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Tongue telangiectasia

MedGen UID:
871382
Concept ID:
C4025878
Anatomical Abnormality
Synonyms: Angioectasias of the tongue; Lingual angioectasias; Lingual telangiectasia; Spider veins of the tongue
 
HPO: HP:0000227

Definition

Telangiectasia (that is, the presence of small dilated superficial blood vessels) of the tongue. [from HPO]

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVTongue telangiectasia

Conditions with this feature

Telangiectasia, hereditary hemorrhagic, type 2
MedGen UID:
324960
Concept ID:
C1838163
Disease or Syndrome
Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct connections between arteries and veins. The most common clinical manifestation is spontaneous and recurrent nosebleeds (epistaxis) beginning on average at age 12 years. Telangiectases (small AVMs) are characteristically found on the lips, tongue, buccal and gastrointestinal (GI) mucosa, face, and fingers. The appearance of telangiectases is generally later than epistaxis but may be during childhood. Large AVMs occur most often in the lungs, liver, or brain; complications from bleeding or shunting may be sudden and catastrophic. A minority of individuals with HHT have GI bleeding, which is rarely seen before age 50 years.
Hereditary hemorrhagic telangiectasia type 4
MedGen UID:
341824
Concept ID:
C1857688
Disease or Syndrome
Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct connections between arteries and veins. The most common clinical manifestation is spontaneous and recurrent nosebleeds (epistaxis) beginning on average at age 12 years. Telangiectases (small AVMs) are characteristically found on the lips, tongue, buccal and gastrointestinal (GI) mucosa, face, and fingers. The appearance of telangiectases is generally later than epistaxis but may be during childhood. Large AVMs occur most often in the lungs, liver, or brain; complications from bleeding or shunting may be sudden and catastrophic. A minority of individuals with HHT have GI bleeding, which is rarely seen before age 50 years.
Telangiectasia, hereditary hemorrhagic, type 1
MedGen UID:
1643786
Concept ID:
C4551861
Disease or Syndrome
Hereditary hemorrhagic telangiectasia (HHT) is characterized by the presence of multiple arteriovenous malformations (AVMs) that lack intervening capillaries and result in direct connections between arteries and veins. The most common clinical manifestation is spontaneous and recurrent nosebleeds (epistaxis) beginning on average at age 12 years. Telangiectases (small AVMs) are characteristically found on the lips, tongue, buccal and gastrointestinal (GI) mucosa, face, and fingers. The appearance of telangiectases is generally later than epistaxis but may be during childhood. Large AVMs occur most often in the lungs, liver, or brain; complications from bleeding or shunting may be sudden and catastrophic. A minority of individuals with HHT have GI bleeding, which is rarely seen before age 50 years.

Professional guidelines

PubMed

Li S, Wang SJ, Zhao YQ
Medicine (Baltimore) 2018 Aug;97(31):e11687. doi: 10.1097/MD.0000000000011687. PMID: 30075565Free PMC Article
Papaspyrou G, Schick B, Al Kadah B
ORL J Otorhinolaryngol Relat Spec 2016;78(5):245-251. Epub 2016 Aug 4 doi: 10.1159/000447949. PMID: 27486666
Peng HL, Yi YF, Zhou SK, Xie SS, Zhang GS
Chin Med J (Engl) 2015 Nov 20;128(22):3050-4. doi: 10.4103/0366-6999.169068. PMID: 26608985Free PMC Article

Recent clinical studies

Diagnosis

Bowers EMR, Lee S
BMJ Case Rep 2020 Nov 2;13(11) doi: 10.1136/bcr-2020-238485. PMID: 33139375Free PMC Article

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