Results 91 to 100 of about 7,577 (194)

COMBINED METHODS OF TREATMENT THE CONGENITAL ARTERIO-VENOUS FISTULAS OF PERIPHERAL VESSELS

open access: yesВестник хирургии имени И.И. Грекова, 2018
A 10-year experience and results of combined methods of surgical treatment of arterio-venous fistulas of peripheral vessels in 50 patients were analyzed.
A. D. Gaibov   +3 more
doaj   +1 more source

Hypertensive portal colopathy in schistosomiasis mansoni: proposal for a classification

open access: yesMemorias do Instituto Oswaldo Cruz, 2004
Portal hypertension is a frequent complication of chronic liver disease, detected not only in schistosomiasis, but also in cirrhosis of any etiology. Vascular alterations in the colonic mucosa are a potential source for acute or chronic bleeding and have
Maria Angelina C Miranda   +6 more
doaj   +1 more source

Anaphylactic Transfusion Reaction to Washed Packed Red Blood Cells (pRBCs)

open access: yesCase Reports in Critical Care, Volume 2026, Issue 1, 2026.
The annual blood transfusions in the United States exceed 16 million units, and 1% of the cases experience adverse events. Febrile nonhemolytic transfusion reaction is most common accounting for 1%–3% of the cases. Anaphylactic transfusion reaction accounts for 0.00002% of the units transfused.
Schaza Javed Rana   +4 more
wiley   +1 more source

Push enteroscopy in management of suspected small bowel diseases: Is it still needed?

open access: yesJournal of Digestive Endoscopy, 2014
Background and Study Aims: Small intestinal lesions still represent a challenge in diagnosis and treatment. The detection of small bowel lesions has been difficult due to limited visualization of the small bowel by esophagogastroduodenoscopy (EGD) and ...
Mohamed A. Tawfik, Abd Allah El-Sawy
doaj   +1 more source

Endoscopic Management of Jejunal Diverticular Bleeding: A Case Report and Systematic Review of the Literature

open access: yesCase Reports in Gastrointestinal Medicine, Volume 2026, Issue 1, 2026.
Bleeding from a jejunal diverticulum is a rare and potentially severe condition, challenging both to diagnose and to treat. We report the case of a 56‐year‐old woman presenting with massive melena, who initially underwent esophagogastroduodenoscopy (EGD) and abdominal angio‐CT, both unable to identify the bleeding source.
Marta Pettinelli   +8 more
wiley   +1 more source

“Hughes‐Stovin Syndrome: A Comprehensive Narrative Review”

open access: yesHealth Science Reports, Volume 8, Issue 11, November 2025.
ABSTRACT Background and Aims Hughes‐Stovin Syndrome (HSS) is an extremely rare vasculitic disorder characterized by a combination of pulmonary artery aneurysms and deep venous thrombosis (DVT). Often considered a variant or incomplete form of Behçet's disease (BD), it presents diagnostic and therapeutic challenges due to its overlap with other ...
Muhammad Mustafa Imran   +11 more
wiley   +1 more source

Capsule Endoscopy in Elderly Patients with Obscure Gastrointestinal Bleeding: Retrospective Analysis of 152 Cases

open access: yesInternational Journal of Gerontology, 2010
Background: Capsule endoscopy (CE) is a highly sensitive examination for the detection of small bowel lesions. However, there are few clinical studies on obscure gastrointestinal bleeding (OGIB) among elderly patients. This study reports the risk factors
Li-Rung Shyung   +6 more
doaj   +1 more source

Angiodysplasia of the colon

open access: yes, 1979
Angiodysplasia of the colon was diagnosed by arteriography in 33 patients. Approximately one fourth of the lesions were located in the left side of the colon. Three patients with sigmoid lesions had a second lesion elsewhere in the gastrointestinal tract.
Tutton, R.H.   +3 more
core  

Gastrointestinal angiodysplasia in three Saudi children.

open access: yes, 2009
Angiodysplasia is a term used to describe distinct gastrointestinal mucosal ectasias that are not associated with cutaneous lesions, systemic vascular disease or a familial syndrome.
Alnassar Saleh   +5 more
core   +1 more source

Gastric angiodysplasia in a hereditary hemorrhagic telangiectasia type 2 patient [PDF]

open access: yes, 2012
Hereditary hemorrhagic telangiectasia (HHT) is a rare autosomal-dominantly inherited disease that occurs in approximately one in 5000 to 8000 people. Clinical diagnosis of HHT is made when a person presents three of the following four criteria: family ...
Kwon, Kwang An   +7 more
core   +1 more source

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