Catastrophic congenital hemangioma with severe coagulopathy leading to fatal cardiac failure: Case report and review

2021 ◽  
Author(s):  
Sally Cohen‐Cutler ◽  
Linda J. Szymanski ◽  
Crystal Bockoven ◽  
Joseph M. Miller ◽  
Diana Moke ◽  
...  
Keyword(s):  
Case Report ◽  
Cardiac Failure ◽  
Congenital Hemangioma ◽  
Severe Coagulopathy

Congenital hemangioma with milialike structures: a case report.

1998 ◽  
Vol 15 (4) ◽  
pp. 307-308 ◽  
Author(s):  
A Rositto ◽  
S Avila ◽  
C Carames ◽  
R Drut
Keyword(s):  
Case Report ◽  
Congenital Hemangioma

scholarly journals EP09.03: Prenatal diagnosis of a voluminous facial rapidly involuting congenital hemangioma (RICH): a case report

2017 ◽  
Vol 50 ◽  
pp. 294-294
Author(s):  
A. Labrecque ◽  
J. Dubois ◽  
V. Moramarco ◽  
S. Wavrant
Keyword(s):  
Case Report ◽  
Prenatal Diagnosis ◽  
Congenital Hemangioma ◽  
Rapidly Involuting Congenital Hemangioma

Epithelioid hemangioendothelioma after radiotherapy for congenital hemangioma: a case report

2009 ◽  
Vol 27 (1) ◽  
pp. 130-133 ◽  
Author(s):  
Rui Niimi ◽  
Akihiko Matsumine ◽  
Katsuyuki Kusuzaki ◽  
Ken Shintani ◽  
Tomoki Nakamura ◽  
...  
Keyword(s):  
Case Report ◽  
Epithelioid Hemangioendothelioma ◽  
Congenital Hemangioma

HEMANGIOMA OF THE LIVER WITH HEART FAILURE: A CASE REPORT

PEDIATRICS ◽  
1954 ◽  
Vol 14 (2) ◽  
pp. 117-121
Author(s):  
ROBERT W. WINTERS ◽  
SAUL J. ROBINSON ◽  
GEORGE BATES
Keyword(s):  
Heart Failure ◽  
Congenital Heart Disease ◽  
Heart Disease ◽  
Case Report ◽  
Cardiac Hypertrophy ◽  
Cardiac Failure ◽  
Congenital Heart ◽  
Signs And Symptoms ◽  
Post Mortem ◽  
Great Vessels

A case of multiple hemangiomata of the liver is reported in an infant who presented signs and symptoms strongly suggesting congenital heart disease. The post mortem examination revealed no gross anomalies of the heart or great vessels, but did show a heart with cardiac hypertrophy. A mechanism to explain the cardiac failure in this case is discussed.

scholarly journals Severe coagulopathy and transient hypertension following a Rhabdophis subminiatus bite: a case report

2016 ◽  
Vol 49 (4) ◽  
pp. 520-522 ◽  
Author(s):  
Erni Juwita Nelwan ◽  
Randy Adiwinata ◽  
Siti Handayani ◽  
Ikhwan Rinaldi
Keyword(s):  
Case Report ◽  
Severe Coagulopathy

scholarly journals Congenital Hemangioma: A Case Report of a Finding Every Physician Should Know

Cureus ◽  
2018 ◽  
Author(s):  
Kamleshun Ramphul ◽  
Stephanie G Mejias ◽  
Yogeshwaree Ramphul-Sicharam ◽  
Ruhi Sonaye
Keyword(s):  
Case Report ◽  
Congenital Hemangioma

scholarly journals Ruptured aneurysm of right sinus of valsalva - a case report

2016 ◽  
Vol 44 (3) ◽  
pp. 175-177
Author(s):  
Md Nazmul Hasan ◽  
Md Nazmul Hasan ◽  
Md Harisul Hoque ◽  
SM Mustafa Zaman ◽  
Md Rasul Amin ◽  
...  
Keyword(s):  
Case Report ◽  
Cardiac Failure ◽  
Annulus Fibrosus ◽  
Common Complication ◽  
Sinus Of Valsalva ◽  
Sinus Of Valsalva Aneurysm ◽  
Aortic Media ◽  
Surgical Options ◽  
Potential Risks ◽  
The Right

The sinus of valsalva aneurysm (SVA) is a small dilatation caused by a separation between the aortic media and annulus fibrosus. It may be either acquired or congenital. The right coronary sinus is most frequently affected, with the most common complication being rupture of the sinus. Cardiac failure and sudden auscultation changes suggest the possibility of SVA rupture. Echocardiography is sufficient to diagnose SVA, its complications, repercussions and to determine surgical options. SVA, even if asymptomatic, has potential risks of expansion, rupture, cardiac failure, endocarditis, embolism and sudden death. This justifies surgical correction which has a low mortality rate in both the short and long-term.Bangladesh Med J. 2015 Sep; 44 (3): 175-177

scholarly journals Case report of amniotic fluid embolism coagulopathy following abortion; use of viscoelastic point-of-care analysis

2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Halley P. Crissman ◽  
Charisse Loder ◽  
Carlo Pancaro ◽  
Jason Bell
Keyword(s):  
Case Report ◽  
Amniotic Fluid ◽  
Point Of Care ◽  
Healthy Woman ◽  
Induced Abortion ◽  
Amniotic Fluid Embolism ◽  
Case Presentation ◽  
Induced Abortions ◽  
Life Threatening ◽  
Severe Coagulopathy

Abstract Background Amniotic fluid embolism (AFE) is a rare, life threatening obstetric complication, often associated with severe coagulopathy. Induced abortions are extremely safe procedures however complications including AFE can occur. Case presentation A 29-year-old previously healthy woman, gravida 1 para 0, presented for a scheduled second trimester induced abortion via dilation and evacuation at 22-weeks gestation. The case was complicated by a suspected AFE with associated profound coagulopathy. Viscoelastic point-of-care coagulation analysis was used to successfully and swiftly guide management of her coagulopathy. Conclusion AFE can occur in the setting of induced abortion. This case report suggests viscoelastic point-of-care coagulation analyzers may aid in the management of pregnancy-related coagulopathy by providing faster coagulation assessment than laboratory testing, and facilitating timely, targeted management of coagulopathy.

Prenatally diagnosed congenital hemangioma with elevated middle cerebral artery peak systolic velocity mimicking the Kasabach‐Merritt phenomenon: A case report

2019 ◽  
Vol 45 (12) ◽  
pp. 2456-2460
Author(s):  
Masayuki Someya ◽  
Jun Sasahara ◽  
Satoshi Yamamoto ◽  
Akihisa Sawada ◽  
Masanori Nishikawa ◽  
...  
Keyword(s):  
Case Report ◽  
Middle Cerebral Artery ◽  
Cerebral Artery ◽  
Peak Systolic Velocity ◽  
Congenital Hemangioma

scholarly journals SVT and Gram Negative Sepsis in Neonates

2019 ◽  
Vol 39 (3) ◽  
pp. 197-199
Author(s):  
Om Krishna Pathak ◽  
Yengkhom Rameshwor Singh ◽  
Sunil Purswani ◽  
Pradeep Suryawanshi
Keyword(s):  
Heart Rate ◽  
Case Report ◽  
Supraventricular Tachycardia ◽  
Cardiac Failure ◽  
Neonatal Sepsis ◽  
Congestive Cardiac Failure ◽  
Gram Negative ◽  
Neonates And Infants ◽  
Culture Positive ◽  
Insight Into

Supraventricular tachycardia is the most common tachyarrhythmia seen in fetuses, neonates and infants. Sustained SVT may lead to congestive cardiac failure. Neonatal supraventricular tachycardia is more commonly associated with other cardiorespiratory and congenital problems and is uncommon in an otherwise healthy infant. Supraventricular tachycardia is also caused by neonatal sepsis but has rarely been reported. Here, we report two cases of SVT (Supraventricular tachycardia) induced by neonatal sepsis. Two neonates, one male and another female, both born to Indian mother had tachycardia with heart rate > 220 beats/minute along with poor perfusion, tachypnoea, fever and deranged coagulation profile. Both the babies had culture positive gram negative sepsis with normal echocardiography and supraventricular tachycardia on electrocardiograms which were treated with anti arrhythmic drugs and treatment of sepsis. This case report gives further insight into one more presentation and complication of neonatal sepsis.

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