Open AccessA case of hereditary hemorrhagic telangiectasia and literature review
Author(s) -
Han Yu,
Ding Bingjie,
Li Mengjuan,
Song Xuewen,
Liu Liu,
Zhou Hu
Publication year - 2022
Publication title -
journal of clinical laboratory analysis
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.536
H-Index - 50
eISSN - 1098-2825
pISSN - 0887-8013
DOI - 10.1002/jcla.24571
Subject(s) - telangiectasia , medicine , anemia , iron deficiency anemia , surgery , outpatient clinic , iron deficiency , pediatrics , dermatology
Background To discuss the clinical features of a patient with hereditary hemorrhagic telangiectasia (HHT). Methods The clinical data of one patient with HHT are retrospectively analysed. In addition, we review the relevant literature. Results A 32‐year‐old male patient was admitted to the hematology outpatient department of our hospital and presented with intermittent epistaxis for 24 years. In recent years, he was diagnosed with iron deficiency anemia. The nasal endoscopic examination showed telangiectasia at the front of the right‐middle turbinate and the left nasal cavity. He had ENG genetic mutation positivity. Conclusions Patients with HHT may suffer from many complications, including bleeding, anemia, iron deficiency, and high‐output heart failure. These patients may have telangiectasias and arteriovenous malformations in various organs.