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Published in: Diagnostic Pathology 1/2019

Open Access 01-12-2019 | Gastrointestinal Stromal Tumor | Case Report

A rare simultaneous coexistence of epithelioid gastrointestinal stromal tumors and schwannoma in the stomach: a case report

Authors: Yuxin Li, Yongliang Teng, Xiaofei Wei, Zhuang Tian, Yuqing Cao, Xiaona Liu, Xiumei Duan

Published in: Diagnostic Pathology | Issue 1/2019

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Abstract

Background

Gastrointestinal stromal tumors (GISTs), a type of mesenchymal tumor in the gastrointestinal tract, are believed to be closely associated with PDGFRA and C-KIT mutations. Schwannoma in the stomach, which is an unusual location, is a rare disorder. The simultaneous occurrence of the two diseases is rarer than metachronous occurrences, and its pathological characteristics have not been reported to date. We present a case report on a patient with simultaneous coexistence of gastric schwannoma and GISTs.

Case presentation

A 39-year-old female visited our hospital complaining of intermittent abdominal pain for the previous 3 months. CT revealed a 3.4 cm slight homogeneous enhancement in the lesser curvature of the stomach; the mass was nodular soft tissue, which was removed by radical surgery. Two solid tumors with different volumes were located in the stomach. Histologically and immunohistochemically different, the larger tumor consisted of spindle cells surrounded by a peripheral lymphoid cuff, and was positive for S-100. The larger tumor was therefore classified as a gastric schwannoma. The smaller tumor was composed of medium-sized round, oval cells with amphiphilic granular cytoplasm; vacuolization was also observed. The tumor cells were positive for DOG1 and sporadically positive for CD34 and CD117. Hence, the smaller tumor was diagnosed as epithelioid GISTs. Sanger sequencing revealed that the GIST tumor cells contained a deletion mutation (c.2527_2538 del12,843–846del4), which was located in exon 18 of PDGFRA.

Conclusion

GISTs combined with gastric schwannoma are a considerably rare subgroup of gastric tumors. Related clinical research is comparatively weak, and the mechanism remains unknown. We reviewed related articles to provide knowledge to improve the correct identification, diagnosis and management of patients with gastric cancer. All pathologists involved in the diagnosis and clinicians involved in the treatment should be aware of this new kind of disease pattern to improve their understanding of the disease.
Literature
1.
go back to reference Søreide K, Sandvik OM, Søreide JA, Giljaca V, Jureckova A, et al. Global epidemiology of gastrointestinal stromal tumours (GIST): a systematic review of population-based cohort studies. Cancer Epidemiol. 2016;40:39–46.CrossRef Søreide K, Sandvik OM, Søreide JA, Giljaca V, Jureckova A, et al. Global epidemiology of gastrointestinal stromal tumours (GIST): a systematic review of population-based cohort studies. Cancer Epidemiol. 2016;40:39–46.CrossRef
2.
go back to reference Tao K, Chang W, Zhao E, Deng R, Gao J, et al. Clinicopathologic features of gastric Schwannoma. Medicine (Baltimore). 2015;94(45):e1970.CrossRef Tao K, Chang W, Zhao E, Deng R, Gao J, et al. Clinicopathologic features of gastric Schwannoma. Medicine (Baltimore). 2015;94(45):e1970.CrossRef
3.
go back to reference Gopie P, Mei L, Faber AC, Grossman SR, Smith SC, et al. Classification of gastrointestinal stromal tumor syndromes. Endocr Relat Cancer. 2018;25(2):R49–58.CrossRef Gopie P, Mei L, Faber AC, Grossman SR, Smith SC, et al. Classification of gastrointestinal stromal tumor syndromes. Endocr Relat Cancer. 2018;25(2):R49–58.CrossRef
4.
go back to reference Markku M, Jerzy L. Gastrointestinal stromal tumors. Gastroenterol Clin N Am. 2013;42(2):399–415.CrossRef Markku M, Jerzy L. Gastrointestinal stromal tumors. Gastroenterol Clin N Am. 2013;42(2):399–415.CrossRef
5.
go back to reference Liang J, Wu YL, Chen BJ, Zhang W, Tanaka Y, et al. The C-KIT receptor-mediated signal transduction and tumor-related diseases. Int J Biol Sci. 2013;9(5):413–43.CrossRef Liang J, Wu YL, Chen BJ, Zhang W, Tanaka Y, et al. The C-KIT receptor-mediated signal transduction and tumor-related diseases. Int J Biol Sci. 2013;9(5):413–43.CrossRef
6.
go back to reference Li Y, Gao J, Tian Y, Li J, Shen L. Interpretation of 827 cases of gastrointestinal stromal tumor C-KIT or PDGFRA gene mutation spectrum and its relationship with clinicopathological features. Chin J Gastrointest Surg. 2015;18(4):332–7. Li Y, Gao J, Tian Y, Li J, Shen L. Interpretation of 827 cases of gastrointestinal stromal tumor C-KIT or PDGFRA gene mutation spectrum and its relationship with clinicopathological features. Chin J Gastrointest Surg. 2015;18(4):332–7.
7.
go back to reference Michael S, Emmanouel D, Charikleia S, Panagiotis S, Electra P, et al. Gastrointestinal stromal tumor. World J Surg Oncol. 2009;7:61.CrossRef Michael S, Emmanouel D, Charikleia S, Panagiotis S, Electra P, et al. Gastrointestinal stromal tumor. World J Surg Oncol. 2009;7:61.CrossRef
8.
go back to reference Vassos N, Agaimy A, Hohenberger W, Croner RS. Coexistence of gastrointestinal stromal tumours (GIST) and malignant neoplasms of different origin: prognostic implications. Int J Surg. 2014;12(5):371–7.CrossRef Vassos N, Agaimy A, Hohenberger W, Croner RS. Coexistence of gastrointestinal stromal tumours (GIST) and malignant neoplasms of different origin: prognostic implications. Int J Surg. 2014;12(5):371–7.CrossRef
9.
go back to reference Fletcher CD, Berman JJ, Corless C, Gorstein F, Lasota J, et al. Diagnosis of gastrointestinal stromal tumors: a consensus approach. Hum Pathol. 2002;33(5):459–65.CrossRef Fletcher CD, Berman JJ, Corless C, Gorstein F, Lasota J, et al. Diagnosis of gastrointestinal stromal tumors: a consensus approach. Hum Pathol. 2002;33(5):459–65.CrossRef
10.
go back to reference Yang Y, Yang J, Tang L, Shi X, Wu S, et al. Missed diagnosis of gastrointestinal stromal tumor with gastric schwannomas: a case report. Clinical Misdiagnosis Mistherapy. 2017;30(28):20–1. Yang Y, Yang J, Tang L, Shi X, Wu S, et al. Missed diagnosis of gastrointestinal stromal tumor with gastric schwannomas: a case report. Clinical Misdiagnosis Mistherapy. 2017;30(28):20–1.
11.
go back to reference Lasota J, Miettinen M. Clinical significance of oncogenic KIT and PDGFRA mutations in gastrointestinal stromal tumours. Histopathol. 2008;53(3):245–66.CrossRef Lasota J, Miettinen M. Clinical significance of oncogenic KIT and PDGFRA mutations in gastrointestinal stromal tumours. Histopathol. 2008;53(3):245–66.CrossRef
12.
go back to reference Miettinen M, Lasota J. Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis. Arch Pathol Lab Med. 2006;130(10):1466–78. Miettinen M, Lasota J. Gastrointestinal stromal tumors: review on morphology, molecular pathology, prognosis, and differential diagnosis. Arch Pathol Lab Med. 2006;130(10):1466–78.
13.
go back to reference Li J, Cai H, Wang W. Relationship between c-KIT and PDGFRA gene mutations in gastrointestinal stromal tumors and clinicopathological features, immunophenotype and prognosis. J Clin Exp Pathol. 2018;34(8):834–9. Li J, Cai H, Wang W. Relationship between c-KIT and PDGFRA gene mutations in gastrointestinal stromal tumors and clinicopathological features, immunophenotype and prognosis. J Clin Exp Pathol. 2018;34(8):834–9.
14.
go back to reference Corless CL, Schroeder A, Griffith D, Diana G, Ajia T, et al. PDGFRA mutations in gastrointestinal stromal tumors: frequency, spectrum and in vitro sensitivity to imatinib. J Clin Oncol. 2005;23(23):5357–64.CrossRef Corless CL, Schroeder A, Griffith D, Diana G, Ajia T, et al. PDGFRA mutations in gastrointestinal stromal tumors: frequency, spectrum and in vitro sensitivity to imatinib. J Clin Oncol. 2005;23(23):5357–64.CrossRef
15.
go back to reference Lasota J, Dansonka-Mieszkowska A, Sobin LH, Miettinen M. A great majority of GISTs with PDGFRA mutations represent gastric tumors of low or no malignant potential. Lab Invest. 2004;84:874–83.CrossRef Lasota J, Dansonka-Mieszkowska A, Sobin LH, Miettinen M. A great majority of GISTs with PDGFRA mutations represent gastric tumors of low or no malignant potential. Lab Invest. 2004;84:874–83.CrossRef
16.
go back to reference Debiec-Rychter M, Wasag B, Stul M, De WI, Van OA, et al. Gastrointestinal stromal tumours (GISTs) negativefor KIT (CD117 antigen)immunoreactivity. J Pathol. 2004;202:430–8.CrossRef Debiec-Rychter M, Wasag B, Stul M, De WI, Van OA, et al. Gastrointestinal stromal tumours (GISTs) negativefor KIT (CD117 antigen)immunoreactivity. J Pathol. 2004;202:430–8.CrossRef
17.
go back to reference Lopes LF, West RB, Bacchi LM, Van RM, Bacchi CE. DOG1 for the diagnosis of gastrointestinal stromal tumor (GIST): comparison between 2 different antibodies. Appl Immunohistochem Mol Morphol. 2010;18(4):333–7.CrossRef Lopes LF, West RB, Bacchi LM, Van RM, Bacchi CE. DOG1 for the diagnosis of gastrointestinal stromal tumor (GIST): comparison between 2 different antibodies. Appl Immunohistochem Mol Morphol. 2010;18(4):333–7.CrossRef
Metadata
Title
A rare simultaneous coexistence of epithelioid gastrointestinal stromal tumors and schwannoma in the stomach: a case report
Authors
Yuxin Li
Yongliang Teng
Xiaofei Wei
Zhuang Tian
Yuqing Cao
Xiaona Liu
Xiumei Duan
Publication date
01-12-2019
Publisher
BioMed Central
Published in
Diagnostic Pathology / Issue 1/2019
Electronic ISSN: 1746-1596
DOI
https://doi.org/10.1186/s13000-019-0898-x

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