Double chambered right ventricle with severe calcification of the tricuspid valve in an elderly woman: a case report

نویسندگان

  • Nozomu Tamai
  • Shigenori Ito
  • Kotaro Morimoto
  • Masahiko Inomata
  • Takayuki Yoshida
  • Shin Suzuki
  • Yoshimasa Murakami
  • Koichi Sato
چکیده

INTRODUCTION Double chambered right ventricle is a rare congenital cardiac anomaly in which the right ventricle is divided into two chambers by an anomalous muscle bundle. The diagnosis of this disorder is difficult in adults. Calcification of the tricuspid valve is extremely rare, and very few cases have been reported. Most cases of tricuspid valve calcification had a congenital disorder with high pressure in the right ventricle. CASE PRESENTATION We report a rare case of a 71-year-old Japanese woman who presented with chest discomfort, and was found to have a double chambered right ventricle with severe calcification of the tricuspid valve. This abnormality was found by echocardiography, and the diagnosis was confirmed by multislice cardiac computerized tomography, cardiac magnetic resonance imaging, and cardiac catheterization. Our patient rejected surgical repair, and medical therapy with carvedilol was effective to reduce her symptoms. CONCLUSION Calcification of the tricuspid valve is extremely rare, and considered to be due to high pressure in the right ventricle. To the best of our knowledge, there are no other reported cases of this combination of double chambered right ventricle and calcification of the tricuspid valve.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Calcific tricuspid incompetence in childhood.

Calcification of the tricuspid valve is rare. Previously reported cases have been associated with increased pressure in the right ventricle or a left-to-right shunt proximal to the tricuspid valve. Furthermore, the calcification has not been evident until the fifth decade of life or later. A case is reported here in which moderately severe tricuspid valve calcification was present ,at I0 years ...

متن کامل

Combined double chambered right ventricle, tricuspid valve dysplasia, ventricular septal defect, and subaortic stenosis in a dog

BACKGROUND Double chambered right ventricle (DCRV) is a congenital heart anomaly where the right ventricle is divided into two chambers. We describe, for the first time, an unusual combination of DCRV combined with some other congenital heart defects. CASE PRESENTATION A 1.2-year-old Golden Retriever was presented with lethargy, exercise intolerance and ascites. Physical examination revealed ...

متن کامل

Repair of very severe tricuspid regurgitation following detachment of the tricuspid valve

We report on the case of 5-year-old girl with severe tricuspid regurgitation following previous repair of double outlet right ventricle with subaortic ventricular septal defect, performed through trans-atrial approach using detachment of tricuspid valve leaflet. The severe tricuspid regurgitation was found to be due to dehiscence at the site of the previous detachment and was repaired using a p...

متن کامل

Double-chambered right ventricle.

A19-year-old woman with mild exercise intolerance was referred for follow-up examination of a known ventricular septal defect (VSD; Figure 1A). By continuous-wave Doppler, a gradient across the tricuspid valve of 60 mm Hg was recorded. The parasternal short-axis view revealed an anomalous muscle bundle with insertion at the interventricular septum and the right ventricular (RV) free wall (Figur...

متن کامل

A Case Report: A Newborn with Severe Ebstein's Anomaly in Hajar Hospital of Shahrekord

Background and Aims: Ebstein’s anomaly is an abnormal displacement downward of Tricuspid valve into the right ventricular, which is accompanied by myopathy of the right ventricular. It is found rarely with the prevalence of approximately 1:20000. Since the diagnosis of this disease in the appropriate position and time, the management of patients is important. This infant with Ebstein’s anomaly ...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:

دوره 5  شماره 

صفحات  -

تاریخ انتشار 2011