1.Pathogenesis of Transplant Glomerulopathy.
Beom Jin LIM ; Hyeon Joo JEONG
The Journal of the Korean Society for Transplantation 2011;25(2):71-75
Transplant glomerulopathy is a late complication of renal transplantation. The characteristic morphology of transplant glomerulopathy includes thickening of glomerular capillary loops with double contour, and duplication of glomerular basement membrane on electron microscopy. Clinical and experimental evidences support the role of antibody-mediated immune mechanism in the development of transplant glomerulopathy. Antibody-induced endothelial cell injury is the key pathogenesis of transplant glomerulopathy. The evolution of transplant glomerulopathy in the context of immunologic injury is briefly reviewed.
Capillaries
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Endothelial Cells
;
Glomerular Basement Membrane
;
Graft Rejection
;
Immunity, Humoral
;
Kidney Glomerulus
;
Kidney Transplantation
;
Microscopy, Electron
;
Transplants
4.Overview of IgG4-Related Tubulointerstitial Nephritis and Its Mimickers.
Hyeon Joo JEONG ; Su Jin SHIN ; Beom Jin LIM
Journal of Pathology and Translational Medicine 2016;50(1):26-36
Tubulointerstitial nephritis (TIN) is the most common form of renal involvement in IgG4-related disease. It is characterized by a dominant infiltrate of IgG4-positive plasma cells in the interstitium and storiform fibrosis. Demonstration of IgG4-positive plasma cells is essential for diagnosis, but the number of IgG4-positive cells and the ratio of IgG4-positive/IgG-positive plasma cells may vary from case to case and depending on the methods of tissue sampling even in the same case. IgG4-positive plasma cells can be seen in TIN associated with systemic lupus erythematosus, Sjogren syndrome, or anti-neutrophil cytoplasmic antibody-associated vasculitis, which further add diagnostic confusion and difficulties. To have a more clear view of IgG4-TIN and to delineate differential points from other TIN with IgG4-positive plasma cell infiltrates, clinical and histological features of IgG4-TIN and its mimickers were reviewed. In the rear part, cases suggesting overlap of IgG4-TIN and its mimickers and glomerulonephritis associated with IgG4-TIN were briefly described.
Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
;
Diagnosis
;
Fibrosis
;
Glomerulonephritis
;
Glomerulonephritis, Membranous
;
Lupus Erythematosus, Systemic
;
Lupus Nephritis
;
Nephritis, Interstitial*
;
Plasma Cells
;
Sjogren's Syndrome
;
Tin
5.A Case of Giant Tonsillolith.
Oh Jin KWON ; Jong Beom LIM ; Jin Pyeong KIM ; Seung Hoon WOO
Korean Journal of Otolaryngology - Head and Neck Surgery 2011;54(7):486-488
The tonsillolith is a white or yellow colored calcified lesion that forms in the crypts of the palatine tonsil. Small tonsilloliths are frequently found on tonsils, while giant tonsilloliths are a rare clinical entity. We had a 35-years old female patient, who presented throat discomfort due to a giant tonsillolith. The stone was removed and tonsillectomy was performed. We reviewed the literature on this rare clinical entity.
Female
;
Humans
;
Palatine Tonsil
;
Pharynx
;
Tonsillectomy
6.Pathology of C3 Glomerulopathy
Su Jin SHIN ; Yoonje SEONG ; Beom Jin LIM
Childhood Kidney Diseases 2019;23(2):93-99
C3 glomerulopathy is a renal disorder involving dysregulation of alternative pathway complement activation. In most instances, a membranoproliferative pattern of glomerular injury with a prevalence of C3 deposition is observed by immunofluorescence microscopy. Dense deposit disease (DDD) and C3 glomerulonephritis (C3GN) are subclasses of C3 glomerulopathy that are distinguishable by electron microscopy. Highly electron-dense transformation of glomerular basement membrane is characteristic of DDD. C3GN should be differentiated from post-infectious glomerulonephritis and other immune complex-mediated glomerulonephritides showing C3 deposits.
Complement Activation
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Complement Pathway, Alternative
;
Dichlorodiphenyldichloroethane
;
Glomerular Basement Membrane
;
Glomerulonephritis
;
Glomerulonephritis, Membranoproliferative
;
Microscopy, Electron
;
Microscopy, Fluorescence
;
Pathology
;
Prevalence
7.Rhabdoid Cholangiocarcinoma: A Variant of Cholangiocarcinoma with Aggressive Behavior.
Beom Jin LIM ; Kyung Sik KIM ; Joon Seok LIM ; Myeong Jin KIM ; Chanil PARK ; Young Nyun PARK
Yonsei Medical Journal 2004;45(3):543-546
A rhabdoid cholangiocarcinoma is a very rare variant of sarcomatous cholangiocarcinomas. Here, we report a vimentin positive cholangiocarcinoma showing rhabdoid features in the entire tumor, with a very aggressive behavior. A 41-year-old woman was admitted to our hospital due to a huge hepatic mass. The resected liver revealed a 17x15cm sized solid mass with extensive necrosis and an infiltrative border. On microscopic examination, the entire tumor was composed of loosely cohesive round to polygonal cells, with rhabdoid features having abundant eosinophilic glassy cytoplasm and eccentrically located vesicular nuclei. Some tumor cells contained intracytoplasmic mucin vacuoles, but definite areas of glandular differentiation or spindle cell were not found. Immunohistochemical staining showed a diffuse strong positive reaction to pan-cytokeratin and vimentin, and focal positivity for the carcinoembryonic antigen. Other immunohistochemical stainings for cytokeratin 7, cytokeratin 20, S-100 protein, HMB-45, desmin, alpha-smooth muscle actin, c-kit, CD34, alpha-fetoprotein, anti-hepatocyte antigen, chromogranin and synaptophysin were all negative. After two months, the patient developed a local recurrence along the resection margin, and multiple hematogenous metastases to the lung and liver were seen on the follow-up CT scan.
Adult
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Cholangiocarcinoma/chemistry/*pathology
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Female
;
Human
;
Liver Neoplasms/chemistry/*pathology
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Magnetic Resonance Imaging
;
Prognosis
;
Rhabdoid Tumor/chemistry/*pathology
;
Support, Non-U.S. Gov't
;
Tomography, X-Ray Computed
;
Vimentin/analysis
8.Diagnosis and Treatment for the Extraforaminal Lumbar Disc Herniation.
Han CHANG ; Jong Beom PARK ; In Joo LEE ; Seung Key KIM ; Sung Jin PARK ; Woo Sung CHOI ; Seung Jae LIM
Journal of Korean Society of Spine Surgery 1998;5(1):102-108
STUDY DESIGN: We retrospectively reviewed nine patients of lumbar extraforaminal disc herniation which underwent conservative or surgical treatment. OBJECTIVES: We evaluated the clinical characteristics, accuracy of diagnostic methods, and result of conservative or surgical treatment for the lumbar extraforaminal disc herniation. SUMMARY OF BACKGROUND DATA: Lumbar extraforaminal disc herniation represents an important component of lumbar disc herniation because of the difficulty in diagnosis and the difference in clinical characteristics and surgical approaches in contrast to usual intracanalicular disc herniation. MATERIALS AND METHODS: Nine patients which we have experienced from March 1994 to February 1997 were evaluated by physical examination, magnetic resonance imaging, EMG, and disco-enhanced computed tomogram. There were 4 males and 5 females, and average age was 42.4 years. RESULTS: The level of herniation was 4 cases at L4-5 and 5 at L5-S1. Radiating pain was chief complaint but low back pain was absent or mild. Accuracy of disco-enhanced computed tomogram was superior to that of magnetic resonance imaging. The results of conservative treatment were good in 2 cases(40%), fair in 2 cases(40%), and poor in 1 case(20%). And those of surgical treatment including partial laminectomy, medial facetectomy, and discectomy or extraforaminal approach were excellent in 3 cases(75%), good in 1 case(25%) according to the grading of MacNab. CONCLUSIONS: Lumbar extraforaminal disc herniation represents compressive symptoms of upper lumbar root of the involved level characteristically. Location and degree of disc herniation is an important tractor for determining the surgical approach, and disco-enhanced computed tomogram is a definite diagnostic method.
Diagnosis*
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Diskectomy
;
Female
;
Humans
;
Laminectomy
;
Low Back Pain
;
Magnetic Resonance Imaging
;
Male
;
Physical Examination
;
Retrospective Studies
9.Pathogenesis of Focal Segmental Glomerulosclerosis.
Beom Jin LIM ; Jae Won YANG ; Woo Sung DO ; Agnes B FOGO
Journal of Pathology and Translational Medicine 2016;50(6):405-410
Focal segmental glomerulosclerosis (FSGS) is characterized by focal and segmental obliteration of glomerular capillary tufts with increased matrix. FSGS is classified as collapsing, tip, cellular, perihilar and not otherwise specified variants according to the location and character of the sclerotic lesion. Primary or idiopathic FSGS is considered to be related to podocyte injury, and the pathogenesis of podocyte injury has been actively investigated. Several circulating factors affecting podocyte permeability barrier have been proposed, but not proven to cause FSGS. FSGS may also be caused by genetic alterations. These genes are mainly those regulating slit diaphragm structure, actin cytoskeleton of podocytes, and foot process structure. The mode of inheritance and age of onset are different according to the gene involved. Recently, the role of parietal epithelial cells (PECs) has been highlighted. Podocytes and PECs have common mesenchymal progenitors, therefore, PECs could be a source of podocyte repopulation after podocyte injury. Activated PECs migrate along adhesion to the glomerular tuft and may also contribute to the progression of sclerosis. Markers of activated PECs, including CD44, could be used to distinguish FSGS from minimal change disease. The pathogenesis of FSGS is very complex; however, understanding basic mechanisms of podocyte injury is important not only for basic research, but also for daily diagnostic pathology practice.
Actin Cytoskeleton
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Age of Onset
;
Capillaries
;
Diaphragm
;
Epithelial Cells
;
Foot
;
Glomerulosclerosis, Focal Segmental*
;
Nephrosis, Lipoid
;
Pathology
;
Permeability
;
Podocytes
;
Rabeprazole
;
Sclerosis
;
Wills
10.Anterior and Posterior Corneal Spherical Aberration Measured With Pentacam in the Korean.
Tae Hyung LIM ; Jong Rak LEE ; Kee Yong CHOI ; Beom Jin CHO
Journal of the Korean Ophthalmological Society 2010;51(6):816-821
PURPOSE: To evaluate the spherical aberrations of the anterior and posterior surfaces of normal corneas using Pentacam in a Korean sample population and determine their ranges and changes with age. METHODS: We used Pentacam (Oculus Inc.,Germany) to measure the anterior and posterior corneal spherical aberrations of 240 eyes in 240 patients with normal corneas who visited our clinic. The means and ranges of spherical aberrations and their changes with age were determined. We examined both eyes of 90 patients to confirm the inter-ocular symmetry in spherical aberration. RESULTS: The mean age of the 240 patients (M:F=103:137) was 49.8 years (range: 20-79), and the mean spherical aberrations of the anterior and posterior surfaces of the cornea were 0.230+/-0.078 micrometer, and -0.04+/-0.021 micrometer, respectively. The mean total corneal spherical aberration was 0.19+/-0.087 micrometer. There were no differences between males and females, and inter-ocular symmetry was observed in all tested patients. There was a tendency for the values of anterior, posterior and total corneal spherical aberration to increase with age. Ranges of spherical aberrations were from -0.177 micrometer to 0.423 micrometer in the anterior cornea, from -0.083 micrometer to 0.034 micrometer in the posterior cornea, and from -0.238 micrometer to 0.410 micrometer in the total cornea. CONCLUSIONS: In a Korean population, the mean total corneal spherical aberration was 0.19 micrometer, which was shown to increase with age. Some patients were shown to have an extreme value. Based on these results, a preoperative analysis for corneal spherical aberration may be helpful when selecting aspheric intraocular lenses.
Cataract
;
Cornea
;
Eye
;
Female
;
Humans
;
Lenses, Intraocular
;
Male