A Rare Case of Fatal Thyroid Storm (TS) Resulting in DIC and Multiorgan Failure

CHEST Journal ◽  
2014 ◽  
Vol 146 (4) ◽  
pp. 302A
Author(s):  
Amareshwar Podugu ◽  
Khulood Rizvi ◽  
Chandra Dasari ◽  
Asha Chakka ◽  
Nihad Boutros
2002 ◽  
Vol 81 (8) ◽  
pp. 570-574 ◽  
Author(s):  
Neil M. Vora ◽  
Fred Fedok ◽  
Brendan C. Stack

Thyroid storm is a potentially life-threatening endocrinologic emergency characterized by an exacerbation of a hyperthyroid state. Several inciting factors can instigate the conversion of thyrotoxicosis to thyroid storm; trauma is one such trigger, but it is rare. Patients with thyroid storm can manifest fever, nervous system disorders, gastrointestinal or hepatic dysfunction (e.g., nausea, vomiting, diarrhea, and/or jaundice), and arrhythmia and other cardiovascular abnormalities. Treatment of thyroid storm is multimodal and is best managed by the endocrinologist and medical intensivist. Initial medical and supportive therapies are directed at stabilizing the patient, correcting the hyperthyroid state, managing the systemic decompensation, and treating the underlying cause. Once this has been achieved, definitive treatment in the form of radioactive ablation or surgery should be undertaken. We describe a case of thyroid storm in a young man that was precipitated by a motor vehicle accident.


Thyroid ◽  
2010 ◽  
Vol 20 (3) ◽  
pp. 333-336 ◽  
Author(s):  
Hui Wen Chong ◽  
Kay Choong See ◽  
Jason Phua

2016 ◽  
Vol 44 (12) ◽  
pp. 497-497
Author(s):  
Junad Chowdhury ◽  
Vishad Sheth ◽  
Asif Abdul Hameed ◽  
Ana Maheshwari ◽  
Komal Patel ◽  
...  
Keyword(s):  

Author(s):  
Valeria Di Stefano ◽  
Margherita Migone De Amicis ◽  
Cecilia Bonino ◽  
Natalia Scaramellini ◽  
Yvan Torrente ◽  
...  

Objective: We describe a rare case of group G streptococcus (GGS) sepsis complicated by bacterial toxin myopathy. Case: A 65-year-old man, with a history of infection of his shoulder prosthesis, presented with multiorgan failure and notable myalgia likely caused by toxins. The patient was treated successfully with antibiotics and prosthesis removal. Conclusion: This case suggests infection by GGS should be considered in a patient presenting with myalgia associated with sepsis.


2021 ◽  
Vol 5 (Supplement_1) ◽  
pp. A923-A924
Author(s):  
Zaina Abdelhalim Alamer ◽  
Mohammed Alkhatib ◽  
Emad Naem ◽  
Noor Nabeel M Suleiman ◽  
Marwa Gomaa Mokhtar ◽  
...  

Abstract Background: Thyroid storm is a rare complication of hyperthyroidism. It can lead to life-threatening complications such as Arrhythmias, multiorgan failure and disseminated intravascular coagulation (DIC) (1). In pregnant patients can cause spontaneous abortions, fetal demise (2). Aggressive treatment under critical care settings is needed. Clinical Case: We report a case of 24-year-old Indian female twelve weeks pregnant; background of Graves’ disease for five years, was on carbimazole but she discontinued since she became pregnant. Presented to Hamad general hospital with nausea, vomiting and altered mental status for one day. She was afebrile, normotensive, tachypneic, tachycardiac with heart rate of 150bpm, and confused. Investigations showed supraventricular tachycardia aborted by adenosine and amiodarone, TSH was < 0.01mIU/l(0.3-4.2) and FT4> 100 pmol/L(11.6-21.9),normal baseline liver function and complete blood counts. In the emergency department, she was managed for thyroid storm with hydrocortisone, propranolol, propylthiouracil (PTU), iodine solution and cholestyramine. Then suddenly she deteriorated requiring intubation and vasopressor support under care of Medical Intensive Care Unit (MICU) progressed to multiorgan failure; acute liver injury, acute kidney injury and DIC. So, PTU was stopped and started on plasma exchange followed by total thyroidectomy and tracheostomy. US pelvis showed nonviable fetus, so dilation and curettage were done by obstetric team. Afterwards, she markedly improved except her conscious level and kidney function which required Hemodialysis. MRI brain showed small subdural hematoma treated conservatively and Wernicke encephalopathy treated with thiamine with substantial response and spontaneously breathing. Post thyroidectomy she required calcium supplementation and levothyroxine, liver function and coagulation parameters back to baseline. Conclusion: Thyroid storm in pregnancy is a medical emergency with high mortality rate, it needs high index of suspicion and early aggressive management by a multidisciplinary team. Plasmapheresis may be considered for challenging cases as a bridge for definitive therapy. Thyroidectomy may be the only option in selected cases like our case. References: 1. Karger S, Führer D. Thyreotoxische Krise--ein Update [Thyroid storm--thyrotoxic crisis: an update]. Dtsch Med Wochenschr. 2008 Mar;133(10):479-84. German. doi: 10.1055/s-2008-1046737. PMID: 18302101. 2. Ma Y, Li H, Liu J, Lin X, Liu H. Impending thyroid storm in a pregnant woman with undiagnosed hyperthyroidism: A case report and literature review. Medicine (Baltimore). 2018;97(3):e9606. doi:10.1097/MD.0000000000009606


Author(s):  
Sanjay Singh ◽  
Manash Biswas ◽  
Tony Jose ◽  
Madhusudan Dey ◽  
Monica Saraswat

2019 ◽  
Author(s):  
Win Khine ◽  
James MacFarlane ◽  
Martin Lee ◽  
Katy Rice ◽  
Myint Khin Swe

Author(s):  
Valeria Di Stefano ◽  
Margherita Migone De Amicis ◽  
Cecilia Bonino ◽  
Natalia Scaramellini ◽  
Yvan Torrente ◽  
...  

Objective: We describe a rare case of group G streptococcus (GGS) sepsis complicated by bacterial toxin myopathy. Case: A 65-year-old man, with a history of infection of his shoulder prosthesis, presented with multiorgan failure and notable myalgia likely caused by toxins. The patient was treated successfully with antibiotics and prosthesis removal. Conclusion: This case suggests infection by GGS should be considered in a patient presenting with myalgia associated with sepsis.


2019 ◽  
Vol 12 (5) ◽  
pp. e227747 ◽  
Author(s):  
Ivor Popovich ◽  
Vikrant Singh ◽  
Bevan Vickery

Fat embolism syndrome (FES) is a serious complication of trauma that can result in multiorgan failure, including the acute respiratory distress syndrome. Occasionally, the severity of respiratory failure associated with FES warrants support with venovenous extracorporeal membrane oxygenation (VV-ECMO), a therapy with widespread use but inconclusive evidence. Early definitive fracture fixation is the mainstay of preventing further fat embolism and ongoing organ dysfunction, but poses significant risks to the maintenance of the extracorporeal circuit. We describe a rare case of a patient who required VV-ECMO for respiratory support prior to fracture fixation. The risks of intraoperative fat embolisation causing sudden circuit failure were managed by having a spare circuit available outside the operating room with readiness for an emergency circuit change. Postoperative fat deposition in the oxygenator was managed by a circuit change. Our case is the first to describe preoperative initiation of VV-ECMO for FES and highlights why this therapy should not delay definitive fracture fixation and how it can be safely managed in this setting.


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