Giant congenital diverticula and neonatal rupture of colon: A case associated with true congenital partial hypertrophy of the crossed type.

نویسنده

  • J E Morison
چکیده

Clinical history. The patient died on the twelfth day of life, having been delivered by a Caesarian operation for disproportion. He was difficult to resuscitate at birth and the abdomen always appeared distended. This distension varied somewhat, but there were no other unusual symptoms until he suddenly collapsed and died in two hours. Post-mortem examination. The body was that of a well-nourished male infant. The left side of the cranium and face, especially the mandible and ear, was larger than the right. This asymmetry was less marked posteriorly. No certain difference could be detected in the arms, thorax or abdomen, but the left leg was 2 cm. shorter than the right and this was largely accounted for by the shortening of the femur. The thickness of the thigh was proportionately altered, but asymmetry of the feet was not detected. On opening the cranium the left anterior and middle fossae of the skull were obviously larger than the right, but the disporportion between the posterior fossae was less certain. The cerebral convolutions were normal, but the cerebrum and even the cerebellum and pons shared in the asymmetry of the skull. No asymmetry of the thoracic or abdominal organs was demonstrable. Except for the pelvic colon the contents of the thorax and abdomen were normal. The colon had a long free mesentery and lying in it, and slightly behind the bowel and almost 7 cm. from the anus, there was a cystic cavity 4 cm. from side to side, 3 5 cm. from above downwards and 2 cm. from front to back (fig. 1). This communicated with the lumen of the bowel by an orifice 1-2 cm. by 0 5 cm. in diameter. Its walls were 2 to 3 mm. thick, but showed no condensation of muscle into bands. Beginning 4-5 cm. above this opening and extending for 3 0 cm. the mesenteric wall of the bowel was expanded into a similar cavity with thick walls. Both diverticula received their blood supply from the arcade of the inferior mesenteric artery. The superior cavity extended 1-0 cm. above and 1 5 cm. below its wide entrance, and when it was dilated the part below the opening was capable of compressing the adjacent bowel and producing obstruction. Immediately opposite this upper aneurysmal like

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

Partial Ectopia Cordis: A Case Report

Background: One-third of all major congenital anomalies are Congenital heart disease (CHD) and Reported CHD prevalence increased over time and in Asian countries is more than western countries. Ectopia cordis (EC) is a rare congenital anomaly with an estimated incidence of 1:100 000 live births in developed countries. EC is characterized by abnormal heart placement outside the thorax, mostly on...

متن کامل

Congenital Diverticular Disease of the Entire Colon

Congenital or true colonic diverticulosis is a rare condition typified by the preservation of the colonic wall architecture within the diverticular outpouching. Cases of multiple jejunal diverticula have been reported as well as cases of solitary giant diverticula of the colon. There have been no reports in the literature of pancolonic congenital diverticulosis.

متن کامل

Pacman Heart as a Congenital Cardiac Defect Associated with Flail Mitral Valve and a Partial form of Shone\'s Complex; A Case Report

Partial muscular inter-ventricular septal defect (VSD) or Pacman heart is a rare congenital or occasionally acquired anomaly. Concurrent Pacman heart and Shone's complex are extremely rare and have never been reported until now. We described a 37-year-old male patient with congenital Pacman heart, flail mitral valve (FMV), and a history of multiple congenital anomalies, including subvalvular ao...

متن کامل

Giant Congenital Diverticula and Neonatal Rupture of Colon: a Case Associated with True Congenital Partial Hypertrophy of the Crossed Type

Clinical history. The patient died on the twelfth day of life, having been delivered by a Caesarian operation for disproportion. He was difficult to resuscitate at birth and the abdomen always appeared distended. This distension varied somewhat, but there were no other unusual symptoms until he suddenly collapsed and died in two hours. Post-mortem examination. The body was that of a well-nouris...

متن کامل

Complete Congenital Heart Block in a Neonatal Lupus Erythematosus Associated with Pulmonary Involvement without Pacemaker Implantation: A Case Report

Background: Neonatal lupus erythematosus is an uncommon disease. Congenital complete heart block (CCHB) usually happens in neonates with maternal systemic lupus erythematosus. The most prevalent presentation of CCHBis bradycardiathatcanbediagnosed through an electrocardiogram. Case report: Here in, we present the case of a full-term male neonate with gestational age of 37 weeks and birth weigh...

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:
  • Archives of disease in childhood

دوره 19 99  شماره 

صفحات  -

تاریخ انتشار 1944