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Pulmonary invasive mucinous adenocarcinoma

open access: yesHistopathology, 2023
Invasive mucinous adenocarcinoma (IMA) is a relatively rare subtype of lung adenocarcinoma, composed of goblet and/or columnar tumour cells containing abundant intracytoplasmic mucin vacuoles. While a majority of IMAs are driven by KRAS mutations, recent studies have identified distinct genomic alterations, such as NRG1 and ERBB2 fusions.
Wei‐Chin Chang   +2 more
openaire   +3 more sources

Mucinous colorectal adenocarcinoma: clinical pathology and treatment options

open access: yesCancer Communications, 2019
Mucinous colorectal adenocarcinoma is a distinct subtype of colorectal cancer (CRC) characterized by the presence of abundant extracellular mucin which accounts for at least 50% of the tumor volume.
Cong Luo, Shuyi Cen, Guojun Ding, Wei Wu
doaj   +2 more sources

Case of mucinous adenocarcinoma of the lung associated with congenital pulmonary airway malformation in a neonate [PDF]

open access: yesKorean Journal of Pediatrics, 2018
Congenital pulmonary airway malformation (CPAM), previously known as congenital cystic adenomatoid malformation, is a rare developmental lung abnormality associated with rhabdomyosarcoma, pleuropulmonary blastoma, and mucinous adenocarcinoma of the lung.
Juneyoug Koh   +6 more
doaj   +2 more sources

Mucinous ovarian neoplasm – outcomes of a rare tumor [PDF]

open access: yesGynecologic Oncology Reports
Background: Mucinous epithelial ovarian (mEO) tumors are rare entities. In this study, we describe the management and outcomes of patients treated for mucinous borderline tumor and mucinous adenocarcinoma of the ovary.
Bahareh Hamedi   +6 more
doaj   +2 more sources

Intestinal differentiated mucinous adenocarcinoma of the endometrium with sporadic MSI high status: a case report

open access: yesDiagnostic Pathology, 2017
Background Intestinal differentiation of primary mucinous adenocarcinoma of the uterine corpus is exceedingly rare in comparison to the approximately 25% rate in endocervical and ovarian mucinous carcinoma. Additionally, little is known about the related
Mafalda Trippel   +8 more
doaj   +2 more sources

A case of Endometrioid endometrial adenocarcinoma with synchronous low-grade Appendiceal mucinous neoplasm and Pseudomyxoma peritonei

open access: yesJournal of Minimal Access Surgery, 2021
Pseudomyxoma peritonei (PMP) is a rare condition usually associated with ruptured low-grade mucinous neoplasm of the appendix. Rarely, PMP can originate from mucinous adenocarcinoma of the ovary.
Shweta Raje, Sharda Arvind, Gayatri Rao
doaj   +1 more source

Epidemiology of Mucinous Adenocarcinomas [PDF]

open access: yesCancers, 2020
Mucinous (colloid) adenocarcinomas (MAs) are a rare histological subtype of adenocarcinomas where extracellular mucin comprises more than 50% of the tumor. Most literature on MAs relate to cancers from colorectal and breast sites; however, the literature lacks a standardized overview of the MA disease entity. Particularly in colorectal cancer, some MAs
Matthew G. K. Benesch   +1 more
openaire   +2 more sources

Efficacy of Systemic Chemotherapy in Patients With Low-grade Mucinous Appendiceal Adenocarcinoma

open access: yesJAMA Network Open, 2023
Key Points Question Is fluoropyrimidine-based systemic chemotherapy effective in treating patients with inoperable low-grade mucinous appendiceal adenocarcinoma?
J. Shen   +19 more
semanticscholar   +1 more source

Positive response to niraparib in chemo-refractory patients with metastatic appendiceal mucinous adenocarcinoma harboring ATM mutations: A case report

open access: yesFrontiers in Oncology, 2023
BackgroundAppendiceal mucinous adenocarcinoma, one kind of specific colorectal cancer, is lowly prevalent and rarely diagnosed in clinical practice.
Junhui Wang   +3 more
doaj   +1 more source

Perianal mucinous adenocarcinoma [PDF]

open access: yesCancer, 1977
Perianal mucinous adenocarcinoma, also known as anal duct or anal gland carcinoma, is a rare tumor usually associated with chronic fistulae-in-ano. Whether the tumor occurs primarily and the fistula is a secondary manifestation, or whether this tumor arises in a chronic fistulous tract is debatable. Diagnosis can be made only by open deep biopsy of the
P G, Prioleau, M S, Allen, T, Roberts
openaire   +2 more sources

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