Congenital deficiency of the pericardium.

نویسندگان

  • J C Broadbent
  • J A Callahan
  • O W Kincaid
  • F H Ellis
چکیده

THE P A " ' PE"CAFm1"" MAY BE incompletely formed at birth, resulting in partial absence or deficiency of this membrane. As an isolated anomaly, the condition is rare. The subject was thoroughly reviewed by Ellis and assofiates' in 1959. Less than 120 validated c a m have been reported since that of Baillie' in 1793. Despite this rarity, the condition is of in-temt to the clinician and radiologist because it may simulate more serious cardiac pathology. It may be associated with defects of thoracic stmctures~ or with other forms of congenital heart disease? and it may be a cause of unusual thoracic symp toms. Prior to 1936, congenital absence of the pericardium had been recognized only at necromv. Since then. 29 c a m have been from three to 57 years and one female who was nine months old. The pericardial deficiency was associated with a ventricular septal defect in one patient and with patent ductus arteriosus in another. Two other patients had evidence of pulmonary di-ease, and three were studied b e c a w of suspected heart disease. One of these was found to have a large diaphragmatic hernia. In these five patients, no evidence of intrinsic cardiac disease was found. CASE REPORTS cAse I This patient was examined when he was 15 years old becaure of recurrent bouts of fever and hemoptysis during the preceding one and one-half yean. Bronchographic studies revealed bronchiectasb in the left upper lobe. A left up-w r lobectomv was carried out. At the time of. , diagnosed antemortem, 21 at o p operation in 1945, a large defect was noted in eration and eight by the demonstration the left side of the pericardium "through which a considerable partion of the heart could be of pneumopericardium after pneumotho-visualized." After the operation, recovery was A 57-year-old man underwent thoracotomy cases of absence of the pencar-for carcinoma of the left lung. The left side of dium are the pericardium was found to be a b w t. Thr the association of the anomaly with other right side was palpated and found to be intact. defects of thoracic structures, the eass of A left pneumonectomy was done, after which diagnosis by means of diagnostic pneumo-the heart could be rotated freely in the left side thorax, and the unique electrocardiogaph-of the chest. Atrial fibrillation appeared as a transient dysrhythmia three days after operation. ic in patients …

برای دانلود رایگان 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

CONGENITAL PARTIAL PERICARDIAL DEFECT WITH HERNIATION OF THE LEFT ATRIAL APPENDAGE

Congenital defects of the pericardium are considered rare. Until 1979 , the reported cases were only about 200.1 Total absence of the left pericardium is the most common defect2 and less common is a partial defect of the left pericardium. Other types, i.e. isolated right-sided defects, total pericardial absence and diaphragmatic pericardial defects are very rare.3 Before the last decade, t...

متن کامل

Congenital absence of the left pericardium and complete heart block. Report of a case.

FIGURE 1: Significant features include leftward displacement of the heart without tracheal deviation. In addition, three distinct convexities are noted along the left border of the heart. These are the aortic knob, pulmonary artery segment and the left ventricular contour. T HE RECOGNITION AND DEFINITIVE DIAGnosis of absent pericardium has gained impetus within recent years. Although well descr...

متن کامل

Congenital Partial Left Pericardial Defect with a Bronchogenic Cyst.

Congenital deficiency of the pericardium is a rare anomaly which is not mentioned in standard surgical textbooks. Rarer still is the association of this defect with a bronchogenic cyst. I have found only three references to it in the literature; one by Rusby and Sellors (1945), the second by Hamilton (1961), and the third one was a sequestrated lung cyst in a patient reported by Warner, Britt, ...

متن کامل

EXPERIENCE WITH 115 PATIENTS WITH CONGENITAL A DREN AL HYPERPLASIA AND EVALUATION OF GROWTH PATTERNS IN 24 PATIENTS WITH THE SALT-LOSING TYPE

In this study the data on 115 cases of congenital adrenal hyperplasia (CAH) who were followed in the Pediatric Endocrine Clinic at Nemazee Hospital, Shiraz will be reported. Among these cases 51 were male and 64 female. The most common type of CAH in these patients was the salt-losing type of 21 -hydroxylase deficiency (85 .2%). ll-hydroxylase deficiency was present in 13.04% of patients. ...

متن کامل

Indirect Molecular Diagnosis of Congenital Factor ΧІІІ Deficiency by Candidate Microsatellites and Single Nucleotide Polymorphisms

Background: Congenital factor XIII (FXIII) deficiency is one of the rarest bleeding disorders with a prevalence of one per 2 million in the general population. The disorder is accompanied by a high rate of life-threatening bleeding. Due to normal results of routine coagulation tests, diagnosis of the disorder is challenging, but molecular methods can be used for precise diagnosis. Direct mutati...

متن کامل

A Rare Case of Neonatal Birth with Congenital Bilateral Femoral Deficiency Undetected in Prenatal Ultrasound

Background:Prenatal ultrasound plays an important role in the early and accurate evaluation of the congenital skeletal and non-skeletal abnormalities of the fetus and is effective in predicting pregnancy outcomes. Congenital femoral deficiency (CFD) is a rare complicated and non-hereditary anomaly that includes the hypoplasia of a portion of the femoral bone with shortening the lower limb. Cas...

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

عنوان ژورنال:
  • Diseases of the chest

دوره 50 3  شماره 

صفحات  -

تاریخ انتشار 1966