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1.
Head Face Med ; 9: 35, 2013 Nov 25.
Artigo em Inglês | MEDLINE | ID: mdl-24274360

RESUMO

Melanotic neuroectodermal tumor of infancy (MNTI) is a rare condition that occurs normally in the anterior maxilla of infants aged <1 year. The use of clinical and imaging tools for MNTI is extremely important to prevent problems with function as well as the aesthetic features in a breastfeeding child. Brazil is a multiethnic country with a poor epidemiological policy and little data to track the incidence of certain diseases, including MNTI. It is important to study this pathology with ethnicity as a factor to improve the current epidemiological programs and establish better post-treatment management. This paper describes a case of a 2-month-old male of African-indigenous descent and Brazilian Amazon residency, who presented to our unit in 2009 with a history of an expanding mass involving the anterior maxilla. Clinical and computerized tomography scans were used to diagnose the mass as MNTI, which was removed by total excision. A biopsy later confirmed the MNTI diagnosis.


Assuntos
População Negra , Indígenas Sul-Americanos , Neoplasias Maxilares/diagnóstico , Neoplasias Maxilares/etnologia , Tumor Neuroectodérmico Melanótico/diagnóstico , Tumor Neuroectodérmico Melanótico/etnologia , Brasil/epidemiologia , Humanos , Lactente , Masculino , Neoplasias Maxilares/diagnóstico por imagem , Neoplasias Maxilares/cirurgia , Tumor Neuroectodérmico Melanótico/diagnóstico por imagem , Tumor Neuroectodérmico Melanótico/cirurgia , Procedimentos Cirúrgicos Bucais , Tomografia Computadorizada por Raios X
2.
Med Oral Patol Oral Cir Bucal ; 11(2): E112-4, 2006 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-16505785

RESUMO

Progressive Hemifacial Atrophy, also known as Parry-Romberg Syndrome, is an uncommon degenerative and poorly understood condition. It is characterized by a slow and progressive atrophy affecting one side of the face. The incidence and the cause of this alteration is unknown. A cerebral disturbance of fat metabolism has been proposed as a primary cause. This can be the result of a trophic malformation of Cervical Sympathetic Nervous System. Possible factors that are involved in the pathogenesis include trauma, viral infections, heredity, endocrine disturbances and auto-immunity, among others. The most common complications that appear in association to this health disorder are: trigeminal neuritis, facial paresthesia, severe headache and epilepsy, being this last one the most frequent complication of the Central Nervous System. Characteristically, the atrophy progresses slowly for several years and, soon after, it become stable. Now, plastic surgery with graft of autogenous fat can be performed, after stabilization of the disease, to correct the deformity. Orthodontic treatment can help in the correction of any associated malformation. The objective of this work is, through the presentation of a clinical case, to accomplish a literature review concerning general characteristics, etiology, physiopathology, differential diagnosis and treatment of progressive hemifacial atrophy.


Assuntos
Hemiatrofia Facial , Criança , Progressão da Doença , Hemiatrofia Facial/diagnóstico , Hemiatrofia Facial/etiologia , Hemiatrofia Facial/fisiopatologia , Hemiatrofia Facial/terapia , Feminino , Humanos
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