scholarly journals Disseminated Intravascular Coagulation after Myomectomy: A Case Report and Review of Literature

2013 ◽  
Vol 4 (1) ◽  
pp. 31-33 ◽  
Author(s):  
Mousumi Acharya ◽  
Vandana Kamath ◽  
TK Aleyamma

ABSTRACT Hematological complications can complicate the postoperative period following myomectomy. Clinicians should keep such rarer possibilities in mind which will help them identify the complications correctly and manage appropriately. We managed a case of disseminated intravascular coagulation following myomectomy which was promptly diagnosed and managed. How to cite this article Kamath MS, Acharya M, Kamath V, Aleyamma TK. Disseminated Intravascular Coagulation after Myomectomy: A Case Report and Review of Literature. Int J Infertility Fetal Med 2013;4(1):31-33.

2019 ◽  
Vol 12 (8) ◽  
pp. e230160
Author(s):  
Jyotsna M Kirtane ◽  
Snehal A Bhange ◽  
Fazal Nabi ◽  
Varshil Shah

This is a case report of a neonate who was antenatally diagnosed with jejunal atresia which turned out to be duodenal atresia with apple peel syndrome. A previous sibling, who also had apple peel but with jejunal atresia, succumbed to sepsis after surgery. The first sibling had jejunal stenosis and had died of sepsis following surgery. Combination of duodenal atresia with apple peel is extremely rare. This coupled with a familial condition is rarer still. This case was challenging due to the short length of the gut and prolonged need for total parenteral nutrition and sepsis in postoperative period.


2018 ◽  
Vol 32 (3) ◽  
pp. 458-461
Author(s):  
G. Venkateswara Prasanna ◽  
Sathish Kumar Vandanapu ◽  
Hima Bindu

Abstract Bilateral extradural haematomas [EDH] are rare and it is an uncommon consequense of cranio cerebral trauma. The mortality is higher than unilateral extradural haematoma and management of extradural haematomas requires careful planning, judicial surgical exposure and most important is timing of evacuation of extradural haematomas. Emergency evacuation of bilateral extradural haematomas were performed in this case with uneventful postoperative period. The pathophysiology and surgical nuances of this rare entity been discussed.


2021 ◽  
Vol 9 (1) ◽  
pp. 292-296
Author(s):  
Orgeness J Mbwambo ◽  
Alex Mremi ◽  
Mohamed Mbarouk ◽  
Jasper Mbwambo ◽  
Frank Bright ◽  
...  

Urethral duplication is a rare congenital anomaly affecting mainly males. Here, we report a case of urethral duplication in a 19 years old male presented as a scrotal sinus discharging pus for 1 year. Surgical removal of accessory urethra was done and postoperative period was uneventful.


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