Rare cases of head and neck’s neuroendocrine carcinomas disease: Case series of 4 patients and review of the literature

Autor: Sami Rouadi, Reda Abada, Rabii Laababsi, Bushra Abdulhakeem, Anas Bouzbouz, Mohamed Roubal, Mohamed Mahtar
Jazyk: angličtina
Rok vydání: 2019
Předmět:
Larynx
Nasal cavity
medicine.medical_specialty
S
Surgery

NE
neuroendocrine

LAC
laryngeal atypical carcinoid

medicine.medical_treatment
RT
radiotherapy

Article
ANED
alive no evidence of disease

Metastasis
OS
overall survival

03 medical and health sciences
0302 clinical medicine
AC
atypical carcinoid

Paraganglioma
medicine
CRT
chemo radiotherapy

Chemotherapy
Case series
Lymph node
DOD
died of disease

Head and neck carcinoma
AWD
alive with disease

Radiotherapy
business.industry
ca
carcinoma

mon
months

medicine.disease
TC
typical carcinoid

post-op
post-operative

D
death from other causes

FU
follow up

Tonsillectomy
Radiation therapy
medicine.anatomical_structure
030220 oncology & carcinogenesis
Tonsil
Neuroendocrine carcinoma
030211 gastroenterology & hepatology
Surgery
Radiology
SmCC
small cell neuroendocrine carcinoma

business
LCNEC
large cell neuroendocrine carcinomas

CT
chemotherapy

n/s
not specified
Zdroj: International Journal of Surgery Case Reports
ISSN: 2210-2612
Popis: Highlights • Cervical lymph node SmCC as a primary tumor’s location, was never described in the literature according to what we know. • AC neuroendocrine carcinoma of the tonsil has never been described in the literature up to our knowledge. • A review of the literature was performed, indicating treatment and disease’s prognosis. • In 2012, the 2005 WHO classification of neuroendocrine tumors of the head and neck region was modified by adding the ranges of the Ki-67 and suggested that LCNEC should be considered a distinct disease entity and be separated from AC.
Introduction Primary neuroendocrine carcinomas are uncommon head and neck malignancies. Their classification is still debated. We report four cases of unusual primary locations of neuroendocrine carcinomas of head and neck region emphasizing two entities and rare sites that were never described in the literature to the best of our knowledge. Presentation of cases We reported four different cases of neuroendocrine carcinomas (nasal cavity, larynx, lymph nodes and tonsil) treated in our institution. The diagnosis was made by biopsy and confirmed by Immunohistochemical study. We underscored 2 atypical and rare entities in their location and anatomo histopathological type. Chemotherapy and radiotherapy were proposed for patients with nasal’s and laryngeal locations. This latter had also undergone surgery. For lymph node location, the patient received decompressive radiotherapy alone. The patient diagnosed with neuroendocrine carcinoma of the tonsil didn’t get any treatment except initial tonsillectomy for diagnosis purposes. Regarding the evolution in our case series, 2 patients had a relapse with local and regional metastasis. Among the 4 patients, 50 % passed away, one is still alive with deterioration of his general status and one is lost to follow-up and refused undergoing further investigations. Discussion There is confusion in the literature regarding the classification of neuroendocrine carcinomas. According to the 2005 WHO, these lesions, can be subdivided into TC, AC (including LCNEC), SmCC, combined SmCC with nonsmall cell carcinoma, and paraganglioma. Their treatment is still debated. Through an overview of the literature, we have gathered the main studies and 2 meta-analysis summarizing the mainstay treatment and disease’s outcome. Conclusion Neuroendocrine carcinomas of head and neck region are aggressive tumors with poor prognosis, low incidence and their diagnosis is not obvious. The treatment protocol depends on the type, the site of the lesions, and metastasis status. It’s still not well codified.
Databáze: OpenAIRE