Results 51 to 60 of about 2,464 (251)
Cancer Medicine, Volume 15, Issue 2, February 2026.Encouraging survival is achieved in phakomatosis syndromes with conventional multimodality treatment (Surgery, RT, chemotherapy). There is an urgent need for easily administered systemic therapies which improve both quality and quantity of life. ABSTRACT Purpose Phakomatoses‐associated primary central nervous system (CNS) tumors are therapeutically ...
Anuradha Krishnan +10 more
wiley +1 more source
Ancient schwannoma arising from mental nerve : a case report and review [PDF]
, 2009 Schwannoma is an intraoral rare, benign neoplasm derived from the nerve sheath of peripheral nerves. ?Ancient schwannoma? shows histopathological features, such as degenerative changes and atypical nuclei, and may easily be confused with malignant ...
Balanand, Subramanian +2 more
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Clinical Case Reports, Volume 14, Issue 2, February 2026.Intraoperative photograph showing the reflection of full thickness flap over the body of mandible exposing the lesion and specimen following excisional biopsy. ABSTRACT In the differential diagnosis of nerve‐related lesions, even when there is no documented trauma, this case emphasizes the significance of taking traumatic neuroma into account.
Shristi Maharjan +7 more
wiley +1 more source
Intranodal palisaded myofibroblastoma (intranodal hemorrhagic spindle cell tumor with amianthoid fibers): a case report and literature review [PDF]
, 2010 Intranodal palisaded myofibroblastoma (IPM) is a benign mesenchymal neoplasm originating from smooth muscle cells and myofibroblasts. It is characterized by spindle cells, amianthoid fibers, and by the proliferation of hemosiderin-containing histiocytes ...
Figen Barut +4 more
core +2 more sources
Benign solitary schwannomas (neurilemomas) [PDF]
Cancer, 1969 Three hundred and three patients with benign solitary neurilemomas, or schwannomas, not associated with the classical type of von Recklinghausen's disease were studied. One hundred and seventy-two were women and 131 were men. Forty-five percent of the tumors were seen in the extremities, and no specific area could be related to the development of these
T K, Das Gupta +3 more
openaire +2 more sources
Cancer, Volume 132, Issue 3, 1 February 2026.Abstract Background Malignant peripheral nerve sheath tumors (MPNSTs) are aggressive soft tissue sarcomas with a 5‐year survival rate of approximately 50%, secondary to their metastatic potential and resistance to therapy. MPNSTs can arise sporadically, as a late toxicity from therapeutic radiotherapy, or in patients with neurofibromatosis type 1 (NF1).
Rachel E. Aubrey +7 more
wiley +1 more source
Neurilemoma of the small intestine (Clinical case presentation)
Российский журнал гастроэнтерологии, гепатологии, колопроктологии, 2012 The aim of clinical case presentation. To draw attention of specialists to rare neoplastic bowel diseases.Original points. Article presents the case of small intestinal neurilemoma in 69 years-old woman with incidental abdominal pain.
I. D. Kalganov +3 more
doaj
Ancient schwannoma of the orbit
Oman Journal of Ophthalmology, 2014 The ancient schwannoma is a rare variant of a neurilemoma with a course typical of a slow-growing benign neoplasm. Histologically, it can be confused with a malignant mesenchymal tumor because of increased cellularity, nuclear pleomorphism, and ...
Anjali S Kulkarni +4 more
doaj +1 more source
Retroperitoneal schwannoma: A common tumour in an uncommon site [PDF]
, 2010 We describe a female adult patient who presented with acute retention of urine and vague abdominal discomfort. A provisional diagnosis of ovarian tumour was made after crosssectional imaging.
Chu, TYC, Tam, KF, Wong, CS
core
Clinicopathologic analysis of 7 cases of oral schwannoma and review of the literature? [PDF]
, 2010 Schwannomas, also known as neurilemmomas, are uncommon neoplasms apparently derived from Schwann cells. The growth of these tumors causes displacement and compression of the nerve of origin.
Freitas, Roseana de Almeida +4 more
core +1 more source