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1.
J Med Life ; 8(1): 44-8, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-25914738

RESUMO

RATIONALE: Infantile Hemangiomas (IH) are the most frequent tumors of vascular origin, and the differential diagnosis from vascular malformations is difficult to establish. Specific types of IH due to the location, dimensions and fast evolution, can determine important functional and esthetic sequels. To avoid these unfortunate consequences it is necessary to establish the exact appropriate moment to begin the treatment and decide which the most adequate therapeutic procedure is. OBJECTIVE: Based on clinical data collected by a serial clinical observations correlated with imaging data, and processed by a computer-aided diagnosis system (CAD), the study intended to develop a treatment algorithm to accurately predict the best final results, from the esthetical and functional point of view, for a certain type of lesion. METHODS AND RESULTS: The preliminary database was composed of 75 patients divided into 4 groups according to the treatment management they received: medical therapy, sclerotherapy, surgical excision and no treatment. The serial clinical observation was performed each month and all the data was processed by using CAD. DISCUSSIONS: The project goal was to create a software that incorporated advanced methods to accurately measure the specific IH lesions, integrated medical information, statistical methods and computational methods to correlate this information with that obtained from the processing of images. Based on these correlations, a prediction mechanism of the evolution of hemangioma, which helped determine the best method of therapeutic intervention to minimize further complications, was established.


Assuntos
Processamento de Imagem Assistida por Computador , Software , Estatística como Assunto , Neoplasias Vasculares/diagnóstico , Neoplasias Vasculares/terapia , Distribuição por Idade , Diagnóstico Diferencial , Feminino , Hemangioma/diagnóstico , Hemangioma/terapia , Humanos , Masculino
2.
J Med Life ; 7(4): 563-6, 2014.
Artigo em Inglês | MEDLINE | ID: mdl-25713623

RESUMO

RATIONALE: Proteus Syndrome (PS) is an extremely rare congenital pathology that causes overgrowth of multiple tissues, in particular bone and fat, following a mosaic pattern. The estimated incidence is of less than 1 per 1,000.000 live births and represents a significant challenge to the pediatric and orthopedic surgeons in order to establish a diagnosis and to elaborate a management plan. OBJECTIVES: We had the opportunity of treating many children who were afflicted by overgrowth syndromes and have been previously misdiagnosed as Proteus Syndrome in our department of pediatric and orthopedic surgery of "Maria Sklodowska Curie" Clinical Emergency Hospital for Children. This study helped us develop a diagnostic for these patients and report the first case of a confirmed PS in Romania. METHODS AND RESULTS: We report the case of a 5-year-old white male who is in the attention of the clinic since birth. He presented with multiple overgrowth bone segments, fatty subcutaneous or intraabdominal tumors and other connective tissues abnormalities. All the tests performed confirmed the diagnosis of PS at the age of 4 and the management is still to be decided. DISCUSSIONS: We followed the latest diagnostic indications and the patient fulfilled the general and specific criteria. The treatment is still in progress and it represents a challenge for the multidisciplinary medical team.


Assuntos
Síndrome de Proteu/diagnóstico , Síndrome de Proteu/terapia , Pré-Escolar , Humanos , Lactente , Recém-Nascido , Deformidades Congênitas das Extremidades Inferiores/patologia , Linfangioma/cirurgia , Masculino , Nevo/patologia
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