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Journals / Journal of Surgery and Medicine / 2026 / Cilt: 6 Sayı: 4

A rare case of pseudoglandular schwannoma

Fadime Eda Gökalp Satıcı(MERSIN UNIVERSITY, SCHOOL OF MEDICINE)0000-0002-3103-7856
Hamide Sayar(MERSİN ÜNİVERSİTESİ, TIP FAKÜLTESİ, CERRAHİ TIP BİLİMLERİ BÖLÜMÜ, TIBBİ PATOLOJİ ANABİLİM DALI)0000-0002-8273-2605
Pages
537–539
Publication Date
2022-04-01
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AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

A patient with pseudoglandular schwannomas has a good prognosis, and no cases of recurrence have been reported in the literature.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:A pseudoglandular schwannoma is a rare benign tumor.
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Key Findings & Data:Controversy in the literature regarding the histogenesis of pseudoglandular schwannoma exists.
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Conclusion & Impact:A patient with pseudoglandular schwannomas has a good prognosis, and no cases of recurrence have been reported in the literature.
🔬Design:Olgu Sunumu
📍Scope:Comprehensive Sample
⚙️Variables:Pseudoglandular schwannoma · Pseudocyst · Schwannoma

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.

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Cite This Article

Satıcı, F. E. G., Sayar, H. (2022). A rare case of pseudoglandular schwannoma. Journal of Surgery and Medicine, Cilt: 6 Sayı: 4, 537–539. https://doi.org/10.28982/josam.947348

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References (12)

  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.