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A rare case of pulmonary malignant peripheral nerve sheath tumor. 2023

Rita Costa, and José Maximo, and Pedro Fernandes, and Susana Guimarães, and Roberto Silva, and Adriana Magalhães
Department of Cardiothoracic Surgery, Centro Hospitalar Universitário são João, Portugal. Electronic address: rita2ac@hotmail.com.

UI MeSH Term Description Entries
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D018319 Neurofibrosarcoma A malignant tumor that arises from small cutaneous nerves, is locally aggressive, and has a potential for metastasis. Characteristic histopathologic features include proliferating atypical spindle cells with slender wavy and pointed nuclei, hypocellular areas, and areas featuring organized whorls of fibroblastic proliferation. The most common primary sites are the extremities, retroperitoneum, and trunk. These tumors tend to present in childhood, often in association with NEUROFIBROMATOSIS 1. (From DeVita et al., Cancer: Principles & Practice of Oncology, 5th ed, p1662; Mayo Clin Proc 1990 Feb;65(2):164-72) Malignant Peripheral Nerve Sheath Tumors,Neurilemmosarcoma,Sarcoma, Neurogenic,MPNST,Malignant Neurilemmoma,Malignant Neurilemoma,Malignant Peripheral Nerve Sheath Tumor,Peripheral Nerve Sheath Tumors, Malignant,Schwannoma, Malignant,Malignant Neurilemmomas,Malignant Neurilemomas,Malignant Schwannoma,Malignant Schwannomas,Neurilemmoma, Malignant,Neurilemmosarcomas,Neurilemoma, Malignant,Neurofibrosarcomas,Neurogenic Sarcoma,Neurogenic Sarcomas,Sarcomas, Neurogenic

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