Co-Occurrence of Natal Teeth With Rapidly Involuting Congenital Hemangioma: A Case Report

نویسندگان
چکیده

برای دانلود باید عضویت طلایی داشته باشید

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

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Rapidly involuting congenital hemangioma*

Rapidly involuting congenital hemangioma is a rare vascular tumor that generally has a good prognosis. The authors describe a case of a newborn girl with a left cervical vascular lesion. Image exams were performed, and the lesion slowly decreased, leaving redundant skin. Considering all of the findings, a final diagnosis of a rapidly involuting congenital hemangiomas was suspected.

متن کامل

Rapidly involuting congenital hemangioma.

Volume 95 No. 5 May 2012 a newborn Male, delivered by Caesarean section after induction at 41 weeks of gestation for failure to progress, was admitted to the Women and Infants’ Hospital (WIH) Neonatal Intensive Care Unit (NICU) with a large vascular mass on his left knee (Figure 1). Routine prenatal US had been normal and the pregnancy had been uneventful. Physical examination at delivery was o...

متن کامل

Rapidly Involuting Congenital Hemangioma of the Hand

Figure 1. Right hand with rapidly involuting congenital hemangioma.

متن کامل

Multiple Successful Angioembolizations for Refractory Cardiac Failure in a Preterm with Rapidly Involuting Congenital Hemangioma

Rapidly involuting congenital hemangiomas (RICH) are the commonest variety of congenital hemangioma, often diagnosed antenatally as high-flow arteriovenous shunts causing hemodynamic compromise to the fetus. The postnatal management of such patients is often challenging. We present the case of an infant boy who was delivered prematurely at 29 weeks of gestation due to fetal compromise by a RICH...

متن کامل

A rare atypical rapidly involuting congenital hemangioma combined with vascular malformation in the upper limb

BACKGROUND Rapidly involuting congenital hemangioma is a congenital soft tissue tumor, which is difficult to excise completely and rather prone to recur. This atypical tumor combined with capillary-lymphatic-venous malformation was not reported in the literature. CASE PRESENTATION We report an atypical case of a 16-year-old teenager who was born with a mass in his right upper limb. Since ther...

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

ژورنال

عنوان ژورنال: Journal of Medical Cases

سال: 2016

ISSN: 1923-4155,1923-4163

DOI: 10.14740/jmc2433w