Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Related Concept Videos

Lysosomal Hydrolases01:22

Lysosomal Hydrolases

Lysosomes are the site for the degradation of macromolecules and biological polymers released during membrane trafficking events such as secretory, endocytic, autophagic, and phagocytic pathways. The membrane-enclosed area of the lysosome, called the lumen, contains hydrolytic enzymes active in an acidic environment. These acid hydrolases are functional at a pH between 4.5 and 5 and are involved in cellular processes such as cell signaling, energy metabolism, restoration of the plasma membrane,...
Pleiotropy01:33

Pleiotropy

Pleiotropy is the phenomenon in which a single gene impacts multiple, seemingly unrelated phenotypic traits. For example, defects in the SOX10 gene cause Waardenburg Syndrome Type 4, or WS4, which can cause defects in pigmentation, hearing impairments, and an absence of intestinal contractions necessary for elimination. This diversity of phenotypes results from the expression pattern of SOX10 in early embryonic and fetal development. SOX10 is found in neural crest cells that form melanocytes,...
Esophageal Achalasia01:27

Esophageal Achalasia

Esophageal achalasia is a chronic neurogenic disorder characterized by impaired relaxation of the lower esophageal sphincter (LES) and absent or ineffective peristalsis in the distal esophagus. This leads to a functional obstruction without a physical blockage, despite significant disruption of esophageal motility.EtiologyAchalasia is caused by degeneration of the myenteric (Auerbach's) plexus, specifically the loss of inhibitory ganglion cells that produce vasoactive intestinal peptide (VIP)...

You might also read

Related Articles

Articles linked to this work by shared authors, journal, and citation graph.

Sort by
Same author

A hierarchical cluster analysis for clinical profiling of tofacitinib treatment response in patients with rheumatoid arthritis.

Clinical rheumatology·2024
Same author

The APLAR Gout Registry: A multinational collaboration to better understand people with gout in the Asia-Pacific.

International journal of rheumatic diseases·2023
Same author

A summary of the Malaysian Clinical Practice Guidelines on the management of postmenopausal osteoporosis, 2022.

Osteoporosis and sarcopenia·2023
Same author

Prevalence and risk factors associated with psoriatic arthritis among patients with psoriasis.

International journal of rheumatic diseases·2023
Same author

Clinicohistological and immunopathological features of patients with cutaneous lupus erythematosus at tertiary dermatology centre in Malaysia.

Clinical and experimental dermatology·2022
Same author

2021 Asia-Pacific League of Associations for Rheumatology clinical practice guideline for treatment of gout.

International journal of rheumatic diseases·2021

Related Experiment Video

Updated: May 17, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
07:36

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Published on: May 1, 2015

Lemierre syndrome.

Ai Lee Lim1, Kin Choo Pua

  • 1Department of Otorhinolarngology, Hospital Pulau Pinang, Jalan Residensi, 10990 Penang. quenstanylim@hotmail.com

The Medical Journal of Malaysia
|October 23, 2012
PubMed
Summary

Lemierre syndrome, a rare but serious oropharyngeal infection, involves septic thrombophlebitis of the internal jugular vein. Prompt diagnosis and treatment are crucial for managing this potentially fatal condition.

Area of Science:

  • Infectious Diseases
  • Microbiology
  • Vascular Surgery

Background:

  • Lemierre syndrome, a rare condition, originates from acute bacterial oropharyngeal infections.
  • Historically known as "the forgotten fever," it was first described in 1900.
  • Fusobacterium necrophorum is the most common causative agent.

Observation:

  • The syndrome involves secondary septic thrombophlebitis of the internal jugular vein.
  • Embolization to the lungs and other organs can occur.
  • Diagnosis is often incidental, relying on unexpected culture results.

Findings:

  • Lemierre syndrome, though uncommon, remains a serious and potentially fatal illness.
  • It was particularly dangerous in the pre-antibiotic era.

More Related Videos

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
15:48

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies

Published on: July 29, 2007

Related Experiment Videos

Last Updated: May 17, 2026

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting
07:36

Isolation of Human Lymphatic Endothelial Cells by Multi-parameter Fluorescence-activated Cell Sorting

Published on: May 1, 2015

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies
15:48

ALS - Motor Neuron Disease: Mechanism and Development of New Therapies

Published on: July 29, 2007

  • Modern diagnosis often relies on identifying Fusobacterium necrophorum in blood cultures.
  • Implications:

    • Increased awareness and prompt diagnosis are vital for effective management.
    • Early recognition can prevent severe complications and mortality.
    • This case highlights the importance of considering Lemierre syndrome in oropharyngeal infections.