scholarly journals Pneumomediastinum, Pneumopericardium, and Epidural Pneumatosis following Adenotonsillectomy: A Very Rare Complication

2018 ◽  
Vol 2018 ◽  
pp. 1-4 ◽  
Author(s):  
Feride Fatma Görgülü ◽  
Ayşe Selcan Koç ◽  
Orhan Görgülü
Keyword(s):  
Carotid Artery ◽  
Subcutaneous Emphysema ◽  
Early Recognition ◽  
Rare Complication ◽  
Rare Condition ◽  
Male Child ◽  
Radiological Findings ◽  
Unique Case ◽  
Unusual Condition ◽  
Taste Disorders

Adenotonsillectomy is a common surgical otolaryngology procedure that is associated with several complications, including hemorrhage, odynophagia, damage to teeth, taste disorders, atlantoaxial subluxation, lingual edema, infection, and injury of the carotid artery. Pneumomediastinum, pneumopericardium, and epidural pneumatosis are an extremely unusual condition in children with adenotonsillectomy. Treatment should be conservative in the majority of cases and based on benign self-limiting course of these diseases; early recognition can prevent further complications. The combination of pneumomediastinum with epidural pneumatosis, pneumopericardium, retropharyngeal-prevertebral pneumatosis, axillar-perihumeral pneumatosis, and subcutaneous emphysema is also a very rare condition. We present a unique case with the radiological findings of air in all of these areas in a 6-year-old male child with adenotonsillectomy. The case was unusual in that the patient developed this complication 3 hours later after adenotonsillectomy with severe vomitting. The possible mechanism, the algorithm of treatment, and precautions in such cases will be discussed.

scholarly journals Pneumomediastinum, pneumopericardium, and subcutaneous emphysema—a rare complication in COVID-19 infection

2021 ◽  
Vol 15 (1) ◽  
Author(s):  
Archana Baburao ◽  
Rinki Das ◽  
Shylaja Shyamsunder
Keyword(s):  
Subcutaneous Emphysema ◽  
Early Recognition ◽  
Rare Complication ◽  
Public Health Problem ◽  
Rare Condition ◽  
Prognostic Indicator ◽  
Case Presentation ◽  
Spontaneous Pneumomediastinum ◽  
Global Pandemic ◽  
Almost All

Abstract Background Coronavirus disease 2019 (COVID-19) has become a global pandemic and is posing a serious public health problem for almost all countries. Spontaneous pneumomediastinum, a rare condition, is usually seen in patients with underlying pulmonary pathology, infections, or mechanical ventilation. Spontaneous pneumomediastinum is a rare complication in COVID-19 pneumonia. Case presentation We report a case of spontaneous pneumomediastinum, pneumopericardium, and subcutaneous emphysema in a 62-year-old diabetic patient with COVID-19 infection who presented with cough, fever, and breathlessness, which turned to be a fatal complication. Conclusion Pneumomediastinum/subcutaneous emphysema, a not so common complication associated with COVID-19 infection, should be considered as a bad prognostic indicator of worsening disease and hence requires early recognition and careful monitoring of the patient for any possible unfavorable outcome.

scholarly journals Hamman’s syndrome: spontaneous pneumomediastinum and subcutaneous emphysema during second stage of labour

2017 ◽  
Vol 6 (6) ◽  
pp. 2622
Author(s):  
Ying Yiing Lou
Keyword(s):  
Subcutaneous Emphysema ◽  
Early Recognition ◽  
Rare Complication ◽  
Anterior Chest Wall ◽  
Second Stage ◽  
Second Stage Of Labour ◽  
Chest X Ray ◽  
Surgical Emphysema ◽  
Future Pregnancy ◽  
Limiting Condition

Subcutaneous emphysema with pneumomediastinum in labour is also known as Hamman's Syndrome. Maternal pneumomediastinum associated with subcutaneous emphysema is a rare complication of pregnancy. The incidence rate being between 1:2000 and 1:10,000. Pneumomediastinum occurs most frequently in the second stage of labour in a healthy primiparous women with prolonged labour. A 29-year-old primigravida, who had no relevant medical history, had an uneventful spontaneous vaginal delivery at term. She used Entonox as analgesia in labour. She developed facial and neck oedema associated with mild breathing discomfort towards the end of her second stage. Crepitus was felt in her cheek, neck and anterior chest wall. Observations were stable including oxygen saturation. Chest X-ray demonstrated gross and extensive surgical emphysema across the chest and up into the neck and with no evidence of pneumothorax. She was managed conservatively and the subcutaneous emphysema was found to have considerably better within 24 hours. She recovered uneventfully and was discharged within 3 days of admission. A future pregnancy is planned. Hamman’s syndrome is generally a self-limiting condition. The key to successful management is early recognition followed by appropriate measures to prevent further complications in order to reduce the morbidity and mortality associated with this condition. Supportive measures alone may be the only requirement for resolution. Recurrence of the condition is rare but the appropriate management of subsequent pregnancies is unclear. Our case was appropriately managed with multidisciplinary input in the HDU on labour ward.

scholarly journals Tracheal Necrosis and Surgical Emphysema: A Rare Complication of Thyroidectomy

2002 ◽  
Vol 81 (10) ◽  
pp. 738-741 ◽  
Author(s):  
Edward W.H. To ◽  
W.M. Tsang ◽  
Michael D. Williams ◽  
Eric C.H. Lai ◽  
Matthew Chan
Keyword(s):  
Subcutaneous Emphysema ◽  
Rare Complication ◽  
Rare Condition ◽  
Trapped Air ◽  
Surgical Emphysema

We describe the first reported case of tracheal necrosis following a thyroidectomy. This complication resulted in massive subcutaneous emphysema and pneumomediastinum. which required emergency exploration of the neck to decompress the trapped air. We also discuss the suggested etiology and management of this rare condition.

scholarly journals A case of acute compartment syndrome of the hand complicating subcutaneous emphysema due to accidental nitrogen gas insufflation

2019 ◽  
Vol 27 (1) ◽  
pp. 81-84
Author(s):  
Collin SK Looi ◽  
Manohar Arumugam
Keyword(s):  
Compartment Syndrome ◽  
Current Literature ◽  
Subcutaneous Emphysema ◽  
Surgical Intervention ◽  
Rare Condition ◽  
Acute Compartment Syndrome ◽  
Potential Complication ◽  
Nitrogen Gas ◽  
Unique Case

Non-infectious subcutaneous emphysema of the hand has previously been mentioned in literature. In most cases, it presents in a benign and self-resolving form, which may be managed conservatively. However, in cases of subcutaneous emphysema involving insufflation with nitrogen gas, clinical vigilance is advised as acute compartment syndrome may be a potential complication due to the non-permeative nature of the gas. This would necessitate a complete change in the dynamics of management, warranting urgent surgical intervention. Current literature on acute compartment syndrome of the hand complicating subcutaneous emphysema is scarce. This report aims to highlight this unique case and add to the current literature on this rare condition.

scholarly journals Presentation of pulmonary tuberculosis and actinomyces co-infection as a lung mass: a literature review and unique case report

2019 ◽  
Vol 89 (3) ◽  
Author(s):  
Evangelos Balis ◽  
Sotiris Kakavas ◽  
Steven Kompogiorgas ◽  
Konstantinos Kotsifas ◽  
Georgios Boulbasakos
Keyword(s):  
Surgical Intervention ◽  
Clinical Symptoms ◽  
Rare Condition ◽  
Radiological Findings ◽  
Unique Case ◽  
The Past ◽  
Lung Malignancy ◽  
Pulmonary Actinomycosis ◽  
Lung Infections ◽  
Parenchymal Lung

Parenchymal lung infections occasionally present with clinical symptoms and radiological findings similar to lung malignancy. Pulmonary actinomycosis is a rare condition of its own right, let alone in coexistence with tuberculosis. We report a case of a man presenting with hemoptysis alongside a chest computed tomography compatible with lung cancer. The diagnosis, after removal of a large endobronchial mass with flexible bronchoscopy and cryon, was a concomitant infection with Mycobacterium tuberculosis and Actinomyces odontoliticus. In the literature, there are few reported cases with concomitant tuberculosis and actinomycosis. To our knowledge, such radical treatment without surgical intervention has not been reported in the past.

scholarly journals Hemoperitoneum Secondary to Spontaneous Rupture of a Retroperitoneal Varix

2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Derrick D. Eichele
Keyword(s):  
Abdominal Pain ◽  
Clinical Presentation ◽  
Surgical Intervention ◽  
Acute Abdominal Pain ◽  
Early Recognition ◽  
Relevant Literature ◽  
Hypovolemic Shock ◽  
Rare Condition ◽  
Unique Case ◽  
Life Threatening

Hemoperitoneum due to a ruptured retroperitoneal varix is an exceedingly rare condition and a poor prognostic sign with catastrophic and life-threatening complication of portal hypertension. We present a unique case of a 56-year-old female with cirrhosis secondary to primary sclerosing cholangitis who presented with acute abdominal pain and hypovolemic shock prior to a cardiac arrest following a ruptured retroperitoneal varix without prior esophageal varices and a newly identified intrahepatic cholangiocarcinoma. The clinical presentation with abdominal pain and hemorrhagic shock is consistently reported in the relevant literature. Early recognition affords appropriate management and urgent surgical intervention leading to survival.

Pseudoaneurysm of the left internal carotid artery following tonsillectomy

VASA ◽  
2011 ◽  
Vol 40 (6) ◽  
pp. 491-494 ◽  
Author(s):  
Vávrová ◽  
Slezácek ◽  
Vávra ◽  
Karlová ◽  
Procházka
Keyword(s):  
Carotid Artery ◽  
Internal Carotid Artery ◽  
Internal Carotid ◽  
Rare Complication ◽  
Left Internal Carotid Artery ◽  
Acute Tonsillitis ◽  
Artery Pseudoaneurysm ◽  
Complete Occlusion ◽  
Endovascular Approach ◽  
Deep Neck Infections

Internal carotid artery pseudoaneurysm is a rare complication of deep neck infections. The authors report the case of a 17-year-old male who presented to the Department of Otorhinolaryngology with an acute tonsillitis requiring tonsillectomy. Four weeks after the surgery the patient was readmitted because of progressive swallowing, trismus, and worsening headache. Computed tomography revealed a pseudoaneurysm of the left internal carotid artery in the extracranial segment. A bare Wallstent was implanted primarily and a complete occlusion of the pseudoaneurysm was achieved. The endovascular approach is a quick and safe method for the treatment of a pseudoaneurysm of the internal carotid artery.

Free-Floating Thrombus in the Distal Internal Carotid Artery Causing a Stroke

2020 ◽  
Author(s):  
Spyros Papadoulas ◽  
Konstantinos Moulakakis ◽  
Natasa Kouri ◽  
Petros Zampakis ◽  
Stavros K. Kakkos
Keyword(s):  
Carotid Artery ◽  
Internal Carotid Artery ◽  
Medical Management ◽  
Internal Carotid ◽  
Treatment Strategies ◽  
Rare Condition ◽  
Residual Stenosis ◽  
Floating Thrombus ◽  
Distal Internal Carotid Artery ◽  
Carotid Bulb

AbstractWe present a patient suffering from a stroke with a free-floating thrombus extending up to the distal internal carotid artery. The thrombus was totally resolved after a 2-week anticoagulation regimen without leaving behind any severe residual stenosis in the carotid bulb. The optimal treatment of this rare condition remains uncertain. We report some important treatment strategies that have been used in the literature, emphasizing the anticoagulation as the mainstay of therapy. Immediate surgical and interventional manipulations carry the risk of thrombus dislodgement and embolization and should be considered if there are recurrent symptoms despite medical management.

Intraorbital Abscess: A Rare Cause of Orbit Compression

FACE ◽  
2021 ◽  
pp. 273250162110050
Author(s):  
Samuel Ruiz ◽  
Rizal Lim
Keyword(s):  
Pediatric Population ◽  
Rare Complication ◽  
Disease Process ◽  
Rare Condition ◽  
External Drainage ◽  
Direct Extension ◽  
Life Threatening ◽  
History Of ◽  
High Index Of Suspicion ◽  
Prompt Diagnosis

Introduction: Intraorbital abscess is a rare complication of rhinosinusitis that affects most commonly the pediatric population. It is thought to be caused by direct extension or venous spread of infections from contiguous sites and can lead to life-threatening complications, like permanent visual loss and cerebral abscesses. Objectives: Intraorbital abscess is a rare condition that requires prompt diagnosis and treatment to avoid serious complications. Our objectives are to provide an overview of this rare disease process and its management including our successful treatment experience. Case Description: We present a 2 case report of a 13-year-old pediatric male and a 66-year-old male with history of chronic sinusitis who presented with a right intraorbital abscess successfully treated with external drainage with decompression of the orbit. Conclusion: When intraorbital abscess is encountered, a high index of suspicion is needed to allow prompt and accurate diagnosis for this infrequent condition. Timely surgical drainage of the abscess is needed to prevent the development of fatal complications.

A rare complication with Edwards Sapien: Aortic valve embolization in TAVI

Vascular ◽  
2014 ◽  
Vol 23 (1) ◽  
pp. 102-104 ◽  
Author(s):  
Hüseyin Ayhan ◽  
Tahir Durmaz ◽  
Telat Keleş ◽  
Hacı Ahmet Kasapkara ◽  
Kemal Eşref Erdoğan ◽  
...  
Keyword(s):  
Aortic Valve ◽  
Carotid Artery ◽  
Transcatheter Aortic Valve Implantation ◽  
Common Carotid Artery ◽  
Rare Complication ◽  
Transcatheter Aortic Valve ◽  
Truncus Brachiocephalicus ◽  
Edwards Sapien ◽  
Aortic Valve Implantation ◽  
Valve Implantation

One of the problems is valve embolization at the time of transcatheter aortic valve implantation, which is a rare but serious complication. In this case, we have shown balloon expandable aortic valve embolization TAVI which is a rare complication and we managed with second valve without surgery. Although there is not enough experience in the literature, embolized valve was re-positioned in the arch aorta between truncus brachiocephalicus and left common carotid artery.

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