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1.
The Journal of the Korean Orthopaedic Association ; : 657-660, 2000.
Article in Korean | WPRIM | ID: wpr-652534

ABSTRACT

Vascular leiomyoma or angioleiomyoma is a uncommon benign solitary tumor that arises from the tunica muscularis of blood vessels. It is usually located in the wall of the uterus. It may present with a confusing picture of hand pain and paresthesia or be asymptomatic. We describe a 49-year-old man who presented with a slowly growing mass in the volar region of wrist which, on histological examination, was shown to be a vascular leiomyoma. It is not usually included in the differential diagnosis of anterior wrist mass or median nerve tumors.


Subject(s)
Humans , Middle Aged , Angiomyoma , Blood Vessels , Diagnosis, Differential , Hand , Leiomyoma , Median Nerve , Paresthesia , Uterus , Wrist
2.
The Journal of the Korean Orthopaedic Association ; : 259-264, 1999.
Article in Korean | WPRIM | ID: wpr-649045

ABSTRACT

Thyroid acropachy is a rare complication of Graves' disease, manifested by clubbing of the terminal phalanges, periosteal new bone formation and overlying soft tissue swelling, It may occur when the patient is hypothyroid, euthyroid or hyperthyroid. In most cases, it is a part of the syndrome, including exophthalmos and/or pretibial myxedema. The authors have experienced one case of thyroid acropachy and report with a review of the literature review. The patient a 56-year-old female with a characteristic feathery new bone formation on the medial side of the shaft of the left first metatarsal bone and overlying soft tissue swelling. However, there was no pretibial myxedema and clubbing of fingers. She was hypothyroid and treated with systemic corticosteroid for mild pain and persistent swelling. The treatment had temporarily improved the patient's condition.


Subject(s)
Female , Humans , Middle Aged , Exophthalmos , Fingers , Graves Disease , Metatarsal Bones , Myxedema , Osteogenesis , Thyroid Gland
3.
The Journal of the Korean Orthopaedic Association ; : 189-194, 1999.
Article in Korean | WPRIM | ID: wpr-650650

ABSTRACT

Legg-Calve-Perthes disease (LCP) has been reported to be associated with hypofibrinolysis and a deficiency in coagulation. The goal of this prospective study was to confirm or refute these findings and to establish a guide for a screening test. The coagulation systems of twenty-three patients with Legg-Calve-Perthes disease were evaluated by means of the tests which included prothrombin time, activated partial thromboplastin time, antithrombin-III (AT-III), protein C, protein S, lipoprotein(a), and anticardiolipin antibody (ACA). Study subjects were 21 males and 2 females. Mean age was 8.7 years. No abnormal results were found for Antithrombin-III and Protein S, but 2 patients had low Protein C level. Two of 23 patients had Lipoprotein(a) values greater than 30 mg/dl. Another two patients had positive finding for Anticardiolipin antibody. There were no statistical differences in all parameters between Catterall group stage in the patients with Legg-Calve-Perthes disease. We were unable to establish an association between thrombotic tendency and Legg-Calve-Perthes disease based on this prospective study. So, routine screening of patients with Legg-Calve-Perthes disease for abnormalities of antithrombotic factors would be not warranted.


Subject(s)
Female , Humans , Male , Antibodies, Anticardiolipin , Legg-Calve-Perthes Disease , Lipoprotein(a) , Mass Screening , Partial Thromboplastin Time , Prospective Studies , Protein C , Protein S , Prothrombin Time
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