scholarly journals Peripheral venous malformations and pulmonary hypertension: A case report and literature review

2015 ◽  
Vol 3 (1) ◽  
pp. 101
Author(s):  
NambakamTanuja Subramanyam ◽  
Shashidaran ◽  
R Veena ◽  
GirishP Vakrani
2018 ◽  
Vol 12 (4) ◽  
pp. 202-204 ◽  
Author(s):  
CM McCarthy ◽  
M McCarthy ◽  
K O’Donoghue

The incidence of hepatocellular carcinoma in pregnancy is rare, and we present the first reported case of a pregnancy complicated by pre-existing advanced hepatocellular carcinoma. We describe the case of a 39-year-old woman in her second pregnancy, with a diagnosis of hepatocellular carcinoma. This was discovered in 2013 incidentally following hepato-splenectomy and pancreatectomy for a presumed hepatic adenoma in the context of multiple arterio-venous malformations. Recurrent hepatocellular carcinoma, in conjunction with co-existing pulmonary hypertension was successfully managed in a multi-disciplinary setting, resulting in a spontaneous vaginal delivery of a live female infant with maternal and neonatal survival six months following delivery.


2018 ◽  
Vol 8 (1) ◽  
pp. 71-75
Author(s):  
Anna Iacoi ◽  
Alexander Brobeil ◽  
Malena Götte ◽  
Christian Enzensberger ◽  
Vera Müller ◽  
...  

Abstract Pulmonary capillary haemangiomatosis (PCH) is a rare disorder of the lung, well described in adult literature. PCH is characterized by capillary proliferation, infiltrating the interstitium and alveolar walls. This leads to development of respiratory distress and to end-stage pulmonary hypertension. Mostly young adults are affected. The affection of newborn is described in less than ten cases in literature in the past forty years. PCH is a mostly deadly ending disease. We present a preterm born infant with antepartal diagnosed hydrops fetalis, who died 30 minutes after birth. Autopsy revealed PCH as lethal reason and not cardial disease as presumed before.


2009 ◽  
Vol 2009 (may13 1) ◽  
pp. bcr0620080095-bcr0620080095 ◽  
Author(s):  
P. L Lyle ◽  
R. D Weber ◽  
J. Bogarin ◽  
T. Kircher

2020 ◽  
Vol 2020 ◽  
pp. 1-5
Author(s):  
Mahmood Mubasher ◽  
Amir Hanafi ◽  
Tausif Syed ◽  
Abir Zinal ◽  
Ibrahim Y. Abubeker ◽  
...  

Postpartum pulmonary hypertension (PPPHT) is an extremely rare disorder, with few reported cases. Late diagnosis and treatment are associated with significant morbidity and mortality. We present an 18-year-old female patient who presented four-week postpartum with a typical submissive pulmonary embolism picture subsequently diagnosed as postpartum pulmonary hypertension. The patient had an excellent response to treatment, with a dramatic improvement in her functional status. The authors aim to urge physicians to keep this rare disorder in mind as timely and accurate diagnosis is crucial for management—additionally, the importance of counseling patients about the imminent risks associated with planned future pregnancies.


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