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Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location

Patient: Male, 21-year-old Final Diagnosis: Ancient schwannoma Symptoms: Facial swelling Medication: — Clinical Procedure: — Specialty: Dentistry • Pathology OBJECTIVE: Rare disease BACKGROUND: Schwannoma is an uncommon benign tumor that develops from Schwann cells in the peripheral nervous system;...

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Autor principal: Alotaiby, Faraj
Formato: Online Artículo Texto
Lenguaje:English
Publicado: International Scientific Literature, Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793338/
https://www.ncbi.nlm.nih.gov/pubmed/36560857
http://dx.doi.org/10.12659/AJCR.938335
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author Alotaiby, Faraj
author_facet Alotaiby, Faraj
author_sort Alotaiby, Faraj
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description Patient: Male, 21-year-old Final Diagnosis: Ancient schwannoma Symptoms: Facial swelling Medication: — Clinical Procedure: — Specialty: Dentistry • Pathology OBJECTIVE: Rare disease BACKGROUND: Schwannoma is an uncommon benign tumor that develops from Schwann cells in the peripheral nervous system; 25–50% of such tumors occur in the head and neck. A rare variety of schwannoma, known as an ancient schwannoma, exhibits calcification, cystic degeneration, hemorrhage, myxoid stroma, pleomorphism, and nuclear hyperchromatism. Such characteristics may contribute to this tumor being incorrectly diagnosed as malignant. Almost all reported intra-oral ancient schwannomas behave innocuously. CASE REPORT: A 20-year-old man presented to the oral surgery clinic with a right facial swelling that began a few months before. CT and MRI were performed and showed a well-defined cystic lesion anterior to the right masseter muscle, located in the subcutaneous area and measuring 28×24×20 mm. No extension to the surrounding tissues nor any other similar lesions were seen. Microscopic examination revealed an encapsulated nodular mass with cystic cavities, hemorrhage, and variably distributed myxoid and hyalinized stroma. The tumor demonstrated 2 distinct cell distributions: hypercellular areas (Antoni A) and myxoid hypocellular areas (Antoni B). Focal areas in high-power magnification showed atypical cells with hyperchromatic and pleomorphic nuclei. The tumor cells showed diffuse positivity for S-100 in IHC. The diagnosis of ancient schwannoma was made. At 1-year follow-up, there was no evidence of nerve injury or recurrence. CONCLUSIONS: One more case of oral ancient schwannoma is added to the literature. This is the first reported in Saudi Arabia. It is prudent to be familiar with the degenerative and cytologic alterations of ancient schwannoma, as this may limit the likelihood of misdiagnosis and unnecessary treatment of this benign tumor, with an excellent prognosis.
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spelling pubmed-97933382023-01-04 Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location Alotaiby, Faraj Am J Case Rep Articles Patient: Male, 21-year-old Final Diagnosis: Ancient schwannoma Symptoms: Facial swelling Medication: — Clinical Procedure: — Specialty: Dentistry • Pathology OBJECTIVE: Rare disease BACKGROUND: Schwannoma is an uncommon benign tumor that develops from Schwann cells in the peripheral nervous system; 25–50% of such tumors occur in the head and neck. A rare variety of schwannoma, known as an ancient schwannoma, exhibits calcification, cystic degeneration, hemorrhage, myxoid stroma, pleomorphism, and nuclear hyperchromatism. Such characteristics may contribute to this tumor being incorrectly diagnosed as malignant. Almost all reported intra-oral ancient schwannomas behave innocuously. CASE REPORT: A 20-year-old man presented to the oral surgery clinic with a right facial swelling that began a few months before. CT and MRI were performed and showed a well-defined cystic lesion anterior to the right masseter muscle, located in the subcutaneous area and measuring 28×24×20 mm. No extension to the surrounding tissues nor any other similar lesions were seen. Microscopic examination revealed an encapsulated nodular mass with cystic cavities, hemorrhage, and variably distributed myxoid and hyalinized stroma. The tumor demonstrated 2 distinct cell distributions: hypercellular areas (Antoni A) and myxoid hypocellular areas (Antoni B). Focal areas in high-power magnification showed atypical cells with hyperchromatic and pleomorphic nuclei. The tumor cells showed diffuse positivity for S-100 in IHC. The diagnosis of ancient schwannoma was made. At 1-year follow-up, there was no evidence of nerve injury or recurrence. CONCLUSIONS: One more case of oral ancient schwannoma is added to the literature. This is the first reported in Saudi Arabia. It is prudent to be familiar with the degenerative and cytologic alterations of ancient schwannoma, as this may limit the likelihood of misdiagnosis and unnecessary treatment of this benign tumor, with an excellent prognosis. International Scientific Literature, Inc. 2022-12-23 /pmc/articles/PMC9793338/ /pubmed/36560857 http://dx.doi.org/10.12659/AJCR.938335 Text en © Am J Case Rep, 2022 https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under Creative Common Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0 (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Articles
Alotaiby, Faraj
Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title_full Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title_fullStr Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title_full_unstemmed Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title_short Ancient Schwannoma: Case Report of an Unusual Entity in an Unusual Oral Location
title_sort ancient schwannoma: case report of an unusual entity in an unusual oral location
topic Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9793338/
https://www.ncbi.nlm.nih.gov/pubmed/36560857
http://dx.doi.org/10.12659/AJCR.938335
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