𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Unilateral megalencephaly associated with neonatal high output cardiac failure

✍ Scribed by Beverly C. Walters; Patricia E. Burrows; N. Musewe; S. H. Chuang; D. Armstrong


Publisher
Springer
Year
1990
Tongue
English
Weight
910 KB
Volume
6
Category
Article
ISSN
0256-7040

No coin nor oath required. For personal study only.

✦ Synopsis


High-flow cerebral arteriovenous fistulae are well known to present in the neonatal period with macrocephaly, cranial bruits and high-output cardiac failure. This report describes a newborn infant with such a clinical presentation, who had unilateral megalencephaly without macroscopic arteriovenous shunts. Ultrasound Doppler examination of the carotid and cerebral vessels showed diastolic flow, or a decreased pulsatility index, consistent with decreased intracranial vascular resistance. The ipsilateral cerebral arteries and veins were markedly enlarged at angiography and at post-mortem examination, but there was no arteriovenous malformation. The infant expired from high-output cardiac failure and hypoglycemia. It is postulated that the high-output cardiac failure was due to increased blood flow through the enlarged, dysplastic cerebral hemisphere.


πŸ“œ SIMILAR VOLUMES


Multiple myeloma associated with serum a
✍ Kuribayashi, Noriomi; Matsuzaki, Hiromitsu; Hata, Hiroyuki; Yoshida, Minoru; Son πŸ“‚ Article πŸ“… 1998 πŸ› John Wiley and Sons 🌐 English βš– 90 KB

We experienced a plasma cell leukemia (PCL) patient complicated with high output cardiac failure (HOCF), proved as his elevated cardiac index and pulmonary artery wedge pressure and decreased systemic vascular resistance index in a hemodynamic study. We found no possible causes of HOCF. Interestingl

High-output cardiac failure in a fetus w
✍ Fuat Akercan; Sevtap Oncul Seyfettinoglu; Burak Zeybek; Teksin Cirpan πŸ“‚ Article πŸ“… 2011 πŸ› John Wiley and Sons 🌐 English βš– 158 KB

## Abstract Placental chorioangioma is an angioma arising from chorionic tissue. Fetal thanatophoric dysplasia is a lethal skeletal dysplasia due to mutation of fibroblast growth factor receptor 3 gene. These two conditions are rare and their coexistence in a given fetus is even rarer. We present a

Intrauterine assessment of high-output c
✍ R. Achiron; R. Rabinovitz; Y. Aboulafia; Y. Diamant; J. Glaser πŸ“‚ Article πŸ“… 1992 πŸ› John Wiley and Sons 🌐 English βš– 688 KB

Twin-twin transfusion syndrome (TTTS) is a severe in utero complication of monozygotic twin pregnancies. It occurs as a result of blood transfer through anastomotic vessel in the placenta.' Both acute and chronic forms of TTTS have been clinically described. In the acute form, a significant amount o