Case Report
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Year 2022, Volume: 6 Issue: 4, 537 - 539, 01.04.2022
https://doi.org/10.28982/josam.947348

Abstract

Supporting Institution

YOK

Project Number

YOK

References

  • 1. Ferry JA, Dickersin GR. Pseudoglandular schwannoma. Am J Clin Pathol. 1988;89(4):546–52.
  • 2. Chan JKC, Fok KO. Pseudoglandular schwannoma. Histopathology 1996;29:481–3.
  • 3. Robinson CA, Curry B, Rewcastle NB. Pseudoglandular elements in schwannoma. Arch Pathol Lab Med. 2005;129:1106–12.
  • 4. Ud Din N, Ahmad Z, Ahmed, A. Schwannomas with pseudoglandular elements: clinicopathologic study of 61 cases. Ann Diagn Pathol. 2016;20:24–28.
  • 5. Ruggeri F, De Cerchio L, Bakacs A, Orlandi A, Lunardi P. Pseudoglandular schwannoma of the cauda equina. J Neurosurg Spine. 2006;5:543–45.
  • 6. Brooks JJ, Draffen RM. Benign glandular schwannoma. Arch Pathol Lab Med. 1992; 116:192–5.
  • 7. Fletcher CDM, Madziwa D, Heydermm E, McKee PH. Benign dermal schwannoma with glandular elements—true heterology or a local “organizer” effect? Clin Exp Dermatol. 1986;11:475–85.
  • 8. Deng A, Petrali J, Jaffe D, Sina B, Gaspari A. Benign cutaneous pseudoglandular schwannoma. A case report. Am J Dermatopathol. 2005;27:432–5.
  • 9. Rishi K, Coffey D, Javed R, Powell S, Takei H. Immunohistochemical comparison of spindle cell lesions: Schwannoma versus fibroblastic meningioma. FASEB J. 2007;21:389.
  • 10. Park JY, Park H, Park NJ, Park JS, Sung HJ, Lee SS. Use of calretinin, CD56, and CD34 for differential diagnosis of schwannoma and neurofibroma. Korean J Pathol 2011; 45:30–5.
  • 11. Sundarkrishnan L, Bradish JR, Oliai BR, Hosler GA. Cutaneous Cellular Pseudoglandular Schwannoma: An Unusual Histopathologic Variant. Am J Dermatopathol.2016;38(4):315–8.
  • 12. Aksoy A, Sır E. Results of surgical treatment of ulnar nerve schwannomas arising from upper extremity: Presentation of 15 cases with review of literature. J Surg Med. 2019;3(2):159-62.

A rare case of pseudoglandular schwannoma

Year 2022, Volume: 6 Issue: 4, 537 - 539, 01.04.2022
https://doi.org/10.28982/josam.947348

Abstract

A pseudoglandular schwannoma is a rare benign tumor. Controversy in the literature regarding the histogenesis of pseudoglandular schwannoma exists. Histological features of pseudoglandular schwannomas are different than those found in classical schwannomas. A patient with pseudoglandular schwannomas has a good prognosis, and no cases of recurrence have been reported in the literature.

Project Number

YOK

References

  • 1. Ferry JA, Dickersin GR. Pseudoglandular schwannoma. Am J Clin Pathol. 1988;89(4):546–52.
  • 2. Chan JKC, Fok KO. Pseudoglandular schwannoma. Histopathology 1996;29:481–3.
  • 3. Robinson CA, Curry B, Rewcastle NB. Pseudoglandular elements in schwannoma. Arch Pathol Lab Med. 2005;129:1106–12.
  • 4. Ud Din N, Ahmad Z, Ahmed, A. Schwannomas with pseudoglandular elements: clinicopathologic study of 61 cases. Ann Diagn Pathol. 2016;20:24–28.
  • 5. Ruggeri F, De Cerchio L, Bakacs A, Orlandi A, Lunardi P. Pseudoglandular schwannoma of the cauda equina. J Neurosurg Spine. 2006;5:543–45.
  • 6. Brooks JJ, Draffen RM. Benign glandular schwannoma. Arch Pathol Lab Med. 1992; 116:192–5.
  • 7. Fletcher CDM, Madziwa D, Heydermm E, McKee PH. Benign dermal schwannoma with glandular elements—true heterology or a local “organizer” effect? Clin Exp Dermatol. 1986;11:475–85.
  • 8. Deng A, Petrali J, Jaffe D, Sina B, Gaspari A. Benign cutaneous pseudoglandular schwannoma. A case report. Am J Dermatopathol. 2005;27:432–5.
  • 9. Rishi K, Coffey D, Javed R, Powell S, Takei H. Immunohistochemical comparison of spindle cell lesions: Schwannoma versus fibroblastic meningioma. FASEB J. 2007;21:389.
  • 10. Park JY, Park H, Park NJ, Park JS, Sung HJ, Lee SS. Use of calretinin, CD56, and CD34 for differential diagnosis of schwannoma and neurofibroma. Korean J Pathol 2011; 45:30–5.
  • 11. Sundarkrishnan L, Bradish JR, Oliai BR, Hosler GA. Cutaneous Cellular Pseudoglandular Schwannoma: An Unusual Histopathologic Variant. Am J Dermatopathol.2016;38(4):315–8.
  • 12. Aksoy A, Sır E. Results of surgical treatment of ulnar nerve schwannomas arising from upper extremity: Presentation of 15 cases with review of literature. J Surg Med. 2019;3(2):159-62.
There are 12 citations in total.

Details

Primary Language English
Subjects Pathology
Journal Section Case report
Authors

Fadime Eda Gökalp Satıcı 0000-0002-3103-7856

Hamide Sayar 0000-0002-8273-2605

Project Number YOK
Publication Date April 1, 2022
Published in Issue Year 2022 Volume: 6 Issue: 4

Cite

APA Gökalp Satıcı, F. E., & Sayar, H. (2022). A rare case of pseudoglandular schwannoma. Journal of Surgery and Medicine, 6(4), 537-539. https://doi.org/10.28982/josam.947348
AMA Gökalp Satıcı FE, Sayar H. A rare case of pseudoglandular schwannoma. J Surg Med. April 2022;6(4):537-539. doi:10.28982/josam.947348
Chicago Gökalp Satıcı, Fadime Eda, and Hamide Sayar. “A Rare Case of Pseudoglandular Schwannoma”. Journal of Surgery and Medicine 6, no. 4 (April 2022): 537-39. https://doi.org/10.28982/josam.947348.
EndNote Gökalp Satıcı FE, Sayar H (April 1, 2022) A rare case of pseudoglandular schwannoma. Journal of Surgery and Medicine 6 4 537–539.
IEEE F. E. Gökalp Satıcı and H. Sayar, “A rare case of pseudoglandular schwannoma”, J Surg Med, vol. 6, no. 4, pp. 537–539, 2022, doi: 10.28982/josam.947348.
ISNAD Gökalp Satıcı, Fadime Eda - Sayar, Hamide. “A Rare Case of Pseudoglandular Schwannoma”. Journal of Surgery and Medicine 6/4 (April 2022), 537-539. https://doi.org/10.28982/josam.947348.
JAMA Gökalp Satıcı FE, Sayar H. A rare case of pseudoglandular schwannoma. J Surg Med. 2022;6:537–539.
MLA Gökalp Satıcı, Fadime Eda and Hamide Sayar. “A Rare Case of Pseudoglandular Schwannoma”. Journal of Surgery and Medicine, vol. 6, no. 4, 2022, pp. 537-9, doi:10.28982/josam.947348.
Vancouver Gökalp Satıcı FE, Sayar H. A rare case of pseudoglandular schwannoma. J Surg Med. 2022;6(4):537-9.