sensorineural Deafness ◽  
Oral Symptoms ◽  
Severe Early Childhood Caries ◽  
Childhood Caries

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.

scholarly journals Oral Angioleiomyoma in Early Childhood Patient: A Case Report of an Uncommon Lesion and Literature Review

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

scholarly journals Early Childhood Caries: A Case Report of an Extensive Rehabilitation

2018 ◽  
Author(s):  
Gabriela Maltz Goldenfum ◽  
Sofia Conte Dallagnol ◽  
Jonas De Almeida Rodrigues
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Early Childhood Caries ◽  
Childhood Caries

scholarly journals A Prolapsed Cecoureterocele in an Adult Treated Conservatively: Highly Rare, but Existent

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Löcherbach Florian ◽  
Preusser Stefan ◽  
Meier Mark
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Urinary Tract ◽  
Surgical Therapy ◽  
Surgical Procedure ◽  
Unusual Case ◽  
Ectopic Ureterocele ◽  
History Of ◽  
Urinary Tract Anomalies

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.

Lumbar disc herniation in early childhood: case report and literature review

2003 ◽  
Vol 19 (4) ◽  
pp. 258-260 ◽  
Author(s):  
Juan F. Martínez-Lage ◽  
Víctor Fernández Cornejo ◽  
Francisco López ◽  
Máximo Poza
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Literature Review ◽  
Lumbar Disc Herniation ◽  
Disc Herniation ◽  
Lumbar Disc

scholarly journals Mediastinal Cystic Teratoma with Right Sided Extra Renal Wilms’ Tumor - A Rare Case Report

2018 ◽  
Vol 42 (3) ◽  
pp. 155-158
Author(s):  
AKMA Morshed ◽  
S Islam ◽  
K Alam
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Germ Cell ◽  
Rare Case ◽  
Wilms Tumor ◽  
Germ Cell Tumors ◽  
Cystic Teratoma ◽  
Cell Tumor ◽  
Mediastinal Teratoma ◽  
Rare Case Report

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

scholarly journals Follicular Bronchiolitis: A Rare Cause of Bronchiolitis Obliterans Syndrome After Lung Transplantation: A Case Report

2009 ◽  
Vol 9 (3) ◽  
pp. 644-650 ◽  
Author(s):  
R. Vos ◽  
B. M. Vanaudenaerde ◽  
S. I. De Vleeschauwer ◽  
D. E. Van Raemdonck ◽  
L. J. Dupont ◽  
...  
Keyword(s):  
Case Report ◽  
Lung Transplantation ◽  
Bronchiolitis Obliterans ◽  
Bronchiolitis Obliterans Syndrome ◽  
Follicular Bronchiolitis

scholarly journals A Case Report of Female Patient with Laryngeal Granuloma

2017 ◽  
Vol 18 (2) ◽  
pp. 175-177
Author(s):  
Sladjana Simovic ◽  
Tatjana Sarenac Vulovic ◽  
Jasmina Stojanovic ◽  
Sandra Zivanovic ◽  
Mladen Koravovic
Keyword(s):  
Early Childhood ◽  
Case Report ◽  
Tracheal Intubation ◽  
General Anesthesia ◽  
Female Patient ◽  
Direct Laryngoscopy ◽  
Potential Complication ◽  
Patient Case ◽  
Vocal Cords ◽  
Laryngeal Granuloma

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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