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Year Number of Results
1971 1
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1982 3
1983 4
1984 4
1985 1
1986 8
1987 3
1988 3
1989 4
1990 7
1991 6
1992 8
1993 3
1994 10
1995 11
1996 9
1997 7
1998 12
1999 9
2000 12
2001 7
2002 12
2003 12
2004 7
2005 11
2006 15
2007 11
2008 8
2009 11
2010 15
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2012 15
2013 15
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445 results

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Quoted phrase not found in phrase index: "Adult malignant schwannoma"
Page 1
The many faces of solitary fibrous tumor; diversity of histological features, differential diagnosis and role of molecular studies and surrogate markers in avoiding misdiagnosis and predicting the behavior.
Tariq MU, Din NU, Abdul-Ghafar J, Park YK. Tariq MU, et al. Diagn Pathol. 2021 Apr 20;16(1):32. doi: 10.1186/s13000-021-01095-2. Diagn Pathol. 2021. PMID: 33879215 Free PMC article. Review.
MAIN BODY: Apart from diversity in morphological features seen even in conventional SFT, two histologic variants (fat-forming and giant cell-rich) are also recognized. In addition, a malignant form and dedifferentiation are well recognized. Owing to diverse histological fe …
MAIN BODY: Apart from diversity in morphological features seen even in conventional SFT, two histologic variants (fat-forming and giant cell …
Intravascular schwannoma.
Gaudi S, Mills O, Goyette EF, Morgan MB. Gaudi S, et al. Am J Dermatopathol. 2011 Dec;33(8):850-4. doi: 10.1097/DAD.0b013e3181f5df90. Am J Dermatopathol. 2011. PMID: 22042258
Cutaneous schwannoma typically manifests along the course of peripheral nerves as a solitary, well-defined, skin-colored nodule within the deep dermis or subcutis of the flexor aspects of the extremities. Schwannoma enlarges slowly and typically follows a ben …
Cutaneous schwannoma typically manifests along the course of peripheral nerves as a solitary, well-defined, skin-colored nodul …
Management of Central and Peripheral Nervous System Tumors in Patients with Neurofibromatosis.
Brown R. Brown R. Curr Oncol Rep. 2023 Dec;25(12):1409-1417. doi: 10.1007/s11912-023-01451-z. Epub 2023 Oct 31. Curr Oncol Rep. 2023. PMID: 37906356 Review.
Some research suggests that alternative Mek inhibitors and other mixed tyrosine kinase inhibitors may have better efficacy in adults. Vascular endothelial growth factor (VEGF) inhibitor bevacizumab can prolong hearing and delay the need for surgery in NF2 patients with bil …
Some research suggests that alternative Mek inhibitors and other mixed tyrosine kinase inhibitors may have better efficacy in adults. …
Adrenal schwannoma.
Târcoveanu E, Dimofte G, Bradea C, Moldovanu R, Vasilescu A, Anton R, Ferariu D. Târcoveanu E, et al. JSLS. 2009 Jan-Mar;13(1):116-9. JSLS. 2009. PMID: 19366556 Free PMC article.
BACKGROUND: Adrenal schwannomas are very rare tumors that are difficult to diagnose preoperatively. We report the case of a left adrenal schwannoma incidentally discovered in a 55-year-old man during a postoperative checkup for a cutaneous malignant melanoma. ...Adr …
BACKGROUND: Adrenal schwannomas are very rare tumors that are difficult to diagnose preoperatively. We report the case of a left adrenal …
Intraocular schwannoma.
You JY, Finger PT, Iacob C, McCormick SA, Milman T. You JY, et al. Surv Ophthalmol. 2013 Jan-Feb;58(1):77-85. doi: 10.1016/j.survophthal.2012.04.003. Epub 2012 Sep 14. Surv Ophthalmol. 2013. PMID: 22981398 Review.
Uveal schwannoma has been aptly called a "pseudomelanoma", reflecting the difficulty in its clinical distinction from uveal malignant melanoma. ...Three isolated reports of uveal schwannoma with extrascleral extension exist in literature, but the prognosti …
Uveal schwannoma has been aptly called a "pseudomelanoma", reflecting the difficulty in its clinical distinction from uveal malign …
Synovial sarcoma of nerve.
Scheithauer BW, Amrami KK, Folpe AL, Silva AI, Edgar MA, Woodruff JM, Levi AD, Spinner RJ. Scheithauer BW, et al. Hum Pathol. 2011 Apr;42(4):568-77. doi: 10.1016/j.humpath.2010.08.019. Epub 2011 Feb 4. Hum Pathol. 2011. PMID: 21295819 Review.
The spectrum of the latter is broad and includes lipoma, vascular neoplasms, hematopoietic tumors, and even meningioma. Of malignant peripheral nerve neoplasms, the vast majority are primary peripheral nerve sheath tumors. ...Whereas in the past, parallels were drawn betwe …
The spectrum of the latter is broad and includes lipoma, vascular neoplasms, hematopoietic tumors, and even meningioma. Of malignant …
Benign epithelioid schwannoma.
Kindblom LG, Meis-Kindblom JM, Havel G, Busch C. Kindblom LG, et al. Am J Surg Pathol. 1998 Jun;22(6):762-70. doi: 10.1097/00000478-199806000-00015. Am J Surg Pathol. 1998. PMID: 9630185
Although an epithelioid variant of malignant schwannoma simulating carcinoma and melanoma is well recognized, a benign counterpart has not yet been defined. ...The recognition of benign epithelioid schwannoma is important because it may be misinterpreted as a …
Although an epithelioid variant of malignant schwannoma simulating carcinoma and melanoma is well recognized, a benign counter …
Neurofibrosarcoma.
Storm FK, Eilber FR, Mirra J, Morton DL. Storm FK, et al. Cancer. 1980 Jan 1;45(1):126-9. doi: 10.1002/1097-0142(19800101)45:1<126::aid-cncr2820450122>3.0.co;2-u. Cancer. 1980. PMID: 6766081
Case histories of 10 patients with neurofibrosarcoma, including 14 (70%) with neurofibromatosis, evaluated over 10 years were reviewed to determine the incidence of local and systemic recurrence and the most effective means of therapy for this rare neoplasm. ...Both A.J.C. …
Case histories of 10 patients with neurofibrosarcoma, including 14 (70%) with neurofibromatosis, evaluated over 10 years were reviewe …
Abdominal Wall Schwannoma.
Ginesu GC, Puledda M, Feo CF, Cossu ML, Fancellu A, Addis F, Porcu A. Ginesu GC, et al. J Gastrointest Surg. 2016 Oct;20(10):1781-3. doi: 10.1007/s11605-016-3164-5. Epub 2016 May 16. J Gastrointest Surg. 2016. PMID: 27184673
Schwannomas have a good prognosis overall, with malignant degeneration being very rare. Local recurrence is plausible only if non-radical resection of the primitive tumour occurs. This is the second case ever reported, to our knowledge, of symptomatic schwannoma …
Schwannomas have a good prognosis overall, with malignant degeneration being very rare. Local recurrence is plausible only if …
Pediatric neurofibrosarcoma.
Neville H, Corpron C, Blakely ML, Andrassy R. Neville H, et al. J Pediatr Surg. 2003 Mar;38(3):343-6; discussion 343-6. doi: 10.1053/jpsu.2003.50105. J Pediatr Surg. 2003. PMID: 12632346 Review.
BACKGROUND/PURPOSE: Neurofibrosarcoma is rare in children, and the natural history and prognostic factors are not well described. ...Prognosis remains poor with a high incidence of relapse, particularly in the lungs, suggesting that more aggressive therapies …
BACKGROUND/PURPOSE: Neurofibrosarcoma is rare in children, and the natural history and prognostic factors are not well describ …
445 results