Literature DB >> 16339212

Emergencies in hereditary haemorrhagic telangiectasia.

M Gallitelli1, G Pasculli, T Fiore, A Carella, C Sabbà.   

Abstract

BACKGROUND: Hereditary haemorrhagic telangiectasia (HHT) is a systemic autosomal dominant vascular disease. Although the clinical picture is that of a chronic disabling disease, vascular malformations can suddenly lead to life-threatening conditions. AIM: To assess the frequency and type of emergency acute complications in HHT.
DESIGN: Retrospective case-note review.
METHODS: From August 2000 to December 2004, our specialized HHT centre saw 139 patients (74 males, 65 females, mean age 45.5 years, range 14-77) with a definite diagnosis of HHT. We reviewed their clinical files and recorded all visits for acute complications (massive nosebleeds, haematemesis, melaena, haematochezia, haemothorax, haemoptysis, TIA/ischaemic stroke, haemorrhagic stroke, brain abscess).
RESULTS: Fifty patients (35.9%) had at least one acute complication. There were a total of 93 visits potentially involving the emergency department. Most commonly, patients sought urgent medical attention for nosebleeds and gastrointestinal bleeding (63.4%), but there were also disorders of the brain, lung, heart and liver. DISCUSSION: Acute complications of HHT are not uncommon and can be severe and wide-ranging. Physicians should be aware of HHT and its major complications, as a prompt diagnosis is essential to direct patients to the most appropriate therapies, and to suggest screening for visceral involvement in their relatives.

Entities:  

Mesh:

Year:  2005        PMID: 16339212     DOI: 10.1093/qjmed/hci148

Source DB:  PubMed          Journal:  QJM        ISSN: 1460-2393


  4 in total

1.  Predictors of mortality in patients with hereditary hemorrhagic telangiectasia.

Authors:  K P Thompson; J Nelson; H Kim; L Pawlikowska; D A Marchuk; M T Lawton; Marie E Faughnan
Journal:  Orphanet J Rare Dis       Date:  2021-01-06       Impact factor: 4.123

2.  Definite hereditary hemorrhagic telangiectasia in a 60-year-old black Kenyan woman: a case report.

Authors:  Joan Chepkorir Kiyeng; Abraham Siika; Cornelius Koech; Gerald S Bloomfield
Journal:  J Med Case Rep       Date:  2016-05-25

3.  Spinal Arteriovenous Fistula, A Manifestation of Hereditary Hemorrhagic Telangiectasia: A Case Report.

Authors:  Jodi Spangler; Bjorn Watsjold; Jonathan S Ilgen
Journal:  Clin Pract Cases Emerg Med       Date:  2020-08

4.  A Rare Case of Upper Gastrointestinal Bleeding: Osler-Weber-Rendu Syndrome.

Authors:  Anna Jargielo; Anna Rycyk; Beata Kasztelan-Szczerbinska; Halina Cichoz-Lach
Journal:  Medicina (Kaunas)       Date:  2022-02-22       Impact factor: 2.430

  4 in total

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