raremaprare-disease reference indexOrphadata 2026-06-23 · HPO 2026-09-01
ORPHA:137839

Lemierre syndrome

Synonyms: Lemierre postanginal sepsis · Postanginal sepsis secondary to orophyngeal infection · Septic phlebitis of the internal jugular vein

Type
Disease
Group
Disorder
Age of onset
Adolescent
Status
active

Lemierre syndrome is a rare, potentially lethal, oropharyngeal infectious disease occurring in immunocompetent adolescents and young adults that is mainly due to <i>Fusobacterium necrophorum</i> and that is characterized by septic thrombophlebitis of the internal jugular vein that leads to septic, usually pulmonary, embolism, associated with ENT (ear, nose, and throat) infection that manifests with fever, neck pain, and tonsillopharyngitis.

1

Names in Orphadata languages

12 of 12 languages
LangNameSynonyms
enLemierre syndromeLemierre postanginal sepsis · Postanginal sepsis secondary to orophyngeal infection · Septic phlebitis of the internal jugular vein
frSyndrome de LemierreSepsis post-angine de Lemierre · Sepsis post-angine secondaire à une infection oropharyngée · Thrombophlébite septique de la veine jugulaire interne
deLemierre-SyndromPostangina-Sepsis Lemierre · Postanginale Sepsis nach oropharyngealer Infektion · Septische Phlebitis der internen Jugularvene
esSíndrome de LemierreFlebitis séptica de la vena yugular interna · Sepsis postangina secundaria a infección orofaríngea · Sepsis postanginal de Lemierre · Sepsis postanginal secundaria a una infección orofaríngea
itSindrome di LemierreFlebite settica della vena giugulare interna · Sepsi post-angina di Lemierre · Sepsi post-angina secondaria a infezioni orofaringee
nlLemierresyndroomPostanginale sepsis secundair aan orofaryngeale infectie · Postanginale sepsis van Lemierre · Septische flebitis van de inwendige halsader
ptSíndrome de Lemierre
plZespół Lemierre'aPoanginowa posocznica Lemierre'a · Septyczne zapalenie żyły szyjnej wewnętrznej · Wtórna posocznica poanginowa po infekcji gardła
csLemierrův syndromLemierrova postanginózní sepse · Sekundární postanginózní sepse po orofaryngeální infekci · Septická flebitida vnitřní krční žíly
ukСиндром ЛемєраПостангінальний сепсис Лемєра · Постангінальний сепсис, спричинений інфекцією ротоглотки · Септичний флебіт внутрішньої яремної вени
zhLemierre综合征口咽部感染所致咽峡后脓毒血症
trLemierre sendromuLemierre postanginal sepsis · İç juguler venin septik flebiti · Orofingeal enfeksiyona sekonder postanginal sepsis

Definition in:

2

Cross-references

qualifier = Orphanet mapping relation
SourceCodeQualifierICD relationValidation
ICD-10I80.8NTBTattributedvalidated
ICD-111C4YNTBTattributedvalidated
MONDO0015306Evalidated
MeSHD057831Evalidated
UMLSC0343525Evalidated
GARD6882Evalidated
MedDRA10065552Evalidated

E exact · NTBT this ORPHAcode is narrower than the target · BTNT broader than the target · ND not decided.

3

Classification

Preferential parent (Orphanet linearisation):

Parents in the classifications (1):

No children.

4

Genes

0 direct

Orphanet records no gene directly on this code.

5

Prevalence and incidence

3 records
TypeClassValueAreaQualificationValidationSource
Annual incidence1-5 / 10 00010 / 100 000EuropeValue and classNot yet validated20181152[PMID]
Annual incidence1-5 / 10 00036 / 100 000DenmarkValue and classValidated22633566[PMID]
Point prevalenceUnknown—WorldwideClass onlyNot yet validatedORPHANET

Value is Orphadata's ValMoy: the mean estimate per 100 000 for prevalence and incidence, the number of cases or families for case reports.

6

HPO phenotypes

Orphanet has no HPO annotation for this code in this release.

7

Sources for this card