Results 1 to 10 of about 10,023,096 (196)

Primary Small Cell Neuroendocrine Carcinoma of the Endometrium [PDF]

open access: yesCase Reports in Oncology, 2012
Background: Small cell neuroendocrine carcinoma is very rarely encountered within the endometrium. Case Study: A patient underwent a hysterectomy and salpingo-oophorectomy for a suspicious gynecologic condition.
Lisa N. Abaid   +3 more
doaj   +4 more sources

Mediastinum primary small cell neuroendocrine carcinoma

open access: yesContemporary Oncology, 2016
Neuroendocrine carcinoma, which was first reported in 1907, is a rare disease [1]. This cancer most commonly originates in the gastrointestinal tract, although it can occur in the lungs, thymus, parathyroid gland, ovaries, and biliary system. However, mediastinal primary small cell neuroendocrine carcinoma (MPSCN) is extremely rare.
Hong-Lu Wang   +3 more
doaj   +4 more sources

Case Report: Analysis of colposcopic image features in a case of early-stage small cell neuroendocrine carcinoma of the cervix [PDF]

open access: yesFrontiers in Oncology
This study analyzes the colposcopy findings of an early-stage cervical small cell neuroendocrine carcinoma with ectopic kidney in a patient treated at Fuyang Peoples Hospital in October 2023.
Leilei Yuan, Kejie Liu
doaj   +2 more sources

Prevalence, Associated Factors, and Survival Outcomes of Small-Cell Neuroendocrine Carcinoma of the Gynecologic Tract: A Large Population-Based Analysis

open access: yesFrontiers in Medicine, 2022
Small-cell carcinomas are highly malignant tumors with neuroendocrine function and which often occur in the lungs. Primary small-cell neuroendocrine carcinomas of the gynecologic tract are extremely rare.
Li Pang, Shizhuo Wang
doaj   +1 more source

Mixed endocervical adenocarcinoma and high-grade neuroendocrine carcinoma of the cervix: A case report

open access: yesIndian Journal of Pathology and Microbiology, 2021
Adenocarcinoma admixed with neuroendocrine carcinoma of the uterine cervix is a rare malignancy with a poor prognosis. In the literature, there are few reported cases.
Gizem Teoman, Safak Ersoz
doaj   +1 more source

Vulvar neuroendocrine carcinoma that is independent of merkel cell polyomavirus and human papillomavirus suggests endometrial cancer recurrence: a case report

open access: yesBMC Endocrine Disorders, 2022
Background Vulvar neuroendocrine carcinomas with small cell morphology need an appropriate differential diagnosis with respect to primary Merkel cell carcinomas, primary small cell neuroendocrine carcinomas, and secondary/metastatic carcinomas.
Tomoko Hirakawa   +4 more
doaj   +1 more source

Metastatic neuroendocrine carcinoma to the mandibular gingiva from the duodenum papilla

open access: yesOral Oncology Reports, 2023
Neuroendocrine carcinoma is a high-grade carcinoma with morphological and immunohistochemical features of neuroendocrine differentiation. Poorly differentiated neuroendocrine carcinoma which has two subtypes (small cell or large cell type) is extremely ...
Toshinori Iwai   +3 more
doaj   +1 more source

Two additional cases of parotid neuroendocrine carcinoma: Is there a wall that cannot be overcome in the cellular morphology?

open access: yesHuman Pathology Reports, 2022
Herein, we summarize two rare cases of salivary neuroendocrine carcinoma arising in the parotid gland. The patients were a 54-year-old Japanese female and a 74-year-old Japanese male.
Hiroshi Harada   +6 more
doaj   +1 more source

Primary large-cell neuroendocrine carcinoma of the prostate [PDF]

open access: yesArchives of the Balkan Medical Union, 2022
Introduction. Depending on neuroendocrine differentiation, the prostate cancer is divided into two major groups: primary neuroendocrine prostate tumour (carcinoid, small-cell, and large-cell neuroendocrine carcinoma) or as a focal tumour in conventional ...
Spasimir T. SHOPOV
doaj   +1 more source

THE PROGNOSIS OF THE DIFFERENT ESOPHAGEAL NEUROENDOCRINE CARCINOMA SUBTYPES: A POPULATION-BASED STUDY

open access: yesArquivos de Gastroenterologia, 2022
Background Neuroendocrine neoplasms are extremely rare and account for 0.4% to 2% of all malignant esophageal neoplasms. The burden of the neuroendocrine histological type on the patients’ prognosis and survival is poorly debated.
Francisco TUSTUMI   +5 more
doaj   +1 more source

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