1.Two Cases Reports of Infantile Cortical Hyperostosis
Hyung Seok KIM ; Ki Sung HONG ; Ki Do HONG
The Journal of the Korean Orthopaedic Association 1981;16(4):951-954
The infantile cortical hyperostosis is relatively rare unknown cause disease. After the first report of a case of this was that of caffey in 1945, this disease is increasing in frequency. This disease characterized by subperiosteal new bone formation on various bone, leukocytosis, increased Erythrocyte Seidmentation Rate, fever. We experienced two cases of this and reported them in this paper with a brief review of tbe literature.
Erythrocytes
;
Fever
;
Hyperostosis, Cortical, Congenital
;
Leukocytosis
;
Osteogenesis
2.Sciatic Nerve Injury in Total Hip Arthroplasty
Sung Kwan HWANG ; Ki Hong PARK
The Journal of the Korean Orthopaedic Association 1996;31(1):67-71
PURPOSE: The study of the causative factors, surgical approachs and the clinical course of symptoms related to sciatic nerve injury after THR. MATERIAL AND METHODS: A retrospective review of 6 patients with sciatic nerve injury in 669 hips total hip arthroplasty during the period from Jan., 1986 to Dec., 1994. Each patient's record was reviewed with respect to age, sex, possible etiology, clinical course, surgical approach, treatment, and clinical condition at follow-up examination. RESULTS: ➀ The increased prevalence of nerve palsy was seen in revision surgeries(4 cases, 3.2%) compared to primary arthroplasty(2 cases, 0.4%) ➁ There was 2 cases(0.8%) of sciatic nerve injury in direct lateral approach and posterior approach, 4 cases(1%) ➂ Possible mechanisms of nerve injury included excessive soft tissue traction(3 cases), electrical thermal injury(1 case), Trochanteric fracture during femoral stem removal(1 case), and overlengthening of femur(1 case). ➃ The isolated peroneal division of the sciatic nerve was injured in 5 cases, and the both peroneal and tibial divisions were injured in one case. ➄ At a following period of 5 month, recovery of neurologic function was complete in con case, and two years follow up, 4 cases had a enough recovery of neurologic function(modified Sunderland scale 1,2). However, remained one case had a persistent severe weakness & dysesthesia at even 3 years follow-up. The prognosis for neurological recovery was related the degrees to which the nerve was damaged.
Arthroplasty, Replacement, Hip
;
Femur
;
Follow-Up Studies
;
Hip
;
Humans
;
Paralysis
;
Paresthesia
;
Prevalence
;
Prognosis
;
Retrospective Studies
;
Sciatic Nerve
3.Clinical observations of hepatic encephalopathy.
Sung In HONG ; Ki Pyo HONG ; Sang Hwa LEE
Journal of the Korean Academy of Family Medicine 1991;12(8):58-64
No abstract available.
Hepatic Encephalopathy*
4.MRI features of right atrial angiosarcoma: a case report.
In Soo HONG ; Joong Wha PARK ; Ki Joon SUNG
Journal of the Korean Radiological Society 1992;28(6):854-857
Primary tumors of the heart are rare, and one-third of them are malignant. The most common malignant intracardiac tumor is angiosarcoma, which usually involves right atrium. MR features in one patients with right atrial angiosarcoma is presented and the literature briefly reviewed. Angiosarcoma demonstrated slightly heterogeneous intermediate signal intensity on T1-weighted images, high signal intensity on T2-weighted images and higher signal intensity on Gd-DTPA enhanced images. MRI provided more information regarding the extent of the tumor than 2D echocardiography or CT.
Echocardiography
;
Gadolinium DTPA
;
Heart
;
Heart Atria
;
Hemangiosarcoma*
;
Humans
;
Magnetic Resonance Imaging*
5.A Case of Gougerot-Blum Syndrome with Leukemia.
Ki Bum MYUNG ; Hong Jin KIM ; Sung Nack LEE
Korean Journal of Dermatology 1977;15(4):499-503
Gougerost-Blum syndrome is a rare disease and characterized by lichenoid papules in association with purpuric lesions. So far as we know there has been no report of, in literatures, Gougerot-Blum syndrome with leukemia. We experienced a case of typical Gougerrot_Blum syndrome with acute myeloblastic leukemia in a 30 year-old female patient. This patient complained of rashes on whole body for 2 months, and frequent epistaxis and gum bleeding for 20 days. The skin revealed miliary to rice sized rusty colored lichenoid papules on whole body especially on legs and arms. Histopathologically the skin showed the picture of Gougerot-Blum syndrome. On peripheral blood examination and bone marrow aspiration myeloblastic leukemia was confirmed. The patient was treated with 6-mercaptopurine, cytoxan and prednisolone with slight improvement of skin lesions, but no improvement of leukumia itselt.
6-Mercaptopurine
;
Adult
;
Arm
;
Bone Marrow
;
Cyclophosphamide
;
Epistaxis
;
Exanthema
;
Female
;
Gingiva
;
Granulocyte Precursor Cells
;
Hemorrhage
;
Humans
;
Leg
;
Leukemia*
;
Leukemia, Myeloid, Acute
;
Prednisolone
;
Rare Diseases
;
Skin
6.Surgical thyroid diseases.
Chang Ki HONG ; Sung Kyu LEE ; Man Soo RO
Journal of the Korean Surgical Society 1991;40(2):137-145
No abstract available.
Thyroid Diseases*
;
Thyroid Gland*
7.Osteoblastoma: A Case Report
Han Koo LEE ; Chung Yong HONG ; Sung Ki KIM
The Journal of the Korean Orthopaedic Association 1979;14(1):129-132
Osteoblastoma is a benign lesion somewhat similar to ostoid osteoma histologically but different from it clinically, roentgenologically and grossly. The autors have experienced a case of benign osteoblastoma of the neural arch of the Iumbar spine, and treated the case by total laminectomy and conflrmed with biopsy.
Biopsy
;
Laminectomy
;
Osteoblastoma
;
Osteoma
;
Spine
8.A Clinical Study on the Trochanteric Fracture of Adult
Kyu Young PARK ; Hyung Seok KIM ; Ki Sung HONG
The Journal of the Korean Orthopaedic Association 1980;15(3):487-496
Complications after surgical treatment of trochanteric fracture such as varus deformity or delayed union are frequent and there are many difficulties to maintain the stability of fragments because of the cortical deficit or comminution on medial aspect of the neck and posterior trochanteric fragment. Evans, Dimon, Sarmiento and others suggested several methods of internal fixation, furthermore it is attempted recently to reduce the fragments anatomically with sliding compression hip screw and plate. 31 cases of interal fixation on trochanteric fracture were carried out from March, 1972 to February 1979 at the Orthopaedic Department of Seoul Adventist Hospital and their comparable results were as follows. 1. Acceptable placement of metals was noted 2 cases of 6 cases in Smith-Petersen nail with Thornton plate fixation, 2 cases out of 8 cases in Smith-Petersen nail with McLaughlin plate fixation and 9 cases out of 14 cases in sliding compression hip screw and plate fixation. 2. Complications after internal fixation such as varus deformity and delayed union were noted 1 case out of 3 cases in multiple pinning, 3 cases out of 6 cases in Smith-Petersen nail with Thornton plate fixation, 4 cases out of 8 cases in Smith-Petersen nail with McLaughlin plate fixation, 4 cases out of 14 cases in sliding compression hip screw and plate fixation. 3. Required weeks in union were 18 weeks in Multiple pinning, 20 weeks in Smith-Petersen nail with Thornton plate fixation, 25 weeks in Smith-Petersen nail with McLaughlin plate fixation and 16 weeks in sliding compression hip screw and plate fixation. 4. There are few complications in treatment of trochanteric fracture with surgical procedure using Sliding compression hip screw and plate.
Adult
;
Clinical Study
;
Congenital Abnormalities
;
Femur
;
Hip
;
Humans
;
Metals
;
Neck
;
Seoul
9.Brodie's Abscess: A Case Report
Hyung Seok KIM ; Ki Sung HONG ; Sang Hoon GIL
The Journal of the Korean Orthopaedic Association 1982;17(6):1233-1236
Brodie's abscess is a primary subacute pyogenic osteomyelitis that has a thin wall of fibrous tissue and sclerotic bone. The authors have encountered a case of a Brodie's abscess that was developed in the same place of both tibia at the same time and treated the case with surgery and continuous closed irrigation.
Abscess
;
Osteomyelitis
;
Tibia
10.Symptomatic Sacroiliitis in Female Systemic Lupus Erythematosus.
Ki Do PARK ; Young Hun HONG ; Sung Dong KIM ; Dong Hwan RYU ; Coong Ki LEE
Yeungnam University Journal of Medicine 2000;17(2):161-164
We report a case of 17-year-old female with juvenile onset systemic lupus erythematosus Who developed symptomatic unilateral sacroiliitis. She had neither HLA-DR3 nir B27 antigens. Though sacroiliitis have been reported in mail SLE patient. it has been rarely reported in female patients. The rare coexistence of SLE and sacroiliitis. described in this case. may not be determined soley by genetic factors; sacroiliitis may be just an infrequent manifestation of SLE.
Adolescent
;
Female*
;
HLA-DR3 Antigen
;
Humans
;
Lupus Erythematosus, Systemic*
;
Postal Service
;
Sacroiliitis*