This study presents a case of a 45-year-old male with a laryngeal granular cell tumor (diagnosed via histology and staining), who was treated with plasma ablation without recurrence.
Case Report
This study presents a case of a 45-year-old male with a laryngeal granular cell tumor (diagnosed via histology and staining), who was treated with plasma ablation without recurrence.
Granular cell tumor (GCT) is a rare benign neoplasm that most commonly arises in the head and neck region. Laryngeal involvement is exceptional. A 45-year-old man presented with a 3-year history of progressive hoarseness without apparent precipitating factors. Occasional cough produced white, viscous sputum; neither dyspnea nor dysphagia was reported. Laryngoscopy revealed a smooth-surfaced, broad-based elevation involving the anterior two-thirds of the right true vocal fold. Histology revealed polygonal cells with abundant granular cytoplasm and a low nuclear-to-cytoplasmic ratio, set within a delicate fibrovascular stroma. Periodic acid-Schiff staining highlighted cytoplasmic granules. Immunohistochemistry demonstrated diffuse positivity for S-100, CD68, and neuron-specific enolase (NSE), confirming the diagnosis of GCT. The lesion was completely excised in two stages using low-temperature plasma radiofrequency ablation (LTP-RFA). At 24 months of follow-up, no evidence of recurrence was observed. GCT may be mistaken histologically for squamous cell carcinoma (SCC). Recognition of this differential diagnosis is essential for otolaryngologists.
Granular cell tumor (GCT, Abrikossoff tumor) was first described in 1926 and popularized by Abrikossoff in 19621. The cytoplasm exhibits a granular appearance resulting from lysosomal aggregation, leading to the designation "granular cell tumor". Current evidence suggests a neurogenic origin, with immunohistochemical and ultrastructural findings supporting derivation from Schwann cells or their precursors2. GCT can occur at any age and at any site3. Peak incidence occurs in adults aged 40-60 years4. The incidence of multifocal GCT in adults is 5%-16%5. Around 30%-50% occur in the head and neck, with 3%-10% in the larynx2, and involvement of the vocal cords is extremely rare. In adults, lesions predominate in the posterior one-third of the vocal cords, whereas pediatric cases more frequently affect the anterior vocal cords and subglottis. Additional reported sites include the anterior commissure, cricoid cartilage, false vocal cords, subglottic region, and posterior cricoid area6.
GCT produces varied clinical manifestations and histological overlap with laryngeal carcinoma7, which frequently results in misdiagnosis or unnecessary extensive surgery. The present case report delineates clinical presentation, diagnostic work-up, treatment, and prognosis of vocal cord granular cell tumor, supplying clinicians with a reference to minimize misdiagnosis and overtreatment while enhancing disease recognition and management.
CASE PRESENTATION:
A 45-year-old male presented with persistent hoarseness for more than 3 years without apparent precipitating factors. Occasional cough produced white, viscous sputum; neither dyspnea nor dysphagia was reported. Past medical history included laryngopharyngeal reflux and a 20-year smoking habit of approximately twenty cigarettes per day; alcohol was consumed sporadically. No long-term medication use or family history of head and neck cancer was documented.
Evaluation at a local community hospital included two laryngoscopic examinations that revealed a right vocal cord mass requiring further assessment (Figure 1). Differential diagnoses of vocal cord cyst and vocal cord leukoplakia were proposed.
Diagnosis, Assessment, and Plan:
Rigid laryngoscopy revealed extensive thickening and protrusion of the anterior-to-mid right vocal cord; both cords remained mobile. Contrast-enhanced neck MRI (1.5 T) demonstrated mild right vocal cord thickening, normal contralateral cord, absence of surrounding-tissue invasion or bone destruction, and no cervical lymph-node enlargement (Figure 2). Chest CT excluded pulmonary metastases. Under general anesthesia, microlaryngoscopy with a suspension laryngoscope was performed. Cold-instrument palpation indicated a firm, rubbery consistency (Figure 3). Surface tissue was peeled away; deeper tissue was sampled and submitted for histology. To preserve the vocal ligament, conservative debulking with plasma-field ablation was carried out. Post-operative course remained uneventful; voice rest and inhaled corticosteroid nebulization were instituted.
Histology revealed focal mucosal hyperplasia with erosion; stromal cells displayed an elevated nuclear-to-cytoplasmic ratio and abundant granular cytoplasm (Figure 4). Immunohistochemistry demonstrated negative cytokeratin (CK) and vimentin, whereas S-100 protein (Figure 5) and neuron-specific enolase (NSE) were positive, consistent with neurogenic differentiation.CD68 positivity suggested either phagocytic capacity or a reparative phenotype. Scattered Ki-67-positive nuclei indicated low proliferative activity. Special stains showed positive Periodic Acid-Schiff (PAS) and negative Congo red. Collectively, these findings support a diagnosis of granular cell tumor.
Laryngoscopy revealed residual right vocal cord thickening 30 days postoperatively; hoarseness persisted. Microlaryngoscopy with suspension laryngoscopy was repeated 5 months later, again employing plasma ablation. Subsequent examination revealed well-healed vocal cords with complete epithelial regeneration, satisfactory glottic closure, no evidence of tumor recurrence, and marked voice improvement. Follow-up laryngoscopy at 8 months confirmed the absence of recurrence (Figure 6).
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The research protocol adheres to the guidelines of the Ethics Committee for Human Research at Hangzhou First People's Hospital. Written informed consent for participation was obtained from the patient.
1. Preoperative preparation
2. Surgical procedure
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In this case report, two microlaryngoscopic surgeries under suspension laryngoscopy were performed on the patient. For the first surgery, to ensure the integrity of the patient's vocal ligament, a conservative tumor resection was performed. Five months later, the second surgery was performed, during which the tumor tissue was completely removed. Pathological examination revealed the following findings: for the 'vocal cord (frozen section + routine specimen submission)', the mucosal tissue...
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GCT is characterized by slow growth and insidious symptoms8. The most common symptoms of laryngeal granular cell tumor are dysphonia and hoarseness, but cough, dysphagia, and odynophagia may also occur9. Under laryngoscopy, GCT can have various morphologies, and it is difficult to distinguish it from polyps, cysts, and malignant tumors with the naked eye. It must be confirmed by pathological examination. Differential diagnoses that should be considered include laryngeal cys...
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The authors have nothing to disclose
This work was supported by the National Key Research and Development Program of China (Grant No. 2022YFC2504100), the Zhejiang Provincial Traditional Chinese Medicine Science and Technology Project (Grant No. 2023ZL569), and the Hangzhou Municipal Health Commission’s Special Program (Grant No. 2021WJCY044).
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| Name | Company | Catalog Number | Comments |
|---|---|---|---|
| Disposable RF plasma scalpel head | Shenzhen Viewwall Medical Technology Co., Ltd. | VAM-Q-3830230 | Sterile, ethylene oxide sterilized, disposable |
| Laryngeal endoscope | KARLSTORZ Germany | 8714AA | Sterile,dry heat sterilized, reusable |
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