Results 111 to 120 of about 95,682 (200)

A Novel GDF2 Mutation in a Patient With Hereditary Hemorrhagic Telangiectasia Complicated by Acute Cerebral Infarction

eJHaem, Volume 7, Issue 5, October 2026.
ABSTRACT Introduction Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant disease and the growth differentiation factor 2 (GDF2) variants have been identified as an infrequent cause of HHT. Case Report We report a 64‐year‐old female patient with an onset of ischemic stroke suspected related with microscopic pulmonary arteriovenous ...
Huaqin Zuo, Lingling Qian, Jian Jing, Lu Wang, Xiaobo Li, Yong Chen, Xuefeng Wang, Qiulan Ding, Jian Gu, Mei Sun   +9 more
wiley   +1 more source

Management of Absent Upper Esophageal Sphincter Opening After Neurological Injury

The Laryngoscope, Volume 136, Issue 10, Page 4383-4391, October 2026.
This study evaluated the effects of swallowing therapy and cricopharyngeus (CP) muscle surgery on upper esophageal sphincter (UES) opening, oral intake, and airway protection in patients with absent UES opening following neurological injury. CP‐targeted surgeries were associated with improved bolus passage and oral intake, but persistent aspiration ...
Radhika Rawat, Cyrus W. Abrahamson, Kelly Rogers, Jonelyn Langenstein, Jaymie Bromfield, Arjun Seth, James A. Burns, Andrew P. Stein   +7 more
wiley   +1 more source

Congenital Lung Malformations in Neonates: A 9‐Year Tunisian Cohort Highlighting Diagnostic Challenges and Outcomes in a Resource‐Limited Setting

Pediatric Pulmonology, Volume 61, Issue 10, October 2026.
ABSTRACT Background Congenital lung malformations (CLMs) represent a broad spectrum of developmental anomalies with highly variable prenatal and postnatal presentations and outcomes. Their postnatal management remains non‐standardized. This study aimed to describe the spectrum of bronchopulmonary malformations diagnosed in the neonatal period, assess ...
Hajer Chourou, Rim Ben Aziza, Wafa Belhadj Ammar, Cyrine Saadi, Maryem Marzouki, Youssef Hellal, Said Jlidi, Samia Kacem, Bilel Jerbi   +8 more
wiley   +1 more source

A Case of Platypnea‐Orthodeoxia Syndrome Caused by Patent Foramen Ovale, Accompanied by Dilated Ascending Aorta, Thoracic Kyphosis and Persistent Eustachian Valve

Respirology Case Reports, Volume 14, Issue 10, October 2026.
We present a case of platypnea‐orthodeoxia syndrome associated with patent foramen ovale in conjunction with a dilated horizontal aorta, thoracic kyphosis and persistent Eustachian valve. ABSTRACT We present a case of platypnea‐orthodeoxia syndrome (POS) associated with patent foramen ovale (PFO).
Ayaka Kishimoto, Tomohiro Namiki, Yudai Ogata, Hiroya Sunabe, Toshihide Inui, Hiroaki Ishikawa, Hiroko Watanabe, Chihiro Ohta, Ruriko Numata, Naoto Kawamatsu, Tomoko Machino‐Ohtsuka, Tomoya Hoshi, Tohru Sakamoto   +12 more
wiley   +1 more source

Capillary malformation-arteriovenous malformation and RASA1 mutations

, 2011
Capillary malformation–arteriovenous malformation (CM–AVM) is a subtype of CM that is inherited as an autosomal-dominant disorder. Patients typically have multiple small pinkish-reddish CMs, often with a halo.
Boon, Laurence M., Laurence M Boon, Revencu, Nicole, Vikkula, Miikka, Nicole Revencu, Miikka Vikkula   +5 more
core   +1 more source

Fat‐Containing Soft Tissue Lesions of the Limbs and Body Wall—A Pictorial Essay

Journal of Medical Imaging and Radiation Oncology, Volume 70, Issue 7, Page 657-666, October 2026.
ABSTRACT Lipomatous tumours are frequently encountered on imaging. The spectrum of lipomatous tumours ranges from simple lipomas, which can be monitored clinically, to high‐grade liposarcomas, which require timely, multidisciplinary management. The presence of fat within lesions may also be observed in non‐lipomatous tumours, as well as in a variety of
Kai‐Zheong Lim, Cathryn Hui
wiley   +1 more source

Framework for headache management in pediatric patients with stroke and cerebrovascular lesions: A narrative review

Headache: The Journal of Head and Face Pain, Volume 66, Issue 9, Page 2138-2155, October 2026.
Abstract Objective To present a practical, evidence‐based framework for the management of headache disorders in pediatric patients with prior stroke or underlying cerebral vascular lesions, with particular attention to safety and efficacy of pharmacologic and non‐pharmacologic therapies.
Allison C. Hyland, Samuel J. Belfer, Christine K. Fox, Samantha L. Irwin, Rachel Vassar, Ann Oh, Sruthi Ilangovan, Amy A. Gelfand   +7 more
wiley   +1 more source

Spinal Arteriovenous Malformation Associated With Schimmelpenning Syndrome: Case Report

, 2013
The authors report the presentation and management of a 13-year-old girl with Schimmelpenning syndrome, a rare neurocutaneous syndrome; this patient suffered hemorrhage of a spinal arteriovenous malformation.
Bristol, Ruth, Sean D. Lavine, Albuquerque, Felipe C., Felipe C. Albuquerque, Lavine, Sean D., Ruth Bristol, Crowley, R. Webster, Ducruet, Andrew F., Kaith K. Almefty, Almefty, Kaith K., R. Webster Crowley, Andrew F. Ducruet   +11 more
core   +1 more source

Clinical and Diagnostic Insights into Penile Angiolymphoid Hyperplasia with Eosinophilia Based on a Case and Analysis of Previous Literature

Skin Research and Technology, Volume 32, Issue 10, October 2026.
ABSTRACT Angiolymphoid hyperplasia with eosinophilia (ALHE) is a rare, benign vascular proliferation of unknown origin. It typically occurs in the head and neck region, but can occasionally manifest in unusual locations, such as the penis. Herein, we report a case of ALHE in a 46‐year‐old HIV‐infected male presenting with multiple pruritic whitish ...
Rievanda Ayu Natasya, Retno Hesty Maharani, Eva Krishna Sutedja, Hermin Aminah Usman, Hanifah Nurul Huda, Pati Aji Achdiat   +5 more
wiley   +1 more source

Differentiating systemic artery-to-pulmonary artery fistula from pulmonary arteriovenous malformation: A case report

Radiology Case Reports
This report describes a rare case of a systemic artery-to-pulmonary artery fistula initially misdiagnosed as a pulmonary arteriovenous malformation in a 64-year-old male with severe emphysema.
Hiroshi Baba, MD, Kazunori Fukasawa, MD, Hiroyuki Kawaguchi, MD, Hiromu Hidaka, MD, Yoshiki Asayama, MD, PhD   +4 more
doaj   +1 more source