Results 71 to 80 of about 5,962 (164)

Colonic Ganglioneuroma—A Rare Finding During Colonoscopy

open access: yesDiagnostics
A 66-year-old female underwent a colonoscopy for persistent left lower abdominal discomfort and mucous stool passage. Endoscopic examination revealed a 3 mm sessile polyp in the ascending colon. Histopathological examination of the polyp showed preserved
Anita Sejben, Tamás Lantos
doaj   +1 more source

RET codon 618 mutations in Saudi families with multiple endocrine neoplasia Type 2A and familial medullary thyroid carcinoma

open access: yesAnnals of Saudi Medicine, 2013
BACKGROUND AND OBJECTIVES: Certain diseases such as multiple endocrine neoplasia (MEN) 2A, MEN 2B, familial and sporadic medullary thyroid carcinoma (MTC) and renal dysgenesis are related to abnormalities of the RET protein.
Faiza Qari
doaj   +1 more source

Integrative analysis of neuroblastoma and pheochromocytoma genomics data

open access: yesBMC Medical Genomics, 2012
Background Pheochromocytoma and neuroblastoma are the most common neural crest-derived tumors in adults and children, respectively. We have performed a large-scale in silico analysis of altogether 1784 neuroblastoma and 531 pheochromocytoma samples to ...
Szabó Peter M   +7 more
doaj   +1 more source

Abstracts

open access: yesMolecular Oncology, Volume 20, Issue S1, Page 1-692, August 2026.
Abstracts submitted to the ‘EACR 2026 Congress: Innovative Cancer Science’, from 08–11 June 2026 and accepted by the Congress Organising Committee are published in this Supplement of Molecular Oncology, an affiliated journal of the European Association for Cancer Research (EACR).
wiley   +1 more source

Persistent Hiccups—An Unusual Presentation of Bilateral Pheochromocytoma without Syndromic Association: A Case Report

open access: yesCase Reports in Endocrinology, 2012
Pheochromocytoma is a rare catecholamine-producing tumor arising from chromaffin tissue in the adrenal medulla, occurring in less than 0.2 percent of patients with hypertension. The mean age at diagnosis is about 40 years.
Nitin Aherrao   +6 more
doaj   +1 more source

Neoplasias endocrinas múltiples: de lo molecular a lo clínico

open access: yesRevista Médica Clínica Las Condes
Resumen: Las neoplasias endocrinas múltiples (NEM) tipo 1, 2 (se subdivide en 2A y 2B), 4 y 5; constituyen síndromes genéticos hereditarios con un patrón de transmisión autosómico dominante.
Nelson Wohllk, MD, Consuelo Olave, MD
doaj   +1 more source

Non-Syndromic Ganglioneuromatosis of the Gallbladder, an Extremely Rare Condition: Case Report and Literature Review

open access: yesReports
Background and Clinical Significance: Ganglioneuromatosis is a benign proliferation of mature ganglion cells, Schwann cells, and nerve fibers within the enteric or autonomic nervous system.
Catalin-Bogdan Satala   +3 more
doaj   +1 more source

A Case Series Study of Solitary Mucosal Neuroma-Rare Cases of Benign Peripheral Neurogenic Tumours

open access: yesClinical Pathology
Aim/objective: Mucosal neuroma (MN) is a benign peripheral nerve tumour that usually occurs as a symptom of multiple endocrine neoplasia type 2B (MEN2B) (MEN2B-associated MN). MN that is not associated with MEN2B is termed solitary mucosal neuroma (SMN).
Yu Takayama   +8 more
doaj   +1 more source

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