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Did angiodysplasia associated with heyde's syndrome disappear spontaneously?: a case report.
Li, Rui; Ji, Shuliang; Shi, Jiaxi; Qing, Lijin; Wu, Wei; Zhang, Jiechun.
Afiliación
  • Li R; Department of Cardiovascular Medicine, General Hospital of Southern Theater Command of PLA, Guangzhou, China.
  • Ji S; Department of Traditional Chinese Medicine, Shantou University Medical College, Shantou, China.
  • Shi J; Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Qing L; Department of Cardiovascular Medicine, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Wu W; Department of Cardiovascular Medicine, The First Affiliated Hospital of Guangzhou University of Chinese Medicine, Guangzhou, China.
  • Zhang J; The affiliated TCM Hospital of Guangzhou Medical University, Guangzhou, China. 2022621573@gzhmu.edu.cn.
J Cardiothorac Surg ; 18(1): 225, 2023 Jul 10.
Article en En | MEDLINE | ID: mdl-37430321
ABSTRACT

BACKGROUND:

Heyde's syndrome can be easily overlooked or misjudged in clinical practice because it shares common clinical manifestations with multiple diseases as well as limited accuracy of several corresponding examinations for diagnosing Heyde's triad. Moreover, aortic valve replacement is often delayed in these patients due to the contradiction between anticoagulation and hemostasis. Herein, we present a rare case of atypical Heyde's syndrome. The patient's severe intermittent gastrointestinal bleeding was not completely cured even through a local enterectomy. In the absence of direct evidence of acquired von Willebrand syndrome (AVWS) or angiodysplasia, her long-standing gastrointestinal bleeding was finally stopped after receiving transcatheter aortic valve implantation (TAVI). CASE PRESENTATION A 64-year-old female suffered from refractory gastrointestinal bleeding and exertional dyspnoea. A local enterectomy was performed owing to persistent hemorrhage and repeated transfusions; subsequently, histological examination revealed angiodysplasia. Heyde's syndrome was not suspected until 3 years later, at which time the patient started bleeding again and was also found to have severe aortic valve stenosis upon echocardiography. TAVI was consequently performed when the patient was in a relatively stable condition even though the predisposition to bleed, but there was no evidence of angiodysplasia and AVWS during angiography at that time. The patient's above symptoms were significantly relieved after TAVI and followed up for 2 years without any significant ischemic or bleeding events.

CONCLUSIONS:

The visible characteristics of angiodysplasia or a shortage of HMWM-vWFs should not be indispensable for the clinical diagnosis of Heyde's syndrome. Enterectomy could be a bridging therapy for aortic valve replacement in patients with severe hemorrhage, and TAVI may be beneficial for moderate to high surgical-risk patients even if they have a potential risk of bleeding.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Angiodisplasia / Enfermedades del Colon Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: J Cardiothorac Surg Año: 2023 Tipo del documento: Article País de afiliación: China

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Angiodisplasia / Enfermedades del Colon Tipo de estudio: Diagnostic_studies / Etiology_studies / Risk_factors_studies Límite: Female / Humans / Middle aged Idioma: En Revista: J Cardiothorac Surg Año: 2023 Tipo del documento: Article País de afiliación: China