Results 111 to 120 of about 20,160 (224)

Vasopressor‐Associated Limb Ischemia Resulting in Quadruple Amputation in Suspected Septic Shock

open access: yesClinical Case Reports, Volume 14, Issue 9, September 2026.
ABSTRACT Vasopressor‐associated limb ischemia (VALI) is a rare but devastating complication of vasopressor therapy in septic shock. This case shows catastrophic four‐limb amputation in a 26‐year‐old obese male with suspected septic shock. This case illustrates the complex interplay between prolonged high‐dose vasopressor therapy, morbid obesity, and ...
Muni Rubens   +8 more
wiley   +1 more source

Pediatric veno-arterial extracorporeal membrane oxygenation in fulminant hemophagocytic lymphohistiocytosis.

open access: yes, 2013
Pediatric veno-arterial extracorporeal membrane oxygenation in fulminant hemophagocytic ...
LUCIANI, GIOVANNI BATTISTA   +2 more
core   +1 more source

HEMOPHAGOCYTIC LYMPHOHISTIOCYTOSIS CASE PRESENTATION

open access: yes, 2019
Purpose: The purpose of this article is to discuss a case presentation of a rare form of acquired Hemophagocytic Lymphohistiocytosis (HLH) and review the standard of care in addition to current therapeutic options for the disease.
Delaney, Kristen, PA-C   +4 more
core   +1 more source

UNC13D is the predominant causative gene with recurrent splicing mutations in Korean patients with familial hemophagocytic lymphohistiocytosis

open access: yesHaematologica, 2010
Background Familial hemophagocytic lymphohistiocytosis is a fatal disease characterized by immune dysregulation from defective function of cytotoxic lymphocytes.
Hoi Soo Yoon   +19 more
doaj   +1 more source

Ruxolitinib Pharmacokinetics and Exposure–Toxicity Relationship in Hematologic Malignancies and Immune‐Mediated Diseases: A Prospective Observational Study

open access: yesClinical Pharmacology &Therapeutics, Volume 120, Issue 3, Page 753-761, September 2026.
Ruxolitinib pharmacokinetics (PK) has been characterized in clinical trials but remains poorly documented in real‐world practice. This project aimed to investigate ruxolitinib PK in routine clinical practice, identify factors driving its variability, and explore exposure–response relationships to assess the potential role of therapeutic drug monitoring.
Jérémie Tachet   +11 more
wiley   +1 more source

Fatal murine typhus with hemophagocytic lymphohistiocytosis in a child

open access: yes, 2020
Hemophagocytic lymphohistiocytosis is a rare complication in Rickettsia typhi infections. We report the case of a 2-year-old boy with sudden night-onset fever, pallor, neck adenopathy and erythematous macular rash on the thorax, thighs and buttocks ...
Juan J. Arias-León   +13 more
core   +1 more source

Pediatric Systemic Lupus Erythematosus Complicated by Acute EBV and CMV Co‐infection

open access: yesJournal of Clinical Laboratory Analysis, Volume 40, Issue 17, September 2026.
This case report describes a 10‐year‐old girl with new‐onset pediatric SLE who presented with malar rash, fever, and arthritis following sun exposure, alongside serological evidence of acute Epstein–Barr virus (EBV) and cytomegalovirus (CMV) co‐infection.
Anning Chen   +7 more
wiley   +1 more source

Primary Hemophagocytic Lymphohistiocytosis in an Infant

open access: yes, 2014
The paper considers the results of a clinical observation of an infant with hemophagocytic lymphohistiocytosis complicated with spontaneous splenic rupture.
T.A. Khalturyna   +7 more
core   +1 more source

Comprehensive Viral Detection and Profiling of Plasma Cell‐Free RNA in Patients With Suspected Hemophagocytic Lymphohistiocytosis

open access: yesJournal of Medical Virology, Volume 98, Issue 9, September 2026.
ABSTRACT Hemophagocytic lymphohistiocytosis (HLH) is a severe, rapidly progressive disease. While viral infection is considered a common etiology of pediatric HLH, specific causative viruses other than the Epstein‐Barr virus (EBV) have been rarely identified.
Yuto Fukuda   +12 more
wiley   +1 more source

Phenotypic and Genotypic Landscape of Sitosterolemia in China: Including a Rare Case With Nephronophthisis

open access: yesMolecular Genetics &Genomic Medicine, Volume 14, Issue 9, September 2026.
This study describes the first reported case of concurrent sitosterolemia (STSL) and nephronophthisis (NPHP). Additionally, we provide a systematic review of the clinical and genetic characteristics of Chinese STSL patients, representing the largest comprehensive cohort in China to date.
Dan Ding   +4 more
wiley   +1 more source

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