Introduction: Neuroendocrine tumours of the larynx are extremely rare, though they make up only 1% of tumours in this region with the most common site being the supraglottis. On exhaustive research on PubMed, there are only a few prior cases of neuroendocrine carcinoma of subglottis published in the literature.
Case Report: A 56-year-old male presented to our center with complaints of hoarseness and dyspnoea for 1 month which was insidious in onset and gradually progressive. The patient was evaluated and diagnosed with as subglottic mass. He underwent tracheostomy followed by Micro laryngoscopy and Biopsy under GA. Post-op HPE report s/o Neuroendocrine carcinoma- small cell type. On evaluation no second primary or distant metastatic site was identified.
Conclusion: Small cell neuroendocrine carcinoma of the subglottic larynx is an exceptionally rare and aggressive malignancy. Its presentation can be atypical, such as with symptoms of stridor, necessitating a high index of clinical suspicion. Early diagnosis and prompt, aggressive management are critical for improving outcomes. Despite the limited prognosis associated with this type of cancer, the patient in this case has shown a favourable response to chemoradiotherapy. Continued monitoring is essential due to the high risk of recurrence and metastasis associated with this malignancy.
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http://dx.doi.org/10.1007/s12070-024-05125-5 | DOI Listing |
Indian J Otolaryngol Head Neck Surg
January 2025
Department of Otolaryngology, Command Hospital (EC), Kolkata, India.
Introduction: Neuroendocrine tumours of the larynx are extremely rare, though they make up only 1% of tumours in this region with the most common site being the supraglottis. On exhaustive research on PubMed, there are only a few prior cases of neuroendocrine carcinoma of subglottis published in the literature.
Case Report: A 56-year-old male presented to our center with complaints of hoarseness and dyspnoea for 1 month which was insidious in onset and gradually progressive.
Front Endocrinol (Lausanne)
February 2025
Department of Pediatric Hematology and Oncology, Charles University, 2nd Faculty of Medicine and University Hospital Motol, Prague, Czechia.
Oncologist
March 2025
Department of Oncology, Taipei Veterans General Hospital, Taipei 11217, Taiwan.
Background: Neuroendocrine carcinoma (NEC) is an aggressive, poorly differentiated Grade 3 (G3) tumor with high nuclear and cellular atypia and Ki-67 indices over 20%. While most cases are lung NECs, extrapulmonary NECs are rarer and less studied. Standard treatment involves etoposide and platinum (EP) chemotherapy.
View Article and Find Full Text PDFMol Cancer Res
March 2025
University of Nebraska Medical Center, Omaha, NE, United States.
Small-cell lung carcinoma (SCLC) tumors are heterogeneous, with a subpopulation of cells primed for tumor initiation. Here, we show that Kinase Suppressor of Ras 2 (KSR2) promotes the self-renewal and clonogenicity of SCLC cells. KSR2 is a molecular scaffold that promotes Raf/MEK/ERK signaling.
View Article and Find Full Text PDFCancer Med
March 2025
Department of Urology, Urologic Surgery Center, Xinqiao Hospital, Third Military Medical University (Army Medical University), Chongqing, China.
Background: This study aimed to identify prognostic factors influencing survival in patients with bladder neuroendocrine carcinoma (NC).
Methods: This study utilized the Surveillance, Epidemiology, and End Results (SEER) database (2004-2015) to compare NC with urothelial carcinoma (UC). We evaluated the prognostic value of clinicopathological characteristics and survival outcomes for bladder NC patients.
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