Results 61 to 70 of about 44,864 (270)

Evaluation of radiological and clinical efficacy of ^{90}Y-DOTATATE} therapy in patients with progressive metastatic midgut neuroendocrine carcinomas [PDF]

open access: yes, 2009
Background: To evaluate the radiological and clinical therapeutic effectiveness of ^{90}Y-octreotate [DOTATATE] inpatients with progressive somatostatin receptor-positive midgut neuroendocrine carcinomas (GEPNETs).
Buscombe, John R.   +7 more
core  

Revisiting tricuspid regurgitation: Historical insights and emerging research perspectives

open access: yesEuropean Journal of Clinical Investigation, Volume 56, Issue 1, January 2026.
Tricuspid regurgitation (TR), once seen as benign, is now recognized as a serious and increasingly prevalent condition linked to aging and better imaging. Its association with greater morbidity and mortality has shifted clinical perspectives towards early diagnosis and intervention.
Claudia Gonzalez‐Cucharero   +5 more
wiley   +1 more source

Double Anti‐NMO and Anti‐MOG Positivity in a Patient With Metastatic Renal Carcinoma: First Reported Case

open access: yesCase Reports in Neurological Medicine, Volume 2026, Issue 1, 2026.
Background Neuromyelitis optica spectrum disorder (NMOSD) and myelin oligodendrocyte glycoprotein‐associated disease (MOGAD) are central nervous system (CNS) demyelinating disorders characterized by autoantibodies targeting aquaporin‐4 (AQP4) and MOG, respectively.
M. Fortanet García   +7 more
wiley   +1 more source

External beam irradiation of myocardial carcinoid metastases: a case report

open access: yesJournal of Medical Case Reports, 2007
The heart is an exceedingly rare site of metastatic involvement in carcinoid tumors. Only nineteen cases have been described in the literature over the past 30 years.
Strosberg Jonathan   +3 more
doaj   +1 more source

Thymic Neuroendocrine Tumor Presenting With Cervical Lymphadenopathy: A Case Report and Diagnostic Challenge

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
ABSTRACT Thymic neuroendocrine tumors are rare and may initially present with isolated cervical lymphadenopathy. Early recognition and a multidisciplinary diagnostic approach are crucial for timely identification, accurate localization, and curative resection.
Xiaohui Xie   +4 more
wiley   +1 more source

Carcinoid Heart Disease Associated with Primary Ovarian Carcinoid Tumor: A Rare Presentation

open access: yesHeart Views
Primary ovarian carcinoid tumors, an extremely rare subset of ovarian malignancies (
Rawaha Ahmad   +4 more
doaj   +1 more source

Pitfalls in the diagnosis of carcinoid syndrome

open access: yesFamily Medicine & Primary Care Review, 2016
Background . Carcinoid syndrome (CS ) is a rare syndrome, most commonly associated with neuroendocrine neoplasms (NEN s) of the small intestine. Carcinoid syndrome consists of diarrhea, vomiting, abdominal pain, cutaneous flushing, teleangiectasias ...
Dorota Kaczmarska-Turek   +8 more
doaj   +1 more source

An Unusual Case of Synchronous Carcinoid of Ovary and Gall Bladder [PDF]

open access: yes, 2013
Multifocal carcinoid is a known phenomenon. We present a rare combination of an ovarian carcinoid synchronous with gallbladder carcinoid. This rare combination has not been reported so far.
Nita Khurana   +3 more
core   +2 more sources

Tracheobronchial Aspergillosis Mimicking Pseudotumoral Lesions in a Rare Presentation of a Known Disease

open access: yesClinical Case Reports, Volume 13, Issue 12, December 2025.
Bronchoscopic view showing an obstructive tumor‐like lesion arising from the right main bronchus, consistent with tracheobronchial aspergillosis. ABSTRACT Tracheobronchial aspergillosis (TBA) is an uncommon form of invasive Aspergillus infection that can closely mimic endobronchial malignancy, particularly when presenting as an obstructive ...
Cinthya Castillo Gamboa   +3 more
wiley   +1 more source

A rare case of multiple endocrine neoplasia type 1 initially presenting as an asymptomatic, huge mediastinal mass: case report

open access: yesBMC Endocrine Disorders, 2021
Background Multiple endocrine neoplasia type 1 (MEN1) is a rare inherited syndrome that concurrently involves various endocrine glands. We report a rare case of MEN1 in a 43-year-old man whose first manifestation was an asymptomatic mediastinal mass ...
Ji Eun Jun   +4 more
doaj   +1 more source

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