Results 61 to 70 of about 13,125 (269)
Gastroduodenal Lipomatosis in Familial Multiple Lipomatosis [PDF]
Medical Principles and Practice, 2016 <b><i>Objective:</i></b> To present a case of gastroduodenal lipomatosis associated with familial multiple lipomatosis (FML). <b><i>Clinical Presentation and Intervention:</i></b> A 58-year-old male presented with FML that manifested as multiple, painless, subcutaneous lipomas on his body; his mother had ...
Aleksandra, Djuric-Stefanovic +3 more
openaire +2 more sources
Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes
Epilepsia Open, EarlyView.Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola +3 more
wiley +1 more source
Lipoleiomyoma of the Uterus [PDF]
, 2005 Lipoleiomyomas are uncommon benign neoplasms of uterus consisting of variable portions of mature lipocytes and smooth muscle cells. These tumours generally occur in asymptomatic obese perimenopausal or menopausal women.
Alper, Murat +4 more
core
A retrospective analysis of thyroid lesions containing mature adipose tissue [PDF]
, 2014 Objectives: The aim of this retrospective study was to investigate the lesions containing mature adipose tissues in surgical materials of the patients who underwent thyroidectomy operation owing to the diagnosis of nodular goiter.
Afşın Rahman Mürtezaoğlu +5 more
core +1 more source
Pelvic lipomatosis and renal transplantation: A case report
World Journal of Clinical Cases, 2020 BACKGROUND Pelvic lipomatosis is a rare disease of unknown etiology, characterized by the overgrowth of pelvic adipose tissue that causes compression of the urinary tract including the bladder and ureters, rectum and blood vessels.
Jie Zhao +3 more
semanticscholar +1 more source
KRAS Footprints in the Skin: Leveraging Targeted Therapy for Unresectable Intra‐Cerebral AVM
Pediatric Dermatology, EarlyView.ABSTRACT A 15‐year‐old female with a longstanding, unresectable intracerebral arteriovenous malformation (AVM) involving the bilateral thalami and basal ganglia presented with progressive neurologic decline. Given the inaccessibility of the intracranial lesion, a lipomatous scalp nodule overlying the AVM was biopsied for molecular testing and revealed ...
Donglin Zhang +5 more
wiley +1 more source
Idiopathic lumbosacral spinal epidural lipomatosis
PAMJ Clinical Medicine, 2020 A 45-year-old obese man, previously healthy, presented with a 7-month history of neurogenic claudication of both legs and bilateral sciatic radiculopathy without bowel or bladder disturbances.
Ali Akhaddar, Nabil Hammoune
doaj +1 more source
Do you know this syndrome? Type 2 benign symmetric lipomatosis (Launois-Bensaude) [PDF]
Anais Brasileiros de Dermatologia, 2016 A 57-year-old female showed bulky, loose tumors, which progressively spread to her arms, anterior chest, and back. She reported dysphagia and dyspnea after mild exertion. She denied alcohol consumption.
Ana Cláudia Cavalcante Esposito +3 more
doaj +1 more source
The Journal of Physiology, EarlyView.Abstract figure legend Mitochondria are highly dynamic organelles that continuously remodel their architecture through coordinated cycles of fusion and fission. This review examines the four key GTPases that orchestrate mitochondrial dynamics in mammals: MFN1, MFN2, OPA1, and DRP1.
Rémi Chaney +4 more
wiley +1 more source
Gastric lipomatosis treated by total gastrectomy: a case report
Surgical Case Reports, 2017 Background Gastric lipomatosis is characterized by multiple gastric lipomas or a diffuse gastric infiltration of the submucosal or subserosal layer by the adipose tissue; diffuse-type gastric lipomatosis is an extremely rare condition.
Shota Aoyama +5 more
doaj +1 more source