1.Two cases of Sacral Agenesis
Kwang Hoe KIM ; Il Yong CHOI ; Kil Hong LIM ; Chul Soo SUNG
The Journal of the Korean Orthopaedic Association 1980;15(2):361-365
Sacral agenesis is a rare condition. This syndrome was first described by Hohl in 1852 and is usually associated with other anomalies such as vertebral deformities, deformed hypoplastic legs, urologic and gastrointestinal problems. We have experienced two cases of this deformity; one with partial sacral agenesis, and the other with partial lumbar agenesis and complete absence of sacrum.
Congenital Abnormalities
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Leg
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Sacrum
2.The Co-existence of the Gastrocnemius Tertius and Accessory Soleus Muscles.
Fatos Belgin YILDIRIM ; Levent SARIKCIOGLU ; Koh NAKAJIMA
Journal of Korean Medical Science 2011;26(10):1378-1381
A bilateral gastrocnemius tertius muscle and a unilateral accessory soleus muscle were encountered during the routine educational dissection studies. The right gastrocnemius tertius muscle consisted of one belly, but the left one of two bellies. On the left side, the superficial belly of the gastrocnemius tertius muscle had its origin from an area just above the tendon of the plantaris muscle, the deep belly from the tendon of the plantaris muscle. The accessory soleus muscle originated from the posteromedial aspect of the tibia and soleal line of the tibia and inserted to the medial surface of the calcaneus. On the right side, the gastrocnemius tertius muscle had its origin from the lateral condyle of the femur, and inserted to the medial head of the gastrocnemius muscle. The co-existence of both gastrocnemius tertius and accessory soleus muscle has not, to our knowledge, been previously reported.
*Abnormalities, Multiple
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Adult
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Humans
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Leg/*abnormalities
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Male
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Muscle, Skeletal/*abnormalities
3.Nonunion in Bilateral Ball and Socket Ankle Joint.
Journal of Korean Foot and Ankle Society 2005;9(2):231-233
Ball-and-socket deformity of the ankle joint is a rare entity that is usually associated with inequality of leg length, fibular hyperplasia, coalition of the ankle, and ray deficiency. Etiology is unknown, congenital itself or secondary to congenital conditions in the ankle. Nonunion of medial malleolar is rare in bilateral ball and socket ankle joint without lower leg deformity. We report upon this case, and include brief reviwe of the literature.
Ankle Joint*
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Ankle*
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Congenital Abnormalities
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Hyperplasia
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Leg
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Socioeconomic Factors
4.Surgical Treatment of Lipomyelomeningocele.
Sang Iel SHIM ; Sung Hak KIM ; Dong Been PARK ; Kyu Man SHIN
Journal of Korean Neurosurgical Society 1991;20(6):442-446
From January 1987 to December 1989, Six patients with lipomyelomeningocele were operated. There were 4 females and 2 males. The chief complaints that caused these patients to seek help were cosmetic effect of the mass on back, urinary incontinence, ankle deformity and weak leg. The postoperative results were as follows : Patient treated before developing neurological deficit remained unchanged neurologically. Patient treated after developing neurological deficitwere left with neurological sequelae. lipomyelomeningoceles are serious lesion which recommand early prohylactic surgery.
Ankle
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Congenital Abnormalities
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Female
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Humans
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Leg
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Male
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Urinary Incontinence
5.Extra-articular Triplane Fracuture of the Distal Tibia in Children.
Yeo Hun YUN ; Hoon JEONG ; Yi Kyoung SHIN ; Sung Gu YEO
Journal of the Korean Fracture Society 2005;18(4):459-461
PURPOSE: To demonstrate the effectiveness of the conservative treatment which was introduced to the extraarticular triplane fractures of the distal tibia. MATERIALS AND METHODS: We reviewed radiographs and medical records of eight patients with extraarticular triplane fractures of the tibia. Four patients were treated with closed reduction and internal fixation and the others with closed reduction and plaster. RESULTS: In all patients, the union of fractures was obtained. Although the physes were closed early, there was no angular deformity or leg length discrepancy. CONCLUSION: In case of extraarticular triplane fracture, except for open fracture or failure of closed reduction, conservative treatment yield good result.
Child*
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Congenital Abnormalities
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Fractures, Open
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Humans
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Leg
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Medical Records
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Tibia*
6.The Results after Surgically Managing Patients with Fibrous Dysplasia of the Proximal Femur.
Jeung Il KIM ; Jeung Tak SUH ; Kuen Tak SUH ; Hui Taek KIM ; Sang Jin CHEON ; Nam Hoon MOON
Journal of the Korean Hip Society 2009;21(3):263-271
PURPOSE: Single or multiple fibrous dysplasia of the proximal femur can cause coxa vara, Shepherd's crook deformity and a leg length discrepancy for those patients who require surgical treatment. We wanted to evaluate the efficiency of surgical treating fibrous dysplasia of the proximal femur. MATERIALS AND METHODS: Among the patients who underwent surgical treatment at our hospital during the period of June, 2001 to October, 2007, we selected 18 patients who underwent curettage and bone graft or valgus osteotomy and internal fixation due to proximal femur involvement. The clinical results were analyzed based on the patients' clinical records and radiologic findings. RESULTS: The group of patients with a normal neck-shaft angle (Group 1) could achieve satisfactory results by undergoing curettage, bone graft and internal fixation. The other group of patients who progressed to Shepherd's crook deformity (Group 2) could have satisfactory results when they underwent valgus osteotomy and soft tissue release or both proximal femur shortening osteotomy and valgus osteotomy, but not with undergoing valgus osteotomy only. CONCLUSION: Varus deformity in patients with fibrous dysplasia may progress even though they undergo valgus osteotomy. It is important to consider the preoperative biomechanical condition of the proximal femur before performing surgery.
Congenital Abnormalities
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Coxa Vara
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Curettage
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Femur
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Humans
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Leg
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Osteotomy
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Transplants
7.Variability of Radiographic Measurements of Bowleg deformity in Children: A new method for Metaphyseal Diaphyseal Angle (MDA).
Kyu Cheol NOH ; Jong Sup SHIM ; Sang Jun KIM ; Seung Jun PARK ; Ki Sun SUNG
The Journal of the Korean Orthopaedic Association 2003;38(2):179-182
PURPOSE: We investigate a new measurement method for bowleg deformity in children to reduce intra-observer and inter-observer error and to assess change in the angles measured with respect to the rotation of the lower leg. MATERIALS AND METHOD: Fifty-one children younger than 3 years old with bow leg were analyzed. To assess the intra-observer and inter-observer error of the Metaphyseal-Diaphyseal Angle, Intermetaphyseal-metaphyseal angle and Tibio-Femoral angle measurements, supine view antero-posterior radiographs of the lower legs were taken at the neutral rotation, at 10 degrees and at 20 degrees internal rotation positions. Also, the effect of the rotation of lower legs upon the measured angle was assessed by comparing and analyzing the angle values with respect to rotations of the lower leg. RESULTS: TInter-observer error showed statistically significant difference (p<0.05). All measured angles showed statistically significant differences with respect to the rotation of the lower legs. The measurement variability introduced by rotation was significantly greater than the intra-observer and inter-observer errors. The Intermetaphyseal-metaphyseal angle measurement had the lowest standard error and the highest correlation coefficient. CONCLUSION: The Intermetaphyseal-metaphyseal angle measurement seems a highly reliable method, which could be clinically utilized. Also, since the rotation of the lower legs influences the metaphyseal-diaphyseal angle, the clinician should consider this effect when studying a simple radiograph for bowleg deformity.
Child*
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Child, Preschool
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Congenital Abnormalities*
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Genu Varum
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Humans
;
Leg
8.Noncommunicating Spinal Extradural Meningeal Cyst in Thoracolumbar Spine.
Il Sup KIM ; Jae Taek HONG ; Byung Chul SON ; Sang Won LEE
Journal of Korean Neurosurgical Society 2010;48(6):534-537
Spinal extradural meningeal cyst has been rarely reported, whose etiologies are assumed to be the communication of cerebrospinal fluid (CSF) between intradural subarchnoid space and cyst due to the congenital defect in dura mater. Although the CSF communication due to this defect can be found, in most case, few cases in which there is a lack of the communication have also been reported. We report a case of the huge extradural meningeal cyst occurring in the thoracolumbar spine (from T10 to L2) where there was a lack of the communication between the intradural subarachnoid space and cyst in a 46-year-old man who presented with symptoms that were indicative of progressive paraparesis and leg pain. The patient underwent laminectomy and cyst excision. On intraoperative findings, the dura was intact and there was a lack of the communication with intradural subarachnoid space. Immediately after the surgery, weakness and leg pain disappeared shortly.
Congenital Abnormalities
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Dura Mater
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Humans
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Laminectomy
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Leg
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Middle Aged
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Paraparesis
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Spine
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Subarachnoid Space
9.Surgical Correction and Osteosynthesis for Cranial Displaced Pelvic Nonunion: Technical Note and Two Cases Report Regarding Anterior Correction and Osteosynthesis Following Posterior Release.
Kwang Cheon CHOI ; Ji Yoon HA ; Weon Yoo KIM
Journal of the Korean Fracture Society 2014;27(2):151-156
Nonunion of an unstable pelvic fracture with cranial displacement pelvic surgery is technically difficult due to a large amount of bleeding and the risk of nerve damage. In addition, surgical correction of leg length discrepancy by reduction of a dislocated sacroiliac joint is in high demand. Nevertheless, when a patient is strongly disabled by a pelvic deformity, surgical correction may be necessary. Two patients with pelvic deformity were treated successfully by surgical correction and osteosynthesis.
Congenital Abnormalities
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Fractures, Ununited
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Hemorrhage
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Humans
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Leg
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Pelvic Bones
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Sacroiliac Joint
10.A Case of Amniotic Band Syndrome: Craniofacial Deformity and Amputation of Lower Leg.
Kyu Jeong JEON ; Won Joung KIM ; Eun Hye LEE ; Yong Hee LEE ; Sung Woon JANG
Korean Journal of Obstetrics and Gynecology 2002;45(4):718-722
The amniotic band syndrome is rare congenital deformity, presumably due to rupture of amniotic sac during the early pregnancy and appears to cause fetal injury through deformation, malformation, or disruption. This syndrome is given many names yet follows a clearly defined clinical pattern. The diagnosis was based on sonographic visualization of either amniotic bands or bands associated with fetal deformation or deformities in nonembryologic distribution. Recently, we experienced a case of amniotic band syndrome, in which partial absence of cranial bone, asymmetric facial dysmorphism and amputation of right lower leg were detected. At our best knowledge, this is one of few case describing prenatal ultrasound diagnosis of amniotic band syndrome in Korea. So, we present this case with a brief review of the literatures.
Amniotic Band Syndrome*
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Amputation*
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Congenital Abnormalities*
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Diagnosis
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Infant, Newborn
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Korea
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Leg*
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Pregnancy
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Rupture
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Ultrasonography