scholarly journals “Hæmorrhagic shock”; its cause, and influence on pregnancy

1922 ◽  
Vol 3 (2) ◽  
pp. 625-631
Author(s):  
E. Hastings Tweedy
Keyword(s):  
1979 ◽  
Vol 39 (7) ◽  
pp. 653-658 ◽  
Author(s):  
Morten Kveim ◽  
Ragnar Nesbakken
Keyword(s):  

Resuscitation ◽  
2013 ◽  
Vol 84 (3) ◽  
pp. 397-398
Author(s):  
Hsi-Ning Chu ◽  
Pei-Shan Tsai ◽  
Tao-Yeuan Wang ◽  
Chun-Jen Huang

1993 ◽  
Vol 10 (3) ◽  
pp. 135-137 ◽  
Author(s):  
P Diprose ◽  
R A Sleet
Keyword(s):  

2020 ◽  
Vol 13 (8) ◽  
pp. e235549
Author(s):  
Skand Shekhar ◽  
Julie Chen ◽  
Kaniksha Desai

A middle-aged woman with end-stage renal disease (ESRD) due to obstructive nephropathy presented to the hospital for an episode of unresponsiveness and hypoglycaemia. Initially, she was diagnosed with hypoglycaemia associated with ESRD and was discharged. However, she returned to the hospital after experiencing tonic–clonic seizures and recurrent hypoglycaemia. Her hypoglycaemia workup revealed an elevated insulin-like growth factor 2 (IGF2) to IGF1 ratio consistent with paraneoplastic IGF2 secretion. Subsequently, a CT abdomen revealed a retroperitoneal mass, found to be a retroperitoneal sarcoma. Her hypoglycaemia was treated with glucocorticoids and growth hormone. Surgical debulking of her tumour was attempted, but she expired due to postoperative haemorrhagic shock. Doege-Potter syndrome is a rare cause of hypoglycaemia which should be suspected in any new-onset, worsening, inexplicable or refractory hypoglycaemia, particularly in non-diabetic ESRD. Here we present a report of retroperitoneal sarcoma presenting with hypoglycaemia in a patient with ESRD without diabetes.


2020 ◽  
Vol 13 (2) ◽  
pp. e231995
Author(s):  
Brittany Sanford ◽  
Catherine Hoeppner ◽  
Tammy Ju ◽  
Brian K Theisen ◽  
Anna BuAbbud ◽  
...  

Management of a ruptured hepatocellular adenoma during pregnancy is a rare and potentially life-threatening entity. Few case reports have described management of the pregnant patient who presents in haemorrhagic shock secondary to a ruptured liver adenoma. A 30-year-old primigravid woman at 31 weeks pregnant presented with abdominal pain and fetal bradycardia. After stat caesarean delivery of the infant, she had continued hemoperitoneum and was in shock secondary to an undiagnosed ruptured liver mass. General surgery was consulted intraoperatively and performed an exploratory laparotomy, packing and temporary closure. She was subsequently taken to interventional radiology (IR) for angioembolisation of the left hepatic artery. After stabilisation, she underwent formal abdominal closure. Management of a ruptured hepatocellular adenoma in pregnancy requires urgent multidisciplinary care including obstetrics gynaecology, general surgery and IR.


2012 ◽  
Vol 5 (2) ◽  
pp. 143
Author(s):  
Nicolas Morel ◽  
Laurent Merson ◽  
Jean-Christophe Bernard ◽  
Philippe Dabadie ◽  
Cyrille Chabarttier ◽  
...  

2011 ◽  
Vol 107 (5) ◽  
pp. 719-725 ◽  
Author(s):  
T. Kurita ◽  
M. Uraoka ◽  
K. Morita ◽  
M. Suzuki ◽  
Y. Morishima ◽  
...  

2008 ◽  
Vol 25 (1) ◽  
pp. 81-83 ◽  
Author(s):  
A. Menzebach ◽  
C. Mutz ◽  
T. W. L. Scheeren
Keyword(s):  

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