Results 61 to 70 of about 4,917,419 (163)

Combined classical carcinoid and goblet cell carcinoid tumor: a new morphologic variant of carcinoid tumor of the appendix

open access: yes, 2010
Carcinoid tumors are the most common neoplasms of the appendix. Histologically they have been categorized as classical, tubular, or goblet cell types. Goblet cell carcinoid has been regarded as a distinctive tumor type, not related to classic carcinoids,
Albores-Saavedra, J   +12 more
core   +1 more source

Goblet Cell Carcinoid of the appendix: a 52 years old male with acute appendicitis

open access: yes, 2007
Goblet cell carcinoid, also variably known as adenocarcinoid, mucinous carcinoid, and crypt cell carcinoma, is a rare neoplasm with distinct histological and clinical features.
Trujillo Vilchez,R.   +6 more
core   +1 more source

Tumor-to-tumor metastasis from appendiceal adenocarcinoma to an ovarian mature teratoma, mimicking malignant transformation of a teratoma: a case report

open access: yesDiagnostic Pathology, 2019
Background Tumor-to-tumor metastasis (TTM) is a rare but well-documented phenomenon that is defined as metastasis in a histologically distinct tumor. Ovarian mature teratomas (OMTs) can coexist with various cancers by malignant transformation, which may ...
Mitsutake Yano   +6 more
doaj   +1 more source

E‐selectin affinity glycoproteomics reveals neuroendocrine proteins and the secretin receptor as a poor‐prognosis signature in colorectal cancer

open access: yesMolecular Oncology, Volume 19, Issue 3, Page 635-658, March 2025.
Screening colorectal tumors for glycoproteins linked to disease progression has revealed several potential therapeutic targets. The secretin receptor (SCTR), identified as a marker of poor prognosis and metastasis in colorectal cancer, has been shown to be a key carrier of N‐glycans with sialylated Lewis antigens. These cancer‐specific glycoproteoforms
Sofia Cotton   +12 more
wiley   +1 more source

Goblet cell carcinoid of the appendix: a case report [PDF]

open access: yesTurkish Journal of Pathology, 2014
Goblet cell carcinoid of the appendix is a rare neuoroendocrine tumor that possesses histological features of both adenocarcinoma and neuoroendocrine tumor. Goblet cell carcinoid of the appendix is more aggressive than conventional neuroendocrine tumors. Here we report a case of a 54-year-old woman with goblet cell carcinoid tumor in the appendix.
Dudu Solakoğlu, Kahraman, Niyazi, Akin
openaire   +2 more sources

Mixed Goblet Cell Carcinoid-Adenocarcinoma: A Case Series [PDF]

open access: yes, 2017
INTRODUCTION: Mixed goblet cell carcinoid-adenocarcinoma (GCC) tumors are a group of rare heterogenous neoplasms of the appendix accounting for \u3c 5% of all primary appendiceal tumors. They are characterized as an intermediate between classic carcinoid
Espinosa, Jairo, M.D.   +5 more
core   +1 more source

Adenocarcinoma Ex–Goblet Cell Carcinoid of the Appendix With Metastatic Peritoneal Spread to Meckel’s Diverticulum and Endometriosis

open access: yes, 2017
Adenocarcinoma ex–goblet cell carcinoid is a very rare and histologically unique appendiceal malignancy with dual glandular and neuroendocrine differentiation.
Grace Y. Lin   +3 more
core   +1 more source

Integrated omics revealed the altered colonic microenvironment after inhibition of peripheral serotonin synthesis by LP533401

open access: yesiMetaOmics, Volume 1, Issue 2, December 2024.
The colonic microenvironment of neonatal rats was altered after administration of the peripheral 5‐hydroxytryptamine (5‐HT) inhibitor LP533401, resulting in increased crypt depth and decreased myenteric thickness. Multi‐omics approaches, including metagenomics, transcriptomics, and metabolomics, in combination with immunofluorescence, were employed to ...
Yidan Ling   +5 more
wiley   +1 more source

Incidental Finding of Goblet Cell Adenocarcinoma Post Appendectomy: A Rare Case Report

open access: yesDubai Medical Journal
Introduction: One of the most frequent etiologies of an acute abdomen is appendicitis, which ranks as one of the primary reasons for surgical emergencies globally.
Fathima Hana Mohamed Naushad   +2 more
doaj   +1 more source

Clinicopathological and epigenetic differences between primary neuroendocrine tumors and neuroendocrine metastases in the ovary

open access: yesThe Journal of Pathology: Clinical Research, Volume 10, Issue 6, November 2024.
Abstract Currently, the available literature provides insufficient support to differentiate between primary ovarian neuroendocrine tumors (PON) and neuroendocrine ovarian metastases (NOM) in patients. For this reason, patients with a well‐differentiated ovarian neuroendocrine tumor (NET) were identified through electronic patient records and a ...
Merijn CF Mulders   +8 more
wiley   +1 more source

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