CASE REPORT
The small cell carcinoma neuroendocrine type of the larynx—Case report
 
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1
Departament of Radiotherapy, Memorial Leszczyński Hospital, Katowice, Poland
 
2
Department of Laryngology, Medical University of Łódź, Norbert Barlicki Teaching Hospital, Łódź, Poland
 
3
Department of Radiology, Medical University of Łódź, Norbert Barlicki Teaching Hospital, Łódź, Poland
 
4
Department of Pathomorphology, Medical University of Łódź, Norbert Barlicki Teaching Hospital, Łódź, Poland
 
5
Department of Radiotherapy, Medical University of Silesia, Clinical Center, Katowice, Poland
 
 
Submission date: 2015-12-09
 
 
Acceptance date: 2016-06-20
 
 
Online publication date: 2016-09-12
 
 
Publication date: 2019-12-15
 
 
Pol. Ann. Med. 2017;24(1):60-63
 
KEYWORDS
ABSTRACT
Introduction:
Extrapulmonary small cell carcinoma neuroendocrine type (ESCCNET) is a rare tumor (2.5%-4.0% of all small cell carcinomas), and during the past 30 years, only 160 cases of primary small cell carcinoma of the larynx have been reported worldwide.

Aim:
To report a rare case of small cell carcinoma of the larynx, in a 54-year-old man, including diagnostic work-up, and treatment with chemotherapy (CHT) and radiotherapy (RT), [47TD$DIF]compromised by the patient's nonadherence, and to spread awareness of the need of further research, focused on new therapeutic strategies, in patients with ESCCNET.

Case study:
The patient underwent induction CHT based on cisplatin and etoposide. Partial remissionwas obtained after the 3rd cycle of CHT, confirmed by the CT scan. The patient refused further CHT. He underwent RT. The residual larynx tumor and elective nodal volume were irradiated. A follow-up laryngological examination and control CT scan, performed two months after the completion of RT, showed a complete remission. Eight months later brain CT revealed multiple metastases. Palliative cranial irradiation and CHT were applied. The patient died in October 2011.

Results and discussion:
ESCCNET, an unusual neoplasm, accounting for 0.5% of all laryngeal carcinomas, is most commonly located in the supraglottic region. In contrast to squamous cell carcinoma of the larynx, a single modality therapy is not advised for ESCCNET, because these tumors are biologically aggressive, and at least 73% of patients have distant metastases. Therefore, RT and CHT in concomitant or sequential fashion offer the best chance of survival. However, in the presented case, the recommended therapy was not fully implemented, due to the patient's noncompliance.

Conclusions:
This report underscores the need for thorough, systemic diagnostic work-up, and emphasizes that the combination of RT and CHT remains the treatment of choice for ESCCNET (while surgery is reserved for persistent and recurrent disease). In addition, it points out that the new therapeutic strategies to improve survival in ESCCNET are needed, such as a prophylactic cranial irradiation that could be explored in future clinical trials.

CONFLICT OF INTEREST
None declared.
REFERENCES (16)
1.
Barnes L. Neuroendocrine tumors. In: Barnes L, Eveson JW, Reichart P, Sidransky D, eds. Pathology and Genetics of Head and Neck Tumors. WHO Classification of Tumors. Lyon: IARC Press; 2005:135–139.
 
2.
Lu CH, Chou WC, Chen CC, Lin JT, Chan CH, Lee KD. Extrapulmonary small cell carcinoma: a review. J Intern Med Taiwan. 2009;20:294–300.
 
3.
Olofsson J, van Nostrand AWP. Anaplatic small cell carcinoma of larynx. Case report. Ann Otol Rhinol Laryngol. 1972;81(2):284–287.
 
4.
Ferlito A, Silver CE, Bradford CR, Rinaldo A. Neuroendocrine neoplasms of the larynx: an overview. Head Neck. 2009;31(12):1634–1646.
 
5.
Aggarwal G, Jackson L, Sharma S. Primary combined small cell carcinoma of larynx with lateralized histologic components and corresponding side specific neck nodal metastasis: report of a unique case and review of literature. Int J Clin Exp Pathol. 2011;4(1):111–117.
 
6.
Jaiswal VR, Hoang MP. Primary combined squamous and small cell carcinoma of the larynx: a case report and review of the literature. Arch Pathol Lab Med. 2004;128(11):1279–1282.
 
7.
Ferlito A, Rinaldo A. Small cell neuroendocrine carcinoma of the larynx: a preventable and frustrating disease with a highly aggressive lethal behavior. ORL J Otorhinolaryngol Relat Spec. 2003;65(3):131–133.
 
8.
Monroe AT, Morris CG, Lee E, Mendenhall WM. Small cell carcinoma of the head and neck: the University of Florida experience. J HK Coll Radiol. 2005;8:83–86.
 
9.
Myers TJ, Kessimian N. Small cell carcinoma of the larynx and ectopic antidiuretic hormone secretion. Otolaryngol Head Neck Surg. 1995;113(3):301–304.
 
10.
HatoumGF, Patton B, Takita C, et al. Small cell carcinoma of the head and neck: the university of Miami experience. Int J Radiat Oncol Biol Phys. 2009;74(2):477–481.
 
11.
Dams A, Kibiłda B. Small cell neuroendocrine carcinoma of the larynx—a case report. Otolaryngol Pol. 2009;63(3)283–286 [in Polish].
 
12.
Gaba A, Mbaoma R, Breining D, Smith RV, Beitler JJ, Haigentz Jr. MJr.. Unusual sites of malignancies: CASE 1: Small-cell carcinoma of the hypopharynx. J Clin Oncol. 2005;23(9):2094–2096.
 
13.
Haider K, Shahid RK, Finch D, et al. Extrapulmonary small cell carcinoma: a Canadian province's experience. Cancer. 2006;107(9):2262–2269.
 
14.
Lin YL, Chung CY, Chang CS, et al. Prognostic factors in extrapulmonary small cell carcinoma: a large retrospective study. Oncology. 2007;72(3–4):181–187.
 
15.
Baugh RF,Wolf GT, Beals TF, Krause CJ, Forastiere A. Small cell carcinoma of the larynx: results of therapy. Laryngoscope. 1986;96(11):1283–1290.
 
16.
Singh H, Chauhan A. Primary Small Cell Carcinoma of the Larynx: Report of a Rare Tumor. http://www.hindawi.com/journal.... Accessed 03.06.16.
 
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