1.A case of Budd-Chiari syndrome with high antiphospholipid antibody in a patient with systemic lupus erythematosus.
Yeoun Yeon YUN ; Kyung Ah YOH ; Hyoung In YANG ; Sung Hwan PARK ; Sang Heon LEE ; Chul Soo CHO ; Ho Youn KIM
The Korean Journal of Internal Medicine 1996;11(1):82-86
Antiphospholipid syndrome is characterized by recurrent episodes of arterial and venous thrombosis, spontaneous fetal losses, thrombocytopenia and persistently elevated levels of antiphospholipid antibodies. We experienced a case of Budd-Chiari syndrome in a 32-year old female lupus patient who was presented with left leg edema, ascites and esophageal varix. The clinical and laboratory findings were compatible with the cirteria for systemic lupus erythematosus (SLE) and she was found to have anticardiolipin antibody, thrombocytopenia and prolonged partial thromboplastin time. Initially, she was treated with intravenous heparin and uroki nase and she was followed up with warfarin, baby aspirin and steroids.
Adult
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Angiography
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Animal
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Antibodies, Antiphospholipid/blood*
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Case Report
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Drug Therapy, Combination
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Female
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Hepatic Vein Thrombosis/complications
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Hepatic Vein Thrombosis/diagnosis*
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Hepatic Vein Thrombosis/drug therapy
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Human
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Lupus Erythematosus, Systemic/complications
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Lupus Erythematosus, Systemic/diagnosis*
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Lupus Erythematosus, Systemic/drug therapy
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Tomography, X-Ray Computed
2.Clinical and Imaging Findings of Neonatal Seizures Presenting as Diffuse Cerebral White Matter Abnormality on Diffusion-Weighted Imaging without any Structural or Metabolic Etiology
Maeran KIM ; Jae-Yeon HWANG ; Yeoun Joo LEE ; Yong-Woo KIM ; Shin Yun BYUN ; Yun-Jin LEE ; Jeong A YEOM ; Ung Bae JEON ; Ki Seok CHOO ; Kyung Jin NAM ; Storm Nicholas SHAUN REID
Journal of the Korean Radiological Society 2020;81(6):1412-1423
Purpose:
Some patients with neonatal seizures show diffuse, symmetric diffusion-restricted lesions in the cerebral white matter. The aim of this study was to describe clinical and imaging findings of patients with neonatal seizures who had diffuse, symmetric diffusion-restricted lesions without any structural or metabolic etiology.
Materials and Methods:
A total of 56 neonates aged less than 1 week underwent brain magnetic resonance imaging (MRI) for evaluation of seizures from November 2008 to February 2017. After excluding 43 patients, 13 patients showed diffuse white matter abnormality on diffusion-weighted imaging. Initial and follow-up clinical and MRI findings were analyzed retro-spectively.
Results:
All 13 patients were born at full term. Among the ten patients who underwent a stool test for viruses, six were positive for rotavirus and one for astrovirus. MRI revealed diffuse, symmetric diffusion-restricted lesions distributed along the cerebral white matter, thalami, and midbrain variably.
Conclusion
Diffuse, symmetric diffusion-restricted lesions involving the cerebral white matter can be seen in patients with neonatal seizures without any structural or metabolic etiology. Rotavirus is commonly but not exclusively detected in these patients. Nevertheless, viral infection-associated encephalopathy should be considered for patients with characteristic clinical and MRI findings.