原文題目(出處): A Rare Report of Two Cases: Ancient Schwannoma of Infratemporal Fossa and Verocay Schwannoma of Buccal Mucosa(Annals of Maxillofacial Surgery 2017;7;140-2) 原文作者姓名: Prerna Piyush, Sujata Mohanty, Sujoy Ghosh, Sunita Gupta 通訊作者學校: Departments of Oral Medicine and Radiology and Oral and
Maxillofacial Surgery, Maulana Azad Institute of Dental Sciences, New Delhi, India
報告者姓名(組別): 陳郁芳(A) 報告日期: 106/08/08 內文:
Abstract Schwannoma
1. A benign tumor that originates from Schwann cells of the peripheral nerve.
2. Presentation
A. Head and neck region—common B. Intraoral—rare
3. Feature A. Solitary B. Slow‑growing C. Smooth‑surfaced D. Usually asymptomatic E. Encapsulated
4. Two case—an intraoral soft tissue swelling which turned out to be
schwannoma of a) buccal mucosa b) infratemporal fossa with extension into the oral cavity
5. Diagnosis—based on complete analysis of clinical, radiological, surgical, and histopathological findings.
Introduction Schwannomas
1. Etiology and pathogenesis A. Arising from Schwann cells
B. Benign, slow‑growing, epineurium‑encapsulated neoplasms C. Comprise myelin sheaths surrounding peripheral nerves 2. Site predilection
A. Head and neck region—common(25-48%)
6. Treatment—complete excision 7. Prognosis—rarely recurrent
Case Report
Case 1—A 36 y/o male patient reported with swelling in the right facial region for 1
year.1. Extraoral examination: a mild diffuse swelling was present on the right midfacial region.
Medical history was unremarkable.
2. Intraoral examination: a 2 cm × 2 cm, sessile, firm, nontender, nonulcerated mass on the right posterior buccal mucosa
Dental history: extraction of tooth 17, 18 due to cheek biting
3. Ultrasound examination: a 30 mm × 23 mm hypoechoic mass in the soft tissue of right cheek
4. Fine‑needle aspiration cytology: inconclusive
5. Contrast‑enhanced computed tomography (in axial sections): 3.05 cm × 2.62 cm round, hypodense lesion in the right retromaxillary/infratemporal region compressing the posterior wall of maxillary sinus and anteromedially bulging into the oral cavity.
6. Treatment plan: complete surgical excision
→the entire mass was excised in total and was sent for histopathological examination.
7. The tumor consisted predominantly Antoni B pattern; bundles of palisading cells were seen with buckled nuclei(H/E)→Final diagnosis: Schwannoma
8. Prognosis: no recurrence 1 year after surgery
Case 2—A 23 y/o female patient complained of swelling in the right cheek region
for 1 year.PI: It was associated with pain of mild intensity. The patient visited a local dentist and got the extraction of 18 and 38 3 months back after which some relief was obtained but the pain reoccurred for 2 months. There was no significant medical history.
3. Magnetic resonance imaging (in coronal and axial section):
A. A 6 cm × 4.5 cm well‑defined lobulated heterogeneously enhancing lesion with solid as well as necrotic component in the right infratemporal
region.
B. Right zygomatic arch was involved with focal erosion of inner table of ramus of the mandible. There was focal erosion of right maxilla inferiorly
4. Incisional biopsy:
A. Lesional tissue was composed of neural cells with spindled nuclei B. S-100 antibody: positive(all lesional cells)
5. Treatment plan: complete surgical excision
6. Histopathological section:
A. Areas of hyalinization and myxoid change with peripherally placed nuclei.
B. Thick blood vessels with hyalinization and perivascular inflammation were noted with cystic changes.→Final diagnosis: ancient schwannoma
7. Prognosis: no recurrence 1 year after surgery
Discussion
1. Schwannoma (neurilemmoma) is a rare, benign, encapsulated perineural
A. In oral cavity: tongue
5. Ancient schwannoma: usually present as submucosal swellings with a higher
female predilection. The presenting lesion can be a primary in the
infratemporal fossa with extension into the oral cavity or vice versa.
→Similar finding was present in our report, where primary site was A. buccal mucosa in the first case
B. infratemporal fossa in the second case
C. The female gender and long‑standing history were also consistent with the literature.
6. Classification (Erlandson, 1985): seven subtypes A. classical (Verocay)
B. cellular C. plexiform D. cranial E. nerve F. melanotic
G. degenerated (ancient): when there is either cystic or fatty degeneration, focal accumulations of hyaline material, thick capsule, and infiltration of histiocytes, siderophages, and hyperchromatism.
H. granular cell
7. Treatment plan: pericapsular excision
8. Prognosis: good, rarely recurrent or malignant transform
Conclusion
1. As the clinical and radiological pictures are not distinctive, final diagnosis should be made after histopathological examination and in some cases after
immunohistochemistry analysis.
Ex. H/E, S-100 antibody…
2. The treatment of choice is complete surgical excision as recurrences and malignant transformations are exceedingly rare.
題號 題目
1 Schwannoma 最常發生在口內的哪個部位
(A) Gingiva (B) Soft palate (C) Tongue
(D) Buccal mucosa
答案(C)
出處:Oral and Maxillofacial Pathology, 4ed, P.492
題號 題目
2
下列何者不會對免疫螢光染色呈現 S-100 protein(+)的反應(A) Fibroma
(B) Schwannoma (C) Neurofibroma (D) Granular cell tumor
答案(A)
出處:Oral and Maxillofacial Pathology, 4ed, P.473,492,494,503