Infantile and Congenital Tumor

2019 ◽  
pp. 1-20
Author(s):  
Federico Bianchi ◽  
Gianpiero Tamburrini
Keyword(s):  
Congenital Tumor

Infantile and Congenital Tumor

2020 ◽  
pp. 1835-1851
Author(s):  
Federico Bianchi ◽  
Gianpiero Tamburrini
Keyword(s):  
Congenital Tumor

scholarly journals Choristoma: A rare congenital tumor of the tongue

2016 ◽  
Vol 6 (2) ◽  
pp. 311 ◽  
Author(s):  
JessicaPatricia Correa Jorquera ◽  
Josep Rubio-Palau ◽  
AsteriaAlbert Cazalla ◽  
Leonardo Rodríguez-Carunchio
Keyword(s):  
Congenital Tumor

scholarly journals Congenital unilateral ocular fibrosis syndrome secondary to benign congenital tumor

2006 ◽  
Vol 54 (2) ◽  
pp. 123 ◽  
Author(s):  
P Vijayalakshmi ◽  
Jitendra Jethani ◽  
Usha Kim
Keyword(s):  
Congenital Tumor

Congenital tumor of atrioventricular node with complete heart block and sudden death

1972 ◽  
Vol 29 (4) ◽  
pp. 554-557 ◽  
Author(s):  
Larry V. Lewman ◽  
Martial A. Demany ◽  
Henry A. Zimmerman
Keyword(s):  
Sudden Death ◽  
Heart Block ◽  
Complete Heart Block ◽  
Atrioventricular Node ◽  
Congenital Tumor

Congenital Tumor With a Vascular Appearance

2008 ◽  
Vol 99 (4) ◽  
pp. 305-306
Author(s):  
I. Cervigón ◽  
L.M. Torres ◽  
Á. Palomo
Keyword(s):  
Congenital Tumor

scholarly journals Dermoid cyst of the anterior fontanelle in adults: case report

2007 ◽  
Vol 65 (1) ◽  
pp. 170-172 ◽  
Author(s):  
Ricardo Antônio Gênova de Castro ◽  
Afonso de Souza Ribeiro Filho ◽  
Valderi Vieira da Silva Jr.
Keyword(s):  
Case Report ◽  
Head And Neck ◽  
Dermoid Cyst ◽  
Surgical Intervention ◽  
Histopathological Examination ◽  
Anterior Fontanelle ◽  
Congenital Tumor

Head and neck dermoid cysts are lesions relatively rare, which usually occur during childhood as solitary lesions. They are often identified and surgically removed at birth, being uncommon in adults. A 23-year-old male presented with a congenital tumor of the anterior fontanelle, which histopathological examination revealed a dermoid cyst. Surgical intervention is the treatment of choice to remove this lesion. The objective of this study is to report the case, once this type of lesion is rare in adults.

Congenital Tumor of the Hand and Upper Limb

2017 ◽  
pp. 445-470
Author(s):  
Jinghong Xu ◽  
Jialiang Chen ◽  
Qifang He ◽  
Liulong Zhu ◽  
Jianmin Yao
Keyword(s):  
Upper Limb ◽  
Congenital Tumor

Intraocular Medulloepithelioma

2012 ◽  
Vol 136 (2) ◽  
pp. 212-216 ◽  
Author(s):  
Timothy Saunders ◽  
Curtis E. Margo
Keyword(s):  
Fine Needle Aspiration Biopsy ◽  
Needle Aspiration ◽  
Good Prognosis ◽  
Definitive Diagnosis ◽  
Ciliary Epithelium ◽  
Histologic Diagnosis ◽  
Fine Needle ◽  
Congenital Tumor ◽  
Mesenchymal Tissue ◽  
The Central Nervous System

Intraocular medulloepithelioma is a congenital tumor of the ciliary epithelium that typically presents during the first decade of life. The histologic diagnosis is based on characteristic ribbons of pseudostratified neuroepithelium admixed with loose mesenchymal tissue rich in hyaluronic acid, vaguely resembling developing retina and vitreous. More than a third of medulloepitheliomas contain heteroplastic tissue, which in some cases makes up most of the tumor. Malignant medulloepitheliomas consist of a proliferation of neuroblasts, which in areas can be indistinguishable from retinoblastoma. Unlike its highly malignant counterpart in the central nervous system, intraocular medulloepithelioma has a good prognosis as long as tumor has not spread beyond the eye. Definitive diagnosis and eye-conserving therapy is possible with fine-needle aspiration biopsy. The histologic differential diagnosis of medulloepithelioma is broad, ranging from retinoblastoma and sarcoma to ciliary epithelial adenoma and adenocarcinoma.

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