1.Longitudinal Supraspinatus Tear Associated with Antegrade Humeral Intramedullary Nailing: A Case Report and Literature Review with Focus Placed on Nail Entry Point.
Min Soo SHON ; Tae Jung BANG ; Jae Chul YOO
Clinics in Shoulder and Elbow 2015;18(1):47-51
Iatrogenic damage of the rotator cuff followed by postoperative shoulder function loss is a potential complication after antegrade intramedullary nailing (AIN) for a humeral fracture. The authors present a case of arthroscopic rotator cuff repair and subacromial decompression of a non-healed rotator cuff tendon (mainly supraspinatus) and secondary impingement syndrome caused either by the tear or a proud nail after AIN for a mid-shaft humeral fracture. At presentation, the patient complained of right shoulder pain and 'snapping', especially during forward elevation and abduction of the shoulder, of 4 years duration. Right shoulder pain started sometime after pain due to the humeral shaft fracture, operation had subsided, and persisted after nail removal. Arthroscopic findings showed a longitudinal rotator cuff tear at the nail entry point that had not healed and severe fibrous hypertrophy on the acromion underspace, which is a unique finding since most longitudinal splits of tendon fibers are more likely to heal than conventional rotator cuff tears detached from bone. The torn rotator cuff was repaired after debridement and placing side-to-side sutures. At his 34-month follow-up after rotator cuff repair, the patient showed complete recovery and had excellent clinical scores.
Acromion
;
Arthroscopy
;
Debridement
;
Decompression
;
Follow-Up Studies
;
Fracture Fixation, Intramedullary*
;
Humans
;
Humeral Fractures
;
Hypertrophy
;
Rotator Cuff
;
Shoulder
;
Shoulder Pain
;
Sutures
;
Tendons
2.A Case of Giant Fibrous Histiocytoma.
Yoon Kee PARK ; Min Geol LEE ; Dong Sik BANG ; Tae Jung KWON ; Jung Sook KIM
Korean Journal of Dermatology 1984;22(1):83-88
Fibrous histiocytomas are characterized by a variable combination of cells with fibroblastic and histiocytic features. They exhibit a distinctive but inconstant cellular arrangement referred to as a storiform or cartwheel pattern. Considerable corfusion has enveloped these tumors as a result of their various terminology-fibrous histiocytoma, dermatofibroma, sclerosing hemangioma, fibroxanthoma, subepidermal nodular fibrosis, xanthogranuloma, giant cell tumor of tendon sheath. A histologically benign but locally infiltrating, 15 * 20cm sized, fibrous histiocytoma was found in the posterior aspect of left thigh of a 17-year-old man. The tumor was incompletely excised due to adhesion of the tumor mass to sciatic nerve and then radiation therpy was combined, Histogenesis and prognostic aspects of the tumor are discussed.
Adolescent
;
Fibroblasts
;
Fibrosis
;
Giant Cell Tumors
;
Histiocytoma
;
Histiocytoma, Benign Fibrous*
;
Humans
;
Sciatic Nerve
;
Tendons
;
Thigh
3.Amino Acid Substitution Caused by Mutated rpoB Gene of Rifampin - Resistant Mycobacterium tuberculosis.
Dong Taek CHO ; Yoo Chul LEE ; Sung Hyuk BANG ; Jung Min KIM
Journal of the Korean Society for Microbiology 1997;32(4):389-399
Mobility shifts in non-denatured gel electrophoresis of PCR-amplified Rif' region in each of fifteen different mutants of M. tuberculosis were discerned by single strand conformation polymorphism (SSCP) analysis. The findings of mobility differences between rifampin-resistant and susceptible strains showed an excellent agreement with data obtained by traditional susceptibility test. SSCP-PCR seemed to replace the cultivation method of susceptibility test that was known to be time-consuming, labor wasting, and skeptical in quality control. After screening of rpoB gene mutation by SSCP-PCR, detection of specific sequence changes in the region of rpoB gene was attempted through the procedures of PCR-amplification, cloning of PCR-products using pGEM-T vector and DNA thermocycling sequencing. Fifteen different types of mutations were identified among fifty strains of rifampin-resistant strains while five rifampin-susceptible control strains showed no sequence changes of rpoB gene as well as reference strain H37rv. Most mutation appeared to be a point mutation due to substitution or deletion except seven mutants showing somewhat complex mutation. Each of mut#ated loci inclined to clustering within a region of eighteen amino acids involving eight codons. The most common mutation of Ser425 shared among twenty-nine mutants and followed by eleven mutants of His420. Several mutants alleles identified in this study appeared to be dissimilar to those of previous reports.
Alleles
;
Amino Acid Substitution*
;
Amino Acids
;
Clone Cells
;
Cloning, Organism
;
Codon
;
DNA
;
Electrophoresis
;
Mass Screening
;
Mycobacterium tuberculosis*
;
Mycobacterium*
;
Point Mutation
;
Quality Control
;
Rifampin*
;
Tuberculosis
4.Definition, assessments, and current research on sarcopenia in children: a narrative review
Annals of Clinical Nutrition and Metabolism 2024;16(2):49-56
Purpose:
Sarcopenia is a well-established prognostic factor for the clinical outcomes of adult patients with cancer and chronic diseases and correlates with increased intensive care unit admissions and prolonged hospital stays. However, research on sarcopenia in children is limited due to its undefined criteria and a lack of studies exploring its impact on clinical outcomes.Current concept: The challenges in pediatric sarcopenia research include the absence of standardized body composition methods to quantify muscle mass and muscular function, as well as inconsistencies in definitions.Additionally, there is a lack of age- and gender-specific normative data, particularly for young children and infants. Most studies also lack assessments of muscle function, which can lead to bias and misclassification of sarcopenia. The field is further hindered by poor study quality, limited outcome-focused research, and a dearth of longitudinal data.While some studies suggest that various diseases can affect children’s lean muscle mass, few have linked changes in muscle mass to clinical outcomes.
Conclusion
The existing literature on pediatric sarcopenia and its relationship with medical and surgical outcomes is sparse and indicates poorer outcomes associated with sarcopenia. Although extensive research has established a link between sarcopenia and adverse outcomes in adults, information on its impact in pediatric populations remains scarce. Further studies are needed to elucidate the association between muscle mass and outcomes in pediatric surgical patients.
5.Percutaneous Needle Aspiration Biopsy of Chest Lesions: Effectivenese When Using an 18-Gauge Needle.
So Sun KIM ; Seong Min KIM ; Gyoo Sik JUNG ; Young Duk JOH ; Jin Do HUH ; Bang HUH
Journal of the Korean Radiological Society 1995;32(1):103-108
PURPOSE: Results of 181 percutaneous needle aspiration biopsies performed with an 18-gauge needle during a period of 3 years were analyzed to determine efficacy and safety of the procedure. MATERIALS AND METHODS: Biposies were performed in patients that could not be diagnosed by bronchoscopy or sputum cytology. The biopsy procedure with 18-gauge Crown needle was guided by fiuoroscopy. The biopsy specimen placed in 10% formalin solution were histologically confirmed. RESULTS: In 160 patients(89%), the positive diagnosis was made by percutaneous needle aspiration biopsy. There were 153 lung lesions(120 malignant and 33 benign lesions) and 7 mediastinal lesions. the diagnostic accuracy of malignant and benign disease was 91% and 80% respectively. Complications included pneumothorax(n=11) and hemothorax(n=l):six of them required treatment with chest tube and the remainder showed spontaneous resporption. CONCLUSION: PCNB with an 18-gauge needle provided a reliable, relatively safe diagnostic tool to establish the diagnosis of both malignant and benign chest lesions.
Biopsy
;
Biopsy, Needle*
;
Bronchoscopy
;
Chest Tubes
;
Crowns
;
Diagnosis
;
Formaldehyde
;
Humans
;
Lung
;
Needles*
;
Sputum
;
Thorax*
6.Percutaneous Needle Aspiration Biopsy of Chest Lesions: Effectivenese When Using an 18-Gauge Needle.
So Sun KIM ; Seong Min KIM ; Gyoo Sik JUNG ; Young Duk JOH ; Jin Do HUH ; Bang HUH
Journal of the Korean Radiological Society 1995;32(1):103-108
PURPOSE: Results of 181 percutaneous needle aspiration biopsies performed with an 18-gauge needle during a period of 3 years were analyzed to determine efficacy and safety of the procedure. MATERIALS AND METHODS: Biposies were performed in patients that could not be diagnosed by bronchoscopy or sputum cytology. The biopsy procedure with 18-gauge Crown needle was guided by fiuoroscopy. The biopsy specimen placed in 10% formalin solution were histologically confirmed. RESULTS: In 160 patients(89%), the positive diagnosis was made by percutaneous needle aspiration biopsy. There were 153 lung lesions(120 malignant and 33 benign lesions) and 7 mediastinal lesions. the diagnostic accuracy of malignant and benign disease was 91% and 80% respectively. Complications included pneumothorax(n=11) and hemothorax(n=l):six of them required treatment with chest tube and the remainder showed spontaneous resporption. CONCLUSION: PCNB with an 18-gauge needle provided a reliable, relatively safe diagnostic tool to establish the diagnosis of both malignant and benign chest lesions.
Biopsy
;
Biopsy, Needle*
;
Bronchoscopy
;
Chest Tubes
;
Crowns
;
Diagnosis
;
Formaldehyde
;
Humans
;
Lung
;
Needles*
;
Sputum
;
Thorax*
7.Longitudinal Supraspinatus Tear Associated with Antegrade Humeral Intramedullary Nailing: A Case Report and Literature Review with Focus Placed on Nail Entry Point
Min Soo SHON ; Tae Jung BANG ; Jae Chul YOO
Journal of the Korean Shoulder and Elbow Society 2015;18(1):47-51
Iatrogenic damage of the rotator cuff followed by postoperative shoulder function loss is a potential complication after antegrade intramedullary nailing (AIN) for a humeral fracture. The authors present a case of arthroscopic rotator cuff repair and subacromial decompression of a non-healed rotator cuff tendon (mainly supraspinatus) and secondary impingement syndrome caused either by the tear or a proud nail after AIN for a mid-shaft humeral fracture. At presentation, the patient complained of right shoulder pain and 'snapping', especially during forward elevation and abduction of the shoulder, of 4 years duration. Right shoulder pain started sometime after pain due to the humeral shaft fracture, operation had subsided, and persisted after nail removal. Arthroscopic findings showed a longitudinal rotator cuff tear at the nail entry point that had not healed and severe fibrous hypertrophy on the acromion underspace, which is a unique finding since most longitudinal splits of tendon fibers are more likely to heal than conventional rotator cuff tears detached from bone. The torn rotator cuff was repaired after debridement and placing side-to-side sutures. At his 34-month follow-up after rotator cuff repair, the patient showed complete recovery and had excellent clinical scores.
Acromion
;
Arthroscopy
;
Debridement
;
Decompression
;
Follow-Up Studies
;
Fracture Fixation, Intramedullary
;
Humans
;
Humeral Fractures
;
Hypertrophy
;
Rotator Cuff
;
Shoulder
;
Shoulder Pain
;
Sutures
;
Tendons
8.A Case of Multiple Trichoepitheliomas and Basal Cell Carcinomas Co-existed on the Nose
Hyo Jung KIM ; Ju Hee HAN ; Chul Hwan BANG ; Jun Young LEE ; Ji Hyun LEE ; Young Min PARK
Korean Journal of Dermatology 2019;57(3):164-166
No abstract available.
Carcinoma, Basal Cell
;
Nose
9.The Relationship between PTEN Tumor Suppressor Gene and Vascular Endothelial Growth Factor-Mediated Angiogenesis in Breast Cancer.
Jean Kyung PARK ; Min Jung JUNG ; Bong Kwon CHUN ; Bang HUR
Korean Journal of Pathology 2004;38(2):100-105
BACKGROUND: PTEN is a novel tumor suppressor gene located at chromosome 10q23.3. Loss of PTEN function has been implicated in the progression of several types of cancer. Angiogenesis is a critical factor in tumor growth and metastasis. We investigated PTEN expression in invasive breast cancers and described its role in the regulation of angiogenesis related to vascular endothelial growth factor (VEGF). METHODS: Forty-five, surgically resected, formalin-fixed and paraffin embedded breast cancer tissue samples were analyzed for PTEN and VEGF expressions by immunohistochemistry and for microvessel density (MVD) by CD34 immunostaining. RESULTS: Loss of PTEN expression was found in 35.6% (16/45) of the breast cancer tissues, all of which showed positive VEGF expression. Among 29 cases with normal PTEN expression, 15 (51.7%) were VEGF positive. MVD was significantly higher in tumors with a loss of PTEN expression than in those with normal PTEN expression. CONCLUSION: A loss of PTEN expression might increase the VEGF-related angiogenesis in breast cancer. There was no correlation between PTEN expression and clinicopathologic parameters. Detection of the loss of PTEN expression may serve as a useful biologic marker for progression in invasive breast cancer.
Biomarkers
;
Breast Neoplasms*
;
Breast*
;
Genes, Tumor Suppressor*
;
Immunohistochemistry
;
Microvessels
;
Neoplasm Metastasis
;
Paraffin
;
Vascular Endothelial Growth Factor A
10.Understanding Epistatic Interactions between Genes Targeted by Non-coding Regulatory Elements in Complex Diseases.
Min Kyung SUNG ; Hyoeun BANG ; Jung Kyoon CHOI
Genomics & Informatics 2014;12(4):181-186
Genome-wide association studies have proven the highly polygenic architecture of complex diseases or traits; therefore, single-locus-based methods are usually unable to detect all involved loci, especially when individual loci exert small effects. Moreover, the majority of associated single-nucleotide polymorphisms resides in non-coding regions, making it difficult to understand their phenotypic contribution. In this work, we studied epistatic interactions associated with three common diseases using Korea Association Resource (KARE) data: type 2 diabetes mellitus (DM), hypertension (HT), and coronary artery disease (CAD). We showed that epistatic single-nucleotide polymorphisms (SNPs) were enriched in enhancers, as well as in DNase I footprints (the Encyclopedia of DNA Elements [ENCODE] Project Consortium 2012), which suggested that the disruption of the regulatory regions where transcription factors bind may be involved in the disease mechanism. Accordingly, to identify the genes affected by the SNPs, we employed whole-genome multiple-cell-type enhancer data which discovered using DNase I profiles and Cap Analysis Gene Expression (CAGE). Assigned genes were significantly enriched in known disease associated gene sets, which were explored based on the literature, suggesting that this approach is useful for detecting relevant affected genes. In our knowledge-based epistatic network, the three diseases share many associated genes and are also closely related with each other through many epistatic interactions. These findings elucidate the genetic basis of the close relationship between DM, HT, and CAD.
Coronary Artery Disease
;
Deoxyribonuclease I
;
Diabetes Mellitus
;
Diabetes Mellitus, Type 2
;
DNA
;
Gene Expression
;
Genome-Wide Association Study
;
Hypertension
;
Korea
;
Polymorphism, Single Nucleotide
;
Regulatory Sequences, Nucleic Acid
;
Transcription Factors