Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature

Head and neck tumors account for roughly 3% of malignancies in the United States and about 90% of these tumors are squamous cell cancers. Neuroendocrine neoplasms arise from neural crest cells and are commonly found in the gastrointestinal tract. Neuroendocrine neoplasms arising from the head and ne...

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Main Authors: Stephanie Niforatos MD, Michael Sandhu MD, Mansi Kallem MD, Serenella Serinelli MD, PhD, Christopher Curtiss MD, Komal Akhtar MD
Format: Article
Language:English
Published: SAGE Publishing 2022-09-01
Series:Journal of Investigative Medicine High Impact Case Reports
Online Access:https://doi.org/10.1177/23247096221127792
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author Stephanie Niforatos MD
Michael Sandhu MD
Mansi Kallem MD
Serenella Serinelli MD, PhD
Christopher Curtiss MD
Komal Akhtar MD
author_facet Stephanie Niforatos MD
Michael Sandhu MD
Mansi Kallem MD
Serenella Serinelli MD, PhD
Christopher Curtiss MD
Komal Akhtar MD
author_sort Stephanie Niforatos MD
collection DOAJ
description Head and neck tumors account for roughly 3% of malignancies in the United States and about 90% of these tumors are squamous cell cancers. Neuroendocrine neoplasms arise from neural crest cells and are commonly found in the gastrointestinal tract. Neuroendocrine neoplasms arising from the head and neck tend to be rare. In this article, we present a rare case of human papilloma virus–associated poorly differentiated small cell neuroendocrine carcinoma (NEC). Our patient was a 62-year-old African American man who presented with worsening left-sided neck pain and swelling that started 3 months prior to presentation, associated with an unintentional 20-pound weight loss over 6 months, hoarseness in his voice, in addition to dysphagia and odynophagia. Biopsy of left-sided tongue mass revealed poorly differentiated small cell NEC that was positive for HPV (E6/E7) RNA in situ hybridization. Patient was found to have metastatic disease at the time of diagnosis and given the aggressive nature of small cell NECs and the patient’s symptomatic burden, chemotherapy with cisplatin and etoposide was initiated in the hospital. The patient was subsequently discharged from the hospital and is continuing treatment outpatient with cisplatin, etoposide, and atezolizumab.
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spelling doaj.art-c92f524992534d85a13a854c74f677fc2022-12-22T01:59:57ZengSAGE PublishingJournal of Investigative Medicine High Impact Case Reports2324-70962022-09-011010.1177/23247096221127792Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the LiteratureStephanie Niforatos MD0Michael Sandhu MD1Mansi Kallem MD2Serenella Serinelli MD, PhD3Christopher Curtiss MD4Komal Akhtar MD5State University of New York Upstate Medical University, Syracuse, USAState University of New York Upstate Medical University, Syracuse, USAState University of New York Upstate Medical University, Syracuse, USAState University of New York Upstate Medical University, Syracuse, USAState University of New York Upstate Medical University, Syracuse, USAState University of New York Upstate Medical University, Syracuse, USAHead and neck tumors account for roughly 3% of malignancies in the United States and about 90% of these tumors are squamous cell cancers. Neuroendocrine neoplasms arise from neural crest cells and are commonly found in the gastrointestinal tract. Neuroendocrine neoplasms arising from the head and neck tend to be rare. In this article, we present a rare case of human papilloma virus–associated poorly differentiated small cell neuroendocrine carcinoma (NEC). Our patient was a 62-year-old African American man who presented with worsening left-sided neck pain and swelling that started 3 months prior to presentation, associated with an unintentional 20-pound weight loss over 6 months, hoarseness in his voice, in addition to dysphagia and odynophagia. Biopsy of left-sided tongue mass revealed poorly differentiated small cell NEC that was positive for HPV (E6/E7) RNA in situ hybridization. Patient was found to have metastatic disease at the time of diagnosis and given the aggressive nature of small cell NECs and the patient’s symptomatic burden, chemotherapy with cisplatin and etoposide was initiated in the hospital. The patient was subsequently discharged from the hospital and is continuing treatment outpatient with cisplatin, etoposide, and atezolizumab.https://doi.org/10.1177/23247096221127792
spellingShingle Stephanie Niforatos MD
Michael Sandhu MD
Mansi Kallem MD
Serenella Serinelli MD, PhD
Christopher Curtiss MD
Komal Akhtar MD
Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
Journal of Investigative Medicine High Impact Case Reports
title Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
title_full Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
title_fullStr Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
title_full_unstemmed Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
title_short Small Cell Neuroendocrine of the Head and Neck: A Rare Presentation and Review of the Literature
title_sort small cell neuroendocrine of the head and neck a rare presentation and review of the literature
url https://doi.org/10.1177/23247096221127792
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