1.The Usefulness of Postoperative Pinhole Bone Scintigraphy in the Assessment of Prognosis after Multiple Drilling or Vascularized Bone Graft in Patients with Avascular Necrosis of Femoral Head.
Yong An CHUNG ; Sung Hoon KIM ; Kyung Ah CHUN ; Young Ha PARK ; Hyeong Seon SOHN ; Soo Kyo CHUNG ; Mun Kab SONG
Korean Journal of Nuclear Medicine 1999;33(4):405-412
PURPOSE:It is important to evaluate the healing process of avascular necrosis (AVN) involving femoral head after treatment. The purpose of this study was to assess the usefulness of pinhole bone scintigraphy in the AVN of femoral head after surgery. MATERIALS AND METHODS: We analyzed the changing pattern of pinhole bone scintigram in 21 femoral heads of 16 patients (14 lesions/11 male, 7 lesions/5 female, mean age: 39.4 yrs) before and after multiple drilling or vascularized bone grafting for AVN of the femoral head. In all patients, pre-operative scintigrams were obtained at 1 to 3 months before treatment and the first post-operative scintigrams were obtained at 1 to 3 months after treatment. All patients were followed for 2 to 4 years after operation. RESULTS: The findings of the pinhole scintigrams were divided into three patterns: 1) curvilinear, 2) scattered spotty and 3) undetermined. The 10 of 11 lesions with curvilinear pattern had good postoperative clinical and radiological follow-up findings. However, all 6 lesions with scattered spotty pattern showed poor postoperative findings, which necessitated total hip joint replacement. Of the 4 lesions with undetermined pattern, 2 required total hip joint replacement. There was significant difference in postoperative prognosis between the curvilinear and scattered spotty patterns (p<0.05). CONCLUSION: We conclude that the pattern of pinhole bone scintigram obtained within 1 to 3 months after multiple drilling or vascularized bone graft operation is a useful prognostic indicator in the AVN of femoral head.
Bone Transplantation
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Female
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Follow-Up Studies
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Head*
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Hip Joint
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Humans
;
Male
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Necrosis*
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Prognosis*
;
Radionuclide Imaging*
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Technetium Tc 99m Medronate
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Transplants*
2.Bone scintigraphic findings in leukemic patients.
Hyo Sun CHOI ; Jeong Mi PARK ; Hyeong Seon SOHN ; Soo Kyo CHUNG ; Choon Yul KIM ; Yong Whee BAHK ; Kyung Sub SHINN
Korean Journal of Nuclear Medicine 1992;26(1):101-105
No abstract available.
Humans
3.Bile Duct Cannulation Guided by a Percutaneous Transhepatic Biliary Drainage (PTBD) Tube: Modified Rendezvous Procedure.
Hong Joo KIM ; Seon Hyeong CHOI ; Jung Ho PARK ; Dong Il PARK ; Yong Kyun CHO ; Chong Il SOHN ; Woo Kyu JEON ; Byung Ik KIM
Korean Journal of Gastrointestinal Endoscopy 2007;34(3):138-142
BACKGROUND/AIMS: To describe a simple and useful modification of the rendezvous technique using a PTBD tube as guidance. METHODS: From January 2005 to August 2006, a total of 436 ERCPs were performed. A diagnosis of choledocholithiasis was made in 235 cases. Deep cannulation of the bile duct using standard techniques was unsuccessful in 27 patients (11.5%). A precut papillotomy led to successful cannulation in 16 out of these 27 patients (59.3%). The remaining 11 patients (40.7%) underwent PTBD with the tube tip placed in the second portion of the duodenum. Bile duct cannulation was attempted with the guidance of a PTBD tube in 9 cases. In the other 2 cases, the transduodenal approach was impossible due to a previous Billroth II operation. RESULTS: Bile duct cannulation guided by a PTBD tube, which is also known as a modified rendezvous procedure, was successful in 9 out of 11 patients (81.8%). Deep cannulation of the bile duct was achieved in 100% of patients, who could be treated by endoscopy. There were 7 cases of transient hyperamylasemia (77.8%) but no procedure-related major complications or mortality. CONCLUSIONS: Bile duct cannulation guided by a PTBD tube in patients with choledocholithiasis can be recommended when ERCP is unsuccessful using the standard technique.
Bile Ducts*
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Bile*
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Catheterization*
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Cholangiopancreatography, Endoscopic Retrograde
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Choledocholithiasis
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Diagnosis
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Drainage*
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Duodenum
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Endoscopy
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Gastroenterostomy
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Humans
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Hyperamylasemia
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Mortality
4.Activated Leukocyte Cell Adhesion Molecule Modulates Th2 Immune Response in Atopic Dermatitis
Mi Seon OH ; Jung Yeon HONG ; Mi Na KIM ; Eun Ji KWAK ; Soo Yeon KIM ; Eun Gyul KIM ; Kyung Eun LEE ; Yun Seon KIM ; Hye Mi JEE ; Seo Hyeong KIM ; In Suk SOL ; Chang Ook PARK ; Kyung Won KIM ; Myung Hyun SOHN
Allergy, Asthma & Immunology Research 2019;11(5):677-690
PURPOSE: Activated leukocyte cell adhesion molecule (ALCAM), a member of the immunoglobulin superfamily, is highly expressed on dendritic cells. ALCAM and its receptor CD6 are co-stimulatory molecules in the immunological synapse; their interaction is required for T cell activation. While atopic dermatitis (AD) is recognized as a T helper 2 (Th2)-mediated allergic disease, the role of ALCAM in its pathogenesis is unclear. METHODS: ALCAM levels were measured in the serum of AD patients and AD-induced murine model by ovalbumin treatment. We next investigated transepidermal water loss, clinical score, Th2-immune responses, skin barrier gene expression and T-cell activation using wild-type (WT) and ALCAM deficiency mice. An oxazolone-induced AD-like model was also established and analyzed using WT- and ALCAM-deficient mice. RESULTS: We found that serum ALCAM levels were elevated in pediatric AD patients as well as WT AD mice, whereas Th2-type cytokine production and AD symptoms were suppressed in ALCAM-deficient mice. In addition, CD4+ effector T-cell counts in murine skin and skin-draining lymph nodes were lower in ALCAM-deficient mice than in their WT counterparts. ALCAM deficiency was also linked to higher expression of skin barrier genes and number of lamellar bodies. CONCLUSIONS: These findings indicate that ALCAM may contribute to AD pathogenesis by meditating a Th2-dominant immune response and disrupting the barrier function of the skin.
Activated-Leukocyte Cell Adhesion Molecule
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Animals
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Dendritic Cells
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Dermatitis, Atopic
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Gene Expression
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Humans
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Immunoglobulins
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Immunological Synapses
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Lymph Nodes
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Mice
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Ovalbumin
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Skin
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T-Lymphocytes
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Water