Publish in this journal
Journal Information
Vol. 84. Num. 4.July - August 2018Pages 401-528
Share
Share
Download PDF
More article options
Visits
1918
Vol. 84. Num. 4.July - August 2018Pages 401-528
Case report
DOI: 10.1016/j.bjorl.2015.12.007
A rare laryngeal tumor in a patient with thyroid papillary cancer: granular cell tumor
Um raro tumor de laringe em paciente com carcinoma papilífero da tireoide: tumor de células granulares
Visits
1918
Sheng-Yao Chenga, Li-Hsiang Chenga,
Corresponding author
m1041000@mail.ndmctsgh.edu.tw

Corresponding author.
, Yi-Shu Liaob, Wen-Sen Laic
a National Defense Medical Center, Tri-Service General Hospital, Department of Otolaryngology–Head and Neck Surgery, Taipei, Taiwan
b National Defense Medical Center, Tri-Service General Hospital, Department of Pathology, Taipei, Taiwan
c Taichung Armed Forces General Hospital, Department of Otolaryngology-Head and Neck Surgery, Taichung, Taiwan
This item has received
1918
Visits
Article information
Full Text
Bibliography
Download PDF
Statistics
Figures (3)
Show moreShow less
Tables (1)
Table 1. Vocal fold lesions.
Full Text
Introduction

Granular cell tumor (GCT), Abrikossoff's tumor, is a rare tumor, especially that occurring in the larynx. It may share similar appearance and symptoms with laryngeal granuloma, polyp, or nodule although they have different etiology and features (Table 1). The diagnosis must be made by histological examination. In the past decades, the origin of GCT remained controversial but current mainstream opinion regarded it as of neuroectodermal origin according to immunohistochemical staining.1 Here we presented a patient with a history of papillary thyroid carcinoma under regular follow-up who was diagnosed recently with a GCT of the larynx. The related literatures were also reviewed.

Table 1.

Vocal fold lesions.

Vocal fold lesions  Features  Common causes  Treatment 
NoduleUsually bilateral  Chronic voice abuse  Speech therapy 
Smaller    Excision 
PolypOften unilateral  Acute voice abuse  Behavior modification (quit smoking, speech therapy)
Obvious surface  Chronic irrigation (For example, smoking, gastroesophageal reflux)
Blood vessel  Excision 
GranulomaOften bilateral  Repeated trauma (For example, intratracheal intubation)Excision 
Larger   
Granular cell tumorSingle  UnknownExcision
Unilateral 
Most common at posterior glottis 
Case report

A 35-year-old female presented with a 10 month history of progressive painless hoarseness and easy voice fatigue. Three years ago, she was diagnosed with papillary thyroid cancer and received total thyroidectomy and Iodine-131 therapy. Since then, she has been under daily levothyroxine supplement (0.1mg per day) and regular follow-up. She has been smoking 20 cigarettes per day over 10 years but without voice abuse history. There was no palpable neck mass on physical examination. Due to the persistent symptom, she came to our clinic where indirect laryngoscope showed a white tumor lesion at right posterior third vocal fold with mucosal cover and unclear border which led to failure of glottis closure during phonation (Fig. 1). Because of her history and the appearance of tumor, primary laryngeal malignancy or recurrent papillary thyroid carcinoma metastasis was suspected. The tumor was completely excised through microlaryngeal surgery with cold knife under general anesthesia. The lesion measured about 0.5cm×0.2cm in size and was totally embedded for sections. Histopathologic examination revealed one nodular lesion with pseudoepitheliomatous hyperplasia. Under hematoxylin-eosin (H&E) staining, polygonal cells with abundant eosinophilic granular cytoplasm and small uniform nuclei arranged in nests was impressed (Fig. 2). There was no evidence of malignancy due to the absence of pleomorphism with small nuclei.

Figure 1.
(0.09MB).

Preoperative indirect laryngoscope finding: a white tumor lesion was at right vocal fold with mucosal cover and unclear border which led to failure of glottis closure during phonation.

Figure 2.
(0.24MB).

The tumor comprised round or polygonal cells with abundant eosinophilic granular cytoplasm and small uniform nuclei arranged in nest and sheet patterns (H&E, 400×).

Immunohistochemical staining showed positive for S-100 protein (Fig. 3A), vimentin and neuron-specific enolase (Fig. 3B). The tumor was uniformly negative for thyroglobulin, TTF1, and HBME-1. According to the above pathologic results, the final diagnosis was laryngeal granular cell tumor. After 6 months of follow-up, she was satisfied with her voice outcome and no local tumor recurrence was noted.

Figure 3.
(0.35MB).

(A) Positive S-100 immunostain. (B) Positive neuron-specific enolase immunohistochemical staining denoted its neuroectodermal origin.

Discussion

Most cases of papillary thyroid cancer had laryngeal involvement through direct invasion and were regarded as advanced stage. Although papillary thyroid carcinoma tends to spread via the lymphatic system, manifesting as laryngeal metastatic nodules, hematogenous spread had also been reported before.2 The patient had a thyroid cancer history and was under regular follow-up after total thyroidectomy. Thus, metastatic malignancy should be considered for differential diagnosis of laryngeal tumors.

GCTs are uncommon neoplasms and can be found in any organ of the whole body. About half of the cases are found in the head and neck, with the tongue being the site most affected in this region. The larynx being affected by GCT is as rare as 3–10% of all cases.3 Different from other common laryngeal lesions such as polyp or nodule, GCT showed slight female predominance, and no causal relationship between GCT and voice abuse had been established.4 The symptoms of GCTs vary with tumor size and localization. Weakening hoarseness is the most common symptom. However, lump sensation in the throat, dry cough, hemoptysis, and odynophagia can also be present.5 Grossly, laryngeal GCTs are characterized as being firm, round, mucosa-covered masses located most frequently in the posterior two-thirds of the vocal folds although other sites such as arytenoid, posterior cricoid region, supra- or subglottic areas have also been described.6

They often resemble vocal fold granulomas, polyps, and even malignant lesions. Consequently, the definite diagnosis was made by histopathological examination which demonstrated polygonal cells with thickening of the cell membrane and abundant eosinophilic intracytoplasmic granules. The origin of GCT remained controversial. It was first described by Abrikossof, in 1926, who named it as myoblastoma that was considered from skeletal muscle cells base on their cytologic picture.7 However, recent immunochemistry studies have provided better evidences of the origin of this tumor which show positive for S-100 protein, neuron-specific enolase, and CD68 but negative for muscular markers such as myoglobin, keratin, and desmin. These staining characteristics suggested that they originate from the neuroectodermal tissue or Schwann cells rather than muscle cells.4 In recent immunohistochemical study, GCTs have a component of endomesenchymal origin suggested by Simona Gurzu et al.8

Most GCTs are benign with slow growth, only 1–2% of all cases occur as malignant tumors which showed more nuclear pleomorphism, high nuclear to cytoplasmic ratio, and increased mitotic activity on histologic examination. In addition, malignant tumors tend to exceed 4cm in size with invasion of adjacent structures or metastases.1 The coexistence of GCT and other malignant neoplasms in the same organ has been reported in multiple organ including tongue and larynx.9 Sometimes, biopsy or subtotal resection was too superficial to distinguish pseudoepitheliomatous hyperplasia (PEH) which appears on the mucosal layer in half of all cases of laryngeal GCTs from squamous cell carcinoma.10 In view of these problems, the treatment aimed at complete excision using laser or cold instruments and minimal functional damage. After complete resection, most cases can be cured, but recurrence still presents in 2–21% of all cases, usually at the primary site.5 Therefore, the patients need to be under follow-up with laryngoscopy to confirm complete recovery.

Conclusion

In conclusion, laryngeal GCT is a rare and benign tumor. However, the possibility of coexistence with malignant neoplasm and voice disturbance were of concern. Complete resection with laser or cold knife for pathologic examination should be performed. To our best knowledge, this is the first case of glottic GCT in patients receiving levothyroxine supplement after total thyroidectomy. In this patient, although we cannot provide evidence that tumor growth is mediated by levothyroxine stimulation; more cases should be collected for analysis to understand the etiology of this rare tumor.

Conflicts of interest

The authors declare no conflicts of interest.

References
[1]
J.B. White,R. Glade,C.T. Rossi,S. Bielamowicz
Granular cell tumors of the larynx: diagnosis and management
[2]
A.H. Hakeem,S.A. Pradhan,S. Bhele,J. Tubachi
Metastasis of papillary thyroid cancer to the larynx and pharynx: unusual case report
Eur Arch Otorhinolaryngol, 269 (2012), pp. 2585-2587 http://dx.doi.org/10.1007/s00405-012-2149-6
[3]
R.H. Lazar,R.T. Younis,E.A. Kluka,R.E. Joyner,S. Storgion
Granular cell tumor of the larynx: report of two pediatric cases
Ear Nose Throat J, 71 (1992), pp. 440-443
[4]
C. Arevalo,B. Maly,R. Eliashar,M. Gross
Laryngeal granular cell tumor
[5]
J.H. Park,N.Y. Do,S.I. Cho,J.Y. Choi
Granular cell tumor on larynx
Clin Exp Otorhinolaryngol, 3 (2010), pp. 52-55 http://dx.doi.org/10.3342/ceo.2010.3.1.52
[6]
S. Aydin,A. Sanh,O. Celebi,E. Ayduran,G. Melin
Laryngeal granular cell tumor; rare location
Acta Med, 54 (2011), pp. 41-43
[7]
A.J. Abrikossoff
Uber myome
Virchow Arch A, 260 (1926), pp. 215-233
[8]
S. Gurzu,D. Ciortea,A. Tamasi,M. Golea,A. Bodi,D.I. Sahlean
The immunohistochemical profile of granular cell (Abrikossoff) tumor suggests an endomesenchymal origin
Arch Dermatol Res, 307 (2015), pp. 151-157 http://dx.doi.org/10.1007/s00403-014-1505-3
[9]
H.Y. Son,J.P. Kim,G.H. Ko,E.J. Lee,S.H. Woo
Lingual squamous cell carcinoma surrounded by granular cell tumor
Chonnam Med J, 48 (2012), pp. 65-68 http://dx.doi.org/10.4068/cmj.2012.48.1.65
[10]
D. Lv,S. Liu,R. Yu,Y. Zhu,H. Yang
Diagnosis and management of granular cell tumor of the larynx
J Clin Otolaryngol Head Neck Surg, 27 (2013), pp. 116-118

Please cite this article as: Cheng S-Y, Cheng L-H, Liao Y-S, Lai W-S. A rare laryngeal tumor in a patient with thyroid papillary cancer: granular cell tumor. Braz J Otorhinolaryngol. 2018;84:519–22.

Peer Review under the responsibility of Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial.

Copyright © 2016. Associação Brasileira de Otorrinolaringologia e Cirurgia Cérvico-Facial
Idiomas
Brazilian Journal of Otorhinolaryngology (English Edition)

Subscribe to our Newsletter

Article options
Tools
Cookies policy
To improve our services and products, we use cookies (own or third parties authorized) to show advertising related to client preferences through the analyses of navigation customer behavior. Continuing navigation will be considered as acceptance of this use. You can change the settings or obtain more information by clicking here.