1.Radiofrequency Catheter Ablation of Hemodynamically Unstable Ventricular Tachycardia Associated with Systemic Sclerosis.
Hoe Hoon CHUNG ; Jin Bae KIM ; Sung Hoon HONG ; Hong Joo LEE ; Boyoung JOUNG ; Moon Hyoung LEE
Journal of Korean Medical Science 2012;27(2):215-217
Systemic sclerosis (SS) is a connective tissue disease and cardiac involvement is common. Primary cardiac involvement such as conduction system disturbances and arrhythmias can also occur. However, reports of sustained ventricular tachycardia (VT) are rare. We report a case of catheter ablation of sustained ventricular tachycardia in a patient with systemic sclerosis using a conventional mapping system. A 64-yr-old woman with a 10-yr history of SS was referred for management of her ventricular tachycardia. There was no structural abnormality in cardiac chambers. However, electrophysiologic study revealed electrical substrate of ventricular tachycardia which could be ablated with pacemapping and substrate mapping. This case demonstrated successful conventional mapping and catheter ablation in a hemodynamically unstable patient with SS.
*Catheter Ablation
;
Electrocardiography
;
Female
;
Humans
;
Middle Aged
;
Scleroderma, Systemic/*complications/*diagnosis
;
Tachycardia, Ventricular/*etiology/physiopathology/*surgery
2.A Case of Mallory-Weiss Syndrome Complicating Pregnancy in a Patient with Scleroderma.
Kyu Hyun CHO ; Seong Wook HEO ; Seung Hie CHUNG ; Chae Gi KIM ; Ho Gak KIM ; Jung Yoon CHOE
The Korean Journal of Internal Medicine 2003;18(4):238-240
The majority of patients with scleroderma have gastrointestinal involvement, and a few experience gastrointestinal hemorrhage, however, gastrointestinal hemorrhage due to Mallory-Weiss syndrome is very rare. We report upon a 24-year-old pregnant woman with scleroderma who had gastrointestinal hemorrhage due to Mallory-Weiss syndrome.
Adult
;
Female
;
Gastrointestinal Hemorrhage/diagnosis/*etiology
;
Human
;
Mallory-Weiss Syndrome/*diagnosis/*etiology
;
Pregnancy
;
Pregnancy Complications/*diagnosis
;
Scleroderma, Systemic/*complications
3.Scleroderma-like Manifestation in a Patient with Primary Systemic Amyloidosis: Response to High-dose Intravenous Immunoglobulin and Plasma Exchange.
Sung Bin CHO ; Jun Su PARK ; Hyun Ok KIM ; Kee Yang CHUNG
Yonsei Medical Journal 2006;47(5):737-740
A 54-year-old Korean male with scleroderma-like manifestation of primary systemic amyloidosis presented with firm cutaneous induration of face and distal extremities, subcutaneous induration of the trunk and proximal extremities, limited range of motion in all joints, hoarseness, and dysphagia. Monthly high-dose intravenous immunoglobulin (hdIVIg) was given (three treatments, each time administering 0.4 g/kg per day for five days), and both signs and symptoms began to improve. However, the quantitative analyses of serum protein did not improve. Therapeutic plasma exchange (TPE) was performed monthly to clear the elevated serum immunoglobulin, and after several treatments, their levels normalized and symptoms were maintained in the improved state for more than two years. To summarize, hdIVIg and TPE combination therapy may be used as a safe first-line treatment for patients with primary systemic amyloidosis presenting with symptomatic monoclonal gammopathy.
Scleroderma, Systemic/diagnosis/etiology/*therapy
;
*Plasma Exchange
;
Middle Aged
;
Male
;
Immunoglobulins, Intravenous/administration & dosage/*therapeutic use
;
Humans
;
Combined Modality Therapy
;
Amyloidosis/*complications
4.Liver Cirrhosis Due to Autoimmune Hepatitis Combined with Systemic Sclerosis.
Byung Chul YOU ; Soung Won JEONG ; Jae Young JANG ; So Mi GOO ; Sang Gyune KIM ; Young Seok KIM ; Chan Hong JEON ; Yoon Mi JEEN
The Korean Journal of Gastroenterology 2012;59(1):48-52
Systemic sclerosis (SSc) is a chronic systemic disease that affects the skin, lungs, heart, gastrointestinal tract, kidneys, and musculoskeletal system. Although up to 90% of patients with scleroderma have been estimated to have gastrointestinal involvement, liver disease has been reported only rarely. A 51-year-old woman was hospitalized due to esophageal variceal bleeding. Her serum was positive for anti-nuclear antibody and anti-centromere antibody. Sclerodactyly was noted on both hands, and she had recently developed Raynaud's syndrome. Punch biopsy of the hand showed hyperkeratosis, regular acanthosis, and increased basal pigmentation in the epidermis, and thick pale collagenous bundles in the dermis. Liver biopsy showed chronic active hepatitis with bridging fibrosis. Consequently, she was diagnosed with liver cirrhosis due to autoimmune hepatitis (AIH) combined with SSc. AIH had subsided after administration of prednisolone at 40 mg per day. She received 5-10 mg/day of prednisolone as an outpatient, and her condition has remained stable. Patients with either AIH or SSc should be monitored for further development of concurrent autoimmune diseases. The early diagnosis of AIH combined with SSc will be helpful in achieving optimal management.
Anti-Inflammatory Agents/therapeutic use
;
Antibodies, Antinuclear/blood
;
Esophageal and Gastric Varices
;
Female
;
Gastrointestinal Hemorrhage
;
Hepatitis, Autoimmune/complications/*diagnosis/drug therapy
;
Humans
;
Liver Cirrhosis/*diagnosis/etiology/pathology
;
Middle Aged
;
Prednisolone/therapeutic use
;
Raynaud Disease/diagnosis
;
Scleroderma, Systemic/complications/*diagnosis
;
Skin/pathology
5.Intracranial Vasculopathy in a Patient with Systemic Sclerosis: Atherosclerotic or Moyamoya-Like Disease?.
Han Na CHOI ; Si Hye KIM ; Hyun Hee KIM ; Seong Kyu KIM ; Jung Yoon CHOE ; Sung Hoon PARK
The Korean Journal of Internal Medicine 2012;27(2):239-242
No abstract available.
Angiography, Digital Subtraction
;
Cerebral Angiography
;
Cerebrovascular Circulation
;
Collateral Circulation
;
Female
;
Humans
;
Infarction, Middle Cerebral Artery/diagnosis/*etiology/physiopathology
;
Intracranial Arteriosclerosis/diagnosis/*etiology/physiopathology
;
Magnetic Resonance Angiography
;
Middle Aged
;
Moyamoya Disease/diagnosis/*etiology/physiopathology
;
Predictive Value of Tests
;
Scleroderma, Systemic/*complications
;
Tomography, Emission-Computed, Single-Photon