1.Cerebral venous thrombosis in an adult patient with nephrotic syndrome.
Luhua WEI ; Yang LIU ; Yining HUANG
Chinese Medical Journal 2014;127(18):3354-3355
2.Diagnosis and treatment of mesenteric venous thrombosis early after operation.
Kai PAN ; Li-gang XIA ; Xiao-chun CHEN ; Ke-li ZHONG ; Hou-xiang JIANG
Chinese Journal of Gastrointestinal Surgery 2005;8(1):50-52
OBJECTIVETo analyze the clinical characteristics diagnosis and treatment of patients with mesenteric venous thrombosis early after operation.
METHODSA retrospective study was performed on the clinical data of 7 patients with mesenteric venous thrombosis early after operation from 1990 to 2004.
RESULTSPatients had main clinical manifestations of severe abdominal pain and vomiting, but abdominal signs were slight. The systemic toxic symptoms occurred in 2 cases at late course. The examination of abdominal X- ray showed intestinal obstruction of all patients. Four patients received abdominal CT- scanning, of whom 3 patients were diagnosed as mesenteric venous thrombosis. Seven patients received exploratory operation. The necrotic intestinal segments were resected. Two patients had short intestinal syndromes after operation, one of them died of serious malnutrition. Four patients who had recurrence of portal, mesenteric and iliac venous thrombosis needed a long-term therapy of warfarin and aspirin after discharge.
CONCLUSIONIt is easy to make a mistake in diagnosis because of the lacking of characteristic clinical manifestations. Exploratory operation immediately plus anticoagulant therapy is strongly recommended.
Adult ; Female ; Humans ; Male ; Mesenteric Vascular Occlusion ; diagnosis ; drug therapy ; etiology ; Middle Aged ; Postoperative Complications ; diagnosis ; drug therapy ; Retrospective Studies ; Thrombolytic Therapy ; Venous Thrombosis ; diagnosis ; drug therapy ; etiology
3.Blood-stasis and toxin causing catastrophe hypothesis and acute cardiovascular events: proposal of the hypothesis and its clinical significance.
Hao XU ; Da-Zhu SHI ; Hui-Jun YIN
Chinese Journal of Integrated Traditional and Western Medicine 2008;28(10):934-938
A hypothesis of " blood-stasis and toxin causing catastrophe engender acute cardiovascular event (ACE)" was put forward according to TCM cognition on blood-stasis and toxin, in combining with the up to date concept of atherosclerosis and coronary heart disease, and together with our clinical practical experiences. The etiology, pathogenesis, evolving law, initial characteristics, clinical manifestation, therapeutic methods, prescriptions and their compatibility, as well as the well-suited time for applying TCM intervention were discussed. The authors stressed that it is of great significance for further reducing the morbidity of ACE and improving the effect of integrative medicine for preventing and treating cardiovascular thrombotic disease.
Acute Disease
;
therapy
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Cardiovascular Diseases
;
diagnosis
;
drug therapy
;
etiology
;
Coronary Thrombosis
;
complications
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Drugs, Chinese Herbal
;
administration & dosage
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Humans
5.Spontaneous perforation and dissection of the sinus of Valsalva and interventricular septum with intracardiac thrombus in a patient with Behcet's disease.
Yoon Jung JANG ; Jun Young KIM ; Kyung Been LEE ; Gun Wung NA ; Won Jae LEE ; Won Il PARK ; Mirae LEE
The Korean Journal of Internal Medicine 2015;30(2):252-255
No abstract available.
Aneurysm, Dissecting/diagnosis/*etiology/physiopathology/therapy
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Anticoagulants/therapeutic use
;
Aortic Aneurysm/diagnosis/*etiology/physiopathology/therapy
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Behcet Syndrome/*complications/diagnosis/drug therapy
;
Cerebral Infarction/diagnosis/etiology
;
Diffusion Magnetic Resonance Imaging
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Echocardiography, Doppler, Color
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Electrocardiography
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Hemodynamics
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Humans
;
Immunosuppressive Agents/therapeutic use
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Male
;
Middle Aged
;
*Sinus of Valsalva/physiopathology/ultrasonography
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Thrombosis/diagnosis/drug therapy/*etiology/physiopathology
;
Ventricular Septal Rupture/diagnosis/*etiology/physiopathology/therapy
6.A case of Behcet's disease with superior and inferior vena caval occlusion.
Wan Hee YOO ; Jin Seong MOON ; Sung Il KIM ; Wan Uk KIM ; Jun Gi MIN ; Sung Hwan PARK ; Sang Heon LEE ; Chul Soo CHO ; Ho Yeon KIM
The Korean Journal of Internal Medicine 1998;13(2):136-139
Behcet's disease is a chronic multisystemic disorder involving many organs and characterized by recurrent oral and genital ulcers and relapsing iritis. A case of BD with large vein thrombosis involving superior and inferior vena cava is presented. Large vein thrombosis in BD is not commonly developed and most commonly observed in the inferior or superior vena cava. A review of the literature emphasizes the rarity of the combined superior and inferior vena caval occlusion. Existence of extensive large vein occlusion in BD is associated with limited therapy and poor prognosis.
Adult
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Behcet's Syndrome/diagnosis
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Behcet's Syndrome/complications*
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Disease Progression
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Fatal Outcome
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Female
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Fibrinolytic Agents/therapeutic use
;
Human
;
Phlebography
;
Thrombosis/etiology*
;
Thrombosis/drug therapy
;
Thrombosis/diagnosis
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Vena Cava, Inferior/radiography*
;
Vena Cava, Superior/radiography*
;
Substances: Fibrinolytic Agents
7.Deep vein thrombosis associated with acute brucellosis: a case report and review of the literature.
Makram KOUBAA ; Makram FRIGUI ; Yousra CHERIF ; Moez JALLOULI ; Neila KADDOUR ; Mounir BEN JEMAA ; Zouheir BAHLOUL
The Korean Journal of Internal Medicine 2013;28(5):628-630
No abstract available.
Acute Disease
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Anti-Bacterial Agents/therapeutic use
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Anticoagulants/therapeutic use
;
Brucellosis/*complications/diagnosis/drug therapy/microbiology/transmission
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Humans
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Male
;
Middle Aged
;
Thrombophlebitis/etiology
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Treatment Outcome
;
Venous Thrombosis/diagnosis/drug therapy/*etiology
8.Clinical significance of antiphospholipid antibody in pediatric patients and review of literature.
Hui-Jie XIAO ; Ji-Yun YANG ; Tian-Ji GAO ; Jian-Ping HUANG ; Yong YAO ; Yan ZHANG
Chinese Journal of Pediatrics 2004;42(8):571-573
OBJECTIVEAntiphospholipid antibody (APL) is a particularly important laboratory diagnostic criterion for antiphospholipid syndrome (APS). The significances of positive APL in childhood are seldom reported nor fully understood. The purpose of this study was to analyze 13 cases with positive APL seen in our hospital and to study the relationship between the positive rates of APL and various clinical diseases especially systemic lupus erythematosus (SLE) in order to improve the clinical diagnoses and treatment level of APS in children.
METHODSThe clinical data collected from 2000 to 2002 of 13 hospitalized children with positive APL were retrospectively evaluated. Enzyme linked immunosorbent assay (ELISA) and indirect immunofluorescence technique were used respectively to detect APL and antineutrophil cytoplasmic autoantibodies (ANCA) of sera from those children. Other various indexes were also detected according to different characteristics of different diseases.
RESULTSEight cases had SLE; 2 had acute post-streptococcal infections. The other 3 cases did not show any evidences of primary diseases; they probably had primary APS. SLE was the most common primary diseases to cause development of APL and the cases with SLE showed more severe cutaneous vasculitis than SLE patients who were negative for APL. There was no significant relationship between the positive rates of APL and that of ANCA. Eight APL positive cases complicated with thrombocytopenia and bleeding were treated with high dosage of immunoglobulin [400 mg/(kg.d), for 3 - 5 d] intravenously; the clinical conditions of these cases were ameliorated soon. While the 5 cases who had thrombotic vasculitis and thromboembolism were treated with anticoagulant and antithrombotic therapy with low molecular weight heparin [50 - 100 U/(kg.d)], which led to good clinical effects.
CONCLUSIONSThe clinical manifestations of children positive for APL were somehow different from those of adults. Positive APL itself may be nonspecific, it can occur from different causes of diseases. APL detection may be useful to suggest anticoagulant and/or antithrombosis therapy. Treatments for APS should be variable according to different causes and severity of diseases, in the cases of thrombocytopenia and bleeding, high dose intravenous immunoglobulin should be given as soon as possible, while in the cases of thrombotic vasculitis and thromboembolism, anticoagulant and antithrombotic therapy should be given soon.
Adult ; Antibodies, Antineutrophil Cytoplasmic ; blood ; Antibodies, Antiphospholipid ; blood ; immunology ; Anticoagulants ; therapeutic use ; Antiphospholipid Syndrome ; blood ; complications ; diagnosis ; therapy ; Child ; Fibrinolytic Agents ; therapeutic use ; Hemorrhage ; etiology ; therapy ; Humans ; Immunoglobulins, Intravenous ; therapeutic use ; Lupus Erythematosus, Systemic ; immunology ; Streptococcal Infections ; immunology ; Thrombocytopenia ; etiology ; therapy ; Thromboembolism ; drug therapy ; etiology ; Thrombosis ; drug therapy ; etiology ; Vasculitis ; drug therapy ; etiology
10.Six Kawasaki disease patients with acute coronary artery thrombosis.
Shu-lai ZHOU ; Jian-ping LUO ; Yan-qi QI ; Yu-guang LIANG ; Wei WANG ; Fang-qi GONG
Chinese Journal of Pediatrics 2013;51(12):925-929
OBJECTIVETo improve the awareness of acute coronary artery thrombosis in Kawasaki disease (KD).
METHODSix KD patients with acute coronary artery thrombosis (Jan. 2004 to Jan. 2013) were studied retrospectively. The basic information, clinical manifestations, laboratory data, echocardiography and electrocardiography (ECG), method and consequence of thrombolytic therapy were analyzed.
RESULTThe mean age of patients with coronary artery thrombosis (5 males and 1 female) was (17.2 ± 11.3) months.Five cases had thrombosis in left coronary artery (LCA), and four cases had thrombosis in aneurysm of left anterior descending artery (LAD). One case had thrombosis in both left and right coronary artery (RCA).One case died. Maximum thrombus was about 1.60 cm × 0.80 cm, locating in LAD. The diameter of LCA and RCA was (0.44 ± 0.07) cm and (0.45 ± 0.07) cm. Two patients showed abnormal ECG. Case 3 showed ST segment depression in lead V5. Case 6 showed myocardial infarction.In acute phase of KD, three patients received treatment with intravenous immunoglobin (IVIG), five patients were treated with aspirin.In sub-acute and convalescent phase of KD, all patients were treated with low-dose aspirin.Warfarin and dipyridamole were applied in 5 patients. All cases were treated with thrombolytic therapy using urokinase and/or heparin. After thrombolytic therapy, echocardiography showed thrombolysis in four cases and no change in one.One patient died of myocardial infarction.
CONCLUSIONMost of acute coronary thrombosis in KD occurred in LAD. KD patients with coronary artery thrombosis are at risk of sudden death due to myocardial infarction.
Acute Disease ; Anticoagulants ; administration & dosage ; therapeutic use ; Aspirin ; administration & dosage ; therapeutic use ; Child, Preschool ; Coronary Aneurysm ; diagnosis ; drug therapy ; etiology ; Coronary Thrombosis ; diagnosis ; drug therapy ; etiology ; Echocardiography ; Electrocardiography ; Female ; Fibrinolytic Agents ; administration & dosage ; therapeutic use ; Humans ; Immunoglobulins, Intravenous ; administration & dosage ; therapeutic use ; Infant ; Infant, Newborn ; Male ; Mucocutaneous Lymph Node Syndrome ; complications ; drug therapy ; Myocardial Infarction ; diagnosis ; etiology ; mortality ; Retrospective Studies