3.Expression of TGF-β, PDGF, Type I and II Collagen, and Osteonectin During Fracture Healing in Rat
Chi Hong KIM ; Bum Woo YEOM ; Han Kyeom KIM ; Jung Suk MOON ; Hye Rim PARK
The Journal of the Korean Orthopaedic Association 1996;31(5):1205-1217
To define the basic sequential events of the healing process in normal fracture and evaluate the role of growth regulatory molecules and extracellular matrix components, the expression of transforming growth factor β(TGF-β), platelet-derived growth factor(PDGF), type I and II collagen, and chemistry during the healing process of an experimental fracture of tibia in 41 adult rats for 7 weeks using ABC methods. The phases of inflammation, reparation, and remodeling followed each other in sequence. The inflammatory phase was characterized by hemorrhage, edema, and infiltration of inflammatory cells on the first day. During the reparative phase, the undifferentiated mesenchyme undergoes rapid chondrogenesis, followed by endochondral ossification and supplemented by appositional bone formation. At day 3, the expression of TGF-β and PDGF was noted in the undifferentiated mesenchymal cells and from day 5, these two growth factors were detected in the osteoblasts and extracellular matrix in areas of endochondral ossification and newly formed periosteal bone. From day 3, the expression of type I collagen and osteonectin was noted in the osteoblasts and extracellular matrix in both endochondral ossification and appositional bone growth as a marker of ossification. From day 3, type III collagen was mainly expressed in the plump mesenchymal cells showing chondroid differentiation and chondroid matrix as a marker of cartilaginous reparative phase. From day 14, these growth factors and extracellular matrix components were decreased in staining intensity and at the 5th week, the histology and immunostaining pattern were similar to the mature bone.
Adult
;
Animals
;
Bone Development
;
Chemistry
;
Chondrogenesis
;
Collagen Type I
;
Collagen Type III
;
Collagen
;
Edema
;
Extracellular Matrix
;
Fracture Healing
;
Hemorrhage
;
Humans
;
Inflammation
;
Intercellular Signaling Peptides and Proteins
;
Mesoderm
;
Osteoblasts
;
Osteogenesis
;
Osteonectin
;
Rats
;
Tibia
;
Transforming Growth Factors
4.Childhood Granulomatous Periorificial Dermatitis of 2 Years Duration Treated by Tetracycline.
Bo Young KIM ; Sook In RYU ; Ji Hyun PARK ; Hye Rim MOON ; Il Hwan KIM
Korean Journal of Dermatology 2018;56(8):508-510
No abstract available.
Dermatitis*
;
Tacrolimus
;
Tetracycline*
5.Atypical Proliferative Nodule with Melanocytic Intraepidermal Pagetoid Spreading Arising within a Congenital Melanocytic Nevus in a Pregnant Woman.
Hye Rim MOON ; Mi Hye LEE ; Chong Hyun WON ; Sung Eun CHANG ; Mi Woo LEE ; Jee Ho CHOI ; Kee Chan MOON
Annals of Dermatology 2018;30(2):234-236
No abstract available.
Female
;
Humans
;
Nevus, Pigmented*
;
Pregnant Women*
6.Osteocalcin expression in primary bone tumors: in situ hybridization and immunohistochemical study.
Yong Koo PARK ; Moon Ho YANG ; Youn Wha KIM ; Hye Rim PARK
Journal of Korean Medical Science 1995;10(4):263-268
Osteocalcin is one of the most abundant noncollagenous proteins found in adult bone. It is a highly conserved gamma-carboxyglutamic acid-containing protein that is believed to be produced exclusively by osteoblasts. In this study, intracellular and extracellular localization of osteocalcin in osteosarcoma was examined with anti-osteocalcin antibody and in situ hybridization using a synthetic oligonucleotide. Immunohistochemically, osteoblastic osteosarcomas were all positive for osteocalcin. The chondroblastic osteosarcomas were positive on the neoplastic chondrocytes. The five fibroblastic osteosarcomas out of seven were positive for osteocalcin immunostaining over the neoplastic spindle cells. Five cases of osteoblastic osteosarcomas out of seven were positive for osteocalcin in situ hybridization. Two cases of chondroblastic osteosarcomas and three cases of fibroblastic osteosarcomas were positive for in situ demonstration of osteocalcin. The malignant tumor giant cells were positive for osteocalcin immunostaining 83%. They were also positive for in situ hybridization. The benign giant cells in five giant cell tumors and five aneurysmal bone cysts were negative for osteocalcin immunostaining. The benign giant cells in three chondroblastoma and three Paget's disease were positive for osteocalcin. In this study, the osteocalcin in situ hybridization and immunostaining has very important meaning for making differential diagnoses of, especially giant cell rich bone forming tumors.
Base Sequence
;
Bone Neoplasms/*chemistry
;
Human
;
Immunohistochemistry
;
In Situ Hybridization
;
Molecular Sequence Data
;
Osteocalcin/*analysis
;
Osteosarcoma/*chemistry
7.Treatment with the Pinhole Technique Using Erbium-Doped Yttrium Aluminium Garnet Laser for a Cafe au Lait Macule and Carbon Dioxide Laser for Facial Telangiectasia.
Bo Young CHUNG ; Seung Seog HAN ; Hye Rim MOON ; Mi Woo LEE ; Sung Eun CHANG
Annals of Dermatology 2014;26(5):657-659
No abstract available.
Lasers, Gas*
;
Telangiectasis*
;
Yttrium*
8.Primary Aldosteronism Due to Aldosterone Producing Adenama in the Presence of Contralateral Nonfunctioning Adenama.
Ho Young SON ; Eun Ah KIM ; Jin Il KWON ; Young Joon KIM ; Won Ho CHUNG ; Kyung Rim CHOI ; Sang Jin CHOI ; Hye Young PARK ; Moon Ho KANG
Journal of Korean Society of Endocrinology 1998;13(2):223-229
Primary aldosteronism is in most cases due either to a unilateral adrenal adenama or to a bilateral hyperplasia of the adrenal cortex. But, a few of bilateral adrena1 tumors in primary aldosteronism also have been reported. In these cases, it is important to differentiate the bilateral aldosterone producing adenomas from the unilateral aldosteronoma in the presence of a contralateral nonhmctioning adenoma for marking a treatment plan. We report a case of primary aldosteronism due to a unilateral aldosteronoma in the presence of a contralateral nonfunctioning adenoma. Abdominal CT sean revealed bilateral adrenal tumors, of which the functioning one was successfully localized using adrenal scintigraphy and selective adrenal venous sampling.
Adenoma
;
Adrenal Cortex
;
Aldosterone*
;
Hyperaldosteronism*
;
Hyperplasia
;
Radionuclide Imaging
;
Tomography, X-Ray Computed
9.Clinico-Dermoscopic Features of Atypical Dermatofibroma
Haneul OH ; Hye-Rim MOON ; Hwa-Jung RYU ; Il-Hwan KIM
Korean Journal of Dermatology 2021;59(5):341-347
Background:
Dermatofibroma is a common benign skin neoplasm that is usually easy to recognize; however, in some cases, it is difficult to differentiate it from atypical dermatofibroma. Atypical dermatofibroma is a rare variant of a more aggressive nature and requires complete excision due to its tendency to recur.
Objective:
To describe the clinical and dermoscopic features of dermatofibromas with special emphasis on the characteristics of atypical subtypes and to differentiate them from typical subtypes on the basis of results.
Methods:
We retrospectively searched the databases of patients of Korea University Ansan Hospital from January 2010 to December 2019 who underwent skin biopsies or excision surgeries and had pathological reports of dermatofibroma. Analyses of the clinical characteristics (age, sex, number of lesions, anatomical site) and dermoscopic patterns were performed.
Results:
Dermoscopic patterns were analyzed in 148 cases of dermatofibroma; peripheral delicate pigment networks and central white scar-like patches were the most common patterns found in 45 cases (30.4%). In eight cases of atypical dermatofibroma, three cases (37.5%) showed peripheral homogenous areas and central white networks, followed by multiple white scar-like patches in 2 cases (25.0%), peripheral delicate pigment networks, and central white scar-like patches in 2 cases (25.0%). Dermoscopy revealed a statistically significant difference in the peripheral homogenous area and the central white network pattern between the two groups.
Conclusion
In this study, we analyzed the dermoscopic findings of 148 patients with dermatofibroma and found that the peripheral homogenous area and central white network patterns were significantly more in atypical dermatofibroma.
10.Dermoscopic Findings and the Clinicopathologic Correlation of Pigmented Purpuric Dermatosis:A Retrospective Review of 60 Cases
Ko Eun KIM ; Hye-Rim MOON ; Hwa Jung RYU
Annals of Dermatology 2021;33(3):214-221
Background:
Pigmented purpuric dermatosis (PPD) is known as a chronic recurrent eruption which usually presents with petechiae and pigmented macules on the lower extremities.Dermoscopy is a noninvasive diagnostic tool in identifying pigmented and vascular lesions, which can also be beneficial in the evaluation of PPD.
Objective:
We aimed to analyze the common dermoscopic characteristics of PPD, and correlate those findings with the histopathologic features. Additionally, dermoscopic and pathological findings in this study population were compared with other similar studies from the literature review.
Methods:
A retrospective analysis was performed using data of 60 patients who were diagnosed as PPD by skin biopsy and had dermoscopic examination. The pathologic analysis was performed by categorizing the pattern into lichenoid, perivascular, interface, and spongiotic subtype, and the dermoscopic assessment was performed by the three authors independently.
Results:
In dermoscopy, 96.7% of the patients showed red globules and dots, followed by brownish patch, coppery-red pigmentation, and annular comma-like vessels. The pathologic pattern analysis revealed statistically significant association of lichenoid pattern with coppery red pigmentation, perivascular pattern with annular/comma-like vessels, and spongiosis pattern with reticular pigmented network and linear vessels. The interrater similarity test showed total kappa value of 0.811which referred to “very good”.
Conclusion
In this study, the prevalence of dermoscopic features in Asian PPD patients was identified, which was similar with previous studies. The dermoscopic-pathologic correlation was found in four dermoscopic features. We suggest that dermoscopic examination is helpful in clinical diagnosis and pathological prediction of PPD.