1999
DOI: 10.1007/s005950050651
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Pancreatic schwannoma: Report of a case

Abstract: We present herein a case of solitary schwannoma of the pancreas and also review 26 previously reported cases from the English and Japanese literature. Primary schwannoma of the pancreas is a rare tumor. A 50-year-old female was discovered to have a large mass in the upper abdomen on ultrasonography. An examination by computed tomography (CT) scan, magnetic resonance imaging (MRI), and ultrasonography revealed a solid and cystic tumor in the left upper quadrant of the abdomen. A distal pancreatectomy with a spl… Show more

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Cited by 40 publications
(22 citation statements)
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“…[1][2][3]11,12 The pancreas, however, is an extremely unusual site of origin for these tumors. [2][3][4][5] To our knowledge, only 32 cases of pancreatic schwannoma have been reported in the English language literature, which are summarized in Table 1.…”
Section: Discussionmentioning
confidence: 98%
“…[1][2][3]11,12 The pancreas, however, is an extremely unusual site of origin for these tumors. [2][3][4][5] To our knowledge, only 32 cases of pancreatic schwannoma have been reported in the English language literature, which are summarized in Table 1.…”
Section: Discussionmentioning
confidence: 98%
“…In the literature, only 29 cases of intrapancreatic schwannoma have been previously reported [1,4,6]. These 29 cases demonstrated that schwannoma of the pancreas is a tumor generally found in older adults, in a nearly equal ratio of men to women.…”
Section: Sirmentioning
confidence: 88%
“…Schwannoma of the pancreas is an extremely rare lesion; only 29 cases have been reported in the present era [1,4,6]. In the literature, pancreatic schwannomas are reported as often showing cystic features, clinically mimicking pseudocysts or cystic tumors.…”
Section: Sirmentioning
confidence: 97%
“…Recurrently reported tumors include, among few other entities, malignant peripheral nerve sheath tumors (MPNST) [7,8,9,10,14,19]. In general, MPNST may arise either sporadically or in association with hereditary neurofibromatosis (types 1 and 2).…”
Section: Introductionmentioning
confidence: 99%