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1.
J Assoc Physicians India ; 64(3): 82-85, 2016 03.
Artigo em Inglês | MEDLINE | ID: mdl-27731566

RESUMO

A young male labourer developed pain at the site of blunt trauma over back of chest followed by fever, cough with expectoration, breathlessness and hemorrhagic pleural effusion in the side of injury. What could have been passed as a sequel of trauma turned out to be the consequences of an underlying rare and aggressive malignant tumor of the chest wall known as Askin tumor or Primitive Neuroectodermal Tumor (PNET). CT thorax with guided FNAC, debulking operation, histopathological examination followed by immunohistochemistry of the tumor tissue led to the final diagnosis. Chemotherapy was administered following surgical resection. The patient died within nine months after diagnosis.


Assuntos
Neoplasias Ósseas/diagnóstico por imagem , Neoplasias Ósseas/patologia , Tumores Neuroectodérmicos Primitivos/diagnóstico por imagem , Tumores Neuroectodérmicos Primitivos/patologia , Sarcoma de Ewing/diagnóstico por imagem , Sarcoma de Ewing/patologia , Neoplasias Torácicas/diagnóstico por imagem , Neoplasias Torácicas/patologia , Biomarcadores Tumorais , Biópsia , Neoplasias Ósseas/terapia , Ciclofosfamida/administração & dosagem , Ciclofosfamida/uso terapêutico , Procedimentos Cirúrgicos de Citorredução , Doxorrubicina/administração & dosagem , Doxorrubicina/uso terapêutico , Humanos , Imuno-Histoquímica , Masculino , Tumores Neuroectodérmicos Primitivos/terapia , Derrame Pleural , Sarcoma de Ewing/terapia , Neoplasias Torácicas/terapia , Tomografia Computadorizada por Raios X , Vincristina/administração & dosagem , Vincristina/uso terapêutico , Adulto Jovem
2.
Ann Indian Acad Neurol ; 15(1): 51-3, 2012 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-22412275

RESUMO

Neurofibromatosis 1 (NF1) is the most common neurocutaneous syndrome. It is estimated to occur in approximately 1 out of every 3300 infants. The manifestations of this condition are diverse and can arise from almost any system in the body. The neurofibroma is the hallmark lesion of NF1 that develops from peripheral nerves. Here, we are reporting an 18-year-old girl with NF1. Clinical diagnosis was made according to the diagnostic criteria established by the National Institutes of Health Consensus Development Conference in 1987. She presented with quadriparesis due to dumbbell-shaped spinal schwannoma in the cervical region. She had history of recurrent seizures in the past, with poor scholastic performance. There were clinical and electrophysiological features of peripheral neuropathy and clinical and echocardiographical features of pulmonary stenosis. These are uncommon features of NF 1. The presence of all these features in a single patient makes it a unique case.

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