Results 101 to 110 of about 1,141 (148)
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Sacral Neurofibrosarcoma — A Case Report
Journal of Medical Imaging and Radiation Oncology, 1986ABSTRACTNeurofibrosarcoma is a rare tumour. A case of sacral neurofibrosarcoma is presented. The role of computed tomography in defining this lesion is discussed.
M R Sage
exaly +3 more sources
Neurofibrosarcoma of the duodenum
European Journal of Surgical Oncology (EJSO), 1995A case of neurofibrosarcoma of the second part of the duodenum is reported. The presenting symptom was upper GI tract bleeding. An emergency pancreaticoduodenectomy was performed to remove a 6 x 8 cm tumour invading the head of the pancreas and the ampulla of Vater.
J, Melissas +4 more
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Journal of Pediatric Surgery, 2003
Neurofibrosarcoma is rare in children, and the natural history and prognostic factors are not well described. The authors present a 57-year review of their experience.The charts of children with neurofibrosarcoma were reviewed retrospectively. Statistical analysis was performed using the Chi2 and unpaired t tests.From 1944 to 2001, 38 patients under ...
Holly, Neville +3 more
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Neurofibrosarcoma is rare in children, and the natural history and prognostic factors are not well described. The authors present a 57-year review of their experience.The charts of children with neurofibrosarcoma were reviewed retrospectively. Statistical analysis was performed using the Chi2 and unpaired t tests.From 1944 to 2001, 38 patients under ...
Holly, Neville +3 more
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The Annals of Thoracic Surgery, 1991
A 56-year-old woman was seen with the clinical features of collapse of the right lower lobe. Intrabronchial extension of a tumor was demonstrated endoscopically. Sleeve bilobectomy was performed, and a diagnosis of bronchial neurofibrosarcoma was confirmed by light and electron microscopic and immunohistochemical studies.
K, Kodama +4 more
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A 56-year-old woman was seen with the clinical features of collapse of the right lower lobe. Intrabronchial extension of a tumor was demonstrated endoscopically. Sleeve bilobectomy was performed, and a diagnosis of bronchial neurofibrosarcoma was confirmed by light and electron microscopic and immunohistochemical studies.
K, Kodama +4 more
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Malignant Spinal Neurofibrosarcoma
Spine, 2000A report of a case of metastatic spinal neurofibrosarcoma.To document metastatic neurofibrosarcoma as a cause of spinal cord compression and to review the literature.Three previously reported cases of metastatic neurofibrosarcoma of the spine were reviewed.The patient's clinical record and radiologic investigations as well as the result of a search of ...
R, Kett-White +3 more
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Neurofibrosarcoma complicating pregnancy
Gynecologic Oncology, 1989Sarcomatous degeneration of a neurofibroma during pregnancy is exceedingly rare. Prompt diagnosis followed by surgical resection is recommended.
V V, Baker, K D, Hatch, H M, Shingleton
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Seriously saRComa: Neurofibrosarcoma
European Journal of Dermatology, 2016A 24-year-old male presented with a subcutaneous tumour measuring approximately 10 cm in diameter on his left thigh. The tumour appeared firm on palpation and did not show epidermal alterations (figure 1A). The patient reported that the lesion had been slowly growing in size over a period of a few months.
Valeria, Behle +2 more
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Retroperitoneal pelvic neurofibrosarcoma
The American Journal of Surgery, 1960Abstract Retroperitoneal pelvic neurofibrosarcoma is a rare tumor, and taking pathologic synonyms into account, only six cases could be found in the literature. The patient herein discussed presented with a cutaneous neurofibroma, and after its removal evidence of involvement of the pelvic nerve trunk appeared.
D, CAVANAGH, F, ALONOSO-LEJ
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Neurofibrosarcomas of the upper extremity
The Journal of Hand Surgery, 1991A retrospective review of all malignant hand tumors seen at the University of Michigan from 1950 to 1987 demonstrated six biopsy-proven cases of neurofibrosarcoma involving the upper extremity. There were four male and two female patients; average age at presentation was 37 years and ages ranged from 15 to 63 years.
R P, Rogalski, D S, Louis
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Digital neurofibrosarcoma in infancy
The Journal of Pediatrics, 1957Summary 1. Neurofibrosarcoma of the digits in infants, though rare, presents a distinct clinical picture. 2. Our experience with six cases is presented. 3. The multicentric origin is suggestive of an infectious (? virus) etiology of this malignant tumor. 4.
A R, JENSEN, L W, MARTIN, L A, LONGINO
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