Arterial thrombosis as clinical manifestation of congenital protein C deficiency

1991 ◽  
Vol 62 (5) ◽  
pp. 180-183 ◽  
Author(s):  
V. De Stefano ◽  
G. Leone ◽  
P. Micalizzi ◽  
L. Teofili ◽  
P. G. Falappa ◽  
...  
2017 ◽  
Vol 12 (1) ◽  
pp. 34-36
Author(s):  
Tunaggina Afrin Khan ◽  
Saiful Ahmed ◽  
Abu Sadique Abdullah ◽  
Mohammad Sarwar Alam ◽  
SM Eftarjahan Kabir ◽  
...  

Abstract not availableUniversity Heart Journal Vol. 12, No. 1, January 2016; 34-36


2019 ◽  
Vol 12 (7) ◽  
pp. e230034 ◽  
Author(s):  
Sanchari Chakravarty ◽  
Saugata Acharyya ◽  
Manas Kumar Mahapatra

A 9-day-old female baby presented with complaints of progressively worsening respiratory distress and lethargy. The parents were first cousins with history of multiple fetal losses in previous pregnancies. On examination, the baby was noted to be tachypnoeic, tachycardic with poor peripheral perfusion of the lower extremities. Femoral pulses on both sides were barely palpable. Echocardiography was normal. But cardiac catheterisation revealed the presence of an intraluminal obstruction of the distal aorta by a large thrombus. An attempt to dissolve the thrombus with urokinase infusion was unsuccessful. The affected vessels were then surgically explored and a large thrombus from the common iliac artery and distal abdominal aorta was removed. Following this, the child recovered uneventfully with return of lower limb pulsation. A thrombotic profile revealed the underlying diagnosis of congenital protein C deficiency responsible for the arterial thrombosis. This is an extremely unusual presentation, hardly ever been reported before.


1989 ◽  
Vol 61 (01) ◽  
pp. 144-147 ◽  
Author(s):  
A Girolami ◽  
P Simioni ◽  
A R Lazzaro ◽  
I Cordiano

SummaryDeficiency of protein S has been associated with an increased risk of thrombotic disease as already shown for protein C deficiency. Deficiencies of any of these two proteins predispose to venous thrombosis but have been only rarely associated with arterial thrombosis.In this study we describe a case of severe cerebral arterial thrombosis in a 44-year old woman with protein S deficiency. The defect was characterized by moderately reduced levels of total and markedly reduced levels of free protein S. C4b-bp level was normal. Protein C, AT III and routine coagulation tests were within the normal limits.In her family two other members showed the same defect. All the affected members had venous thrombotic manifestations, two of them at a relatively young age. No other risk factors for thrombotic episodes were present in the family members. The patient reported was treated with ASA and dipyridamole and so far there were no relapses.


1988 ◽  
Vol 29 (2) ◽  
pp. 120-121 ◽  
Author(s):  
Valerio de Stefano ◽  
Giuseppe Leone ◽  
Luciana Teofili ◽  
Rita Ferrelli ◽  
Giuseppe Pollari ◽  
...  

PEDIATRICS ◽  
1986 ◽  
Vol 77 (5) ◽  
pp. 670-676
Author(s):  
Patrick Yuen ◽  
Alfred Cheung ◽  
Hsiang Ju Lin ◽  
Faith Ho ◽  
Jun Mimuro ◽  
...  

Severe and recurrent purpura fulminans developed in a Chinese boy at one day of age. Results of coagulation studies performed on the patient during attacks were compatible with the diagnosis of disseminated intravascular coagulation. Subsequent investigations have revealed that the patient is homozygous and that his parents are heterozygous for protein C deficiency. Cryoprecipitate and fresh frozen plasma induced a remission, and administration of warfarin has been successful in preventing recurrence of attacks for as long as 8 months without infusion of any plasma components. None of the family members who are heterozygous for protein C deficiency have had thrombotic episodes.


2020 ◽  
Vol 27 (1) ◽  
pp. 100-103
Author(s):  
Kazuki Ueda ◽  
Eriko Morishita ◽  
Hironaga Shiraki ◽  
Shunzo Matsuoka ◽  
Shinsaku Imashuku

2019 ◽  
Vol 41 (4) ◽  
pp. e210-e215 ◽  
Author(s):  
Xiuli Yuan ◽  
Changgang Li ◽  
Xiaowen Chen ◽  
Liwei Liu ◽  
Guosheng Liu ◽  
...  

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