Primitive neuroectodermal tumor originating from the lung: A case report

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Primitive neuroectodermal tumor originating from the lung: A case report.

Primitive neuroectodermal tumors (PNETs) are small, round cell tumors that may be classified as peripheral or central, based on their site of origin. PNETs often arise in the soft tissue or bone of young adults. Although not common, PNETs have been described in other organs, including the gonads, kidneys, myocardium and pancreas, but rarely in the lungs without chest wall or pleural involvement...

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Primitive neuroectodermal tumor originating in the vulva: A case report

Primitive neuroectodermal tumors (PNETs) exhibit chromosomal translocations in common with those of Ewing's sarcoma. They usually originate in bone or soft tissue but rarely arise in the vulva. The current case report presents a case of PNET originating in the vulva in a 60-year-old female, who previously underwent enucleation of a vulvar tumor in another hospital. The pathologist suspected a h...

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[Pancreatic primitive neuroectodermal tumor: case report].

Primitive neuroectodermal tumors (PNETs) are small round cell malignant tumors classified as part of the Ewing’s sarcoma family of neoplasms, which represents approximately 1% of all sarcomas1. Predominantly occurring in soft tissues along the extremities, they have also been reported in a variety of organs such as kidney, urinary bladder, testis, ovary, uterus, heart and lung2, 3. Pancreatic P...

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Peripheral Primitive Neuroectodermal Tumor of the Pelvis

The primitive neuroectodermal tumor (PNET) belongs to a group of highly malignant tumors and is composed of small round cells of a neuroectodermal origin. Categorized in the same tumor family as Ewing sarcoma, the PNET is most likely to occur in bones and soft tissues. However, a small number of PNET cases arising in the pelvis have been reported as well. We present three cases of pelvic PNET: ...

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primitive neuroectodermal tumor with kidney involvement: a case report

primitive neuroectodermal tumor (pnet) is usually an aggressive, rapidly progressing and metastasizing tumor. occurrence of this type of tumor in the kidney is considered as unusual and few cases have been reported so far. we present a metastatic pnet arising probably from the kidney in a 17-year-old female patient with local invasion and metastasis to the stomach. pnet should be considered as ...

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ژورنال

عنوان ژورنال: Oncology Letters

سال: 2016

ISSN: 1792-1074,1792-1082

DOI: 10.3892/ol.2016.4973