1.Ectomesenchymal Chondromyxoid Tumor in the Anterior Tongue: Case Report of a Unique Tumor.
Min Gyoung PAK ; Kyung Bin KIM ; Nari SHIN ; Woo Kyung KIM ; Dong Hoon SHIN ; Kyung Un CHOI ; Mee Young SOL
Korean Journal of Pathology 2012;46(2):192-196
Ectomesenchymal chondromyxoid tumor (ECMT) is a rare tumor, exclusively arising in the anterior tongue. Thirty-eight cases have been reported in the English literature. It usually presents as a sessile protrusion and shows round to spindle cells embedded in myxoid to chondroid stroma. Tumor cells are almost always positive for polyclonal glial fibrillary acidic protein (GFAP). We report our experience in the recent treatment of a case of ECMT, the third case in 3 years. The mass in the anterior tongue revealed characteristic morphologic features of ECMT and the expression of polyclonal GFAP. Although ECMT should be differentiated from other mesenchymal tumors including myoepithelioma, its clinical, morphological, and immunohistochemical features enable its diagnosis, especially when pathologists are aware of it.
Glial Fibrillary Acidic Protein
;
Myoepithelioma
;
Tongue
2.Chordoid Glioma: an Uncommon Tumor of the Third Ventricle.
Seong Hyun PARK ; Jeong Hyun HWANG
Journal of Korean Neurosurgical Society 2006;40(1):40-43
Chordoid glioma is an uncommon low-grade tumor of the third ventricle with histologic features of a chordoma and immunolabeling for glial fibrillary acid protein. We present a rare case of a patient with a chordoid glioma of the third ventricle and review the literature regarding this tumor's clinical, radiological and pathologic aspects.
Chordoma
;
Glial Fibrillary Acidic Protein
;
Glioma*
;
Humans
;
Third Ventricle*
3.A Case of Pleomorphic Xanthoastrocytoma.
Journal of Korean Neurosurgical Society 1985;14(2):401-406
The pleomorphic xanthoastrocytoma is considered as a special subgroup of gliomas because of its distinctive characteristics regarding age, gross and microscopic features, and perhaps, most importantly, the relatively favorable prognosis despite of pleomorphism and bizarre giant cells in the microscopic picture. Because of rarity of this disease entity, we report a case of pleomorphic xanthoastrocytoma with a review of literature.
Giant Cells
;
Glial Fibrillary Acidic Protein
;
Glioma
;
Prognosis
4.Congenital Melanocytic Nevus Showing an Unusual Clinical Manifestation.
You Jin YANG ; Yoon Hwan KIM ; Joon LEE ; Dong Hoon KIM ; Hee Jung KIM ; Ga Young LEE ; Won Serk KIM
Korean Journal of Dermatology 2011;49(7):648-651
Completely neurotized melanocytic nevi are often clinically and histologically indistinguishable from neurofibromas. We report a 23-year-old female who presented with a dark brown plaque with an underlying soft blue subcutaneous nodule in the left infra-axillary area. The skin biopsy revealed markedly increased melanocytic proliferation and nests of nevus cells within dermo-epidermal junction and upper dermis. Circumscribed, non-encapsulated tumor of the dermis was composed of loosely-spaced spindle cells and wavy stroma. Spindle cells in the lower dermis showed staining for S-100, but failed to express glial fibrillary acidic protein and Leu-7. We present an interesting case because the lesion presented as a soft blue subcutaneous nodule suggested an underlying hemangioma or neurofibroma initially, but was shown to be a neurotized melanocytic nevus based on immunohistochemical examination.
Biopsy
;
Dermis
;
Female
;
Glial Fibrillary Acidic Protein
;
Hemangioma
;
Humans
;
Neurofibroma
;
Nevus
;
Nevus, Pigmented
;
Skin
;
Young Adult
5.Pleomorphic Xanthoastrocytoma: Report of Three Cases.
Young Jo CHA ; Seong Ho KIM ; Shi Hun SONG ; Kwan Tae KIM ; Kyu Sang SONG ; Youn KIM
Journal of Korean Neurosurgical Society 1993;22(12):1387-1393
Pleomorphic xanthoastrocytoma is known as a rare specialized type of cerebral astrocytoma, which occurs mainly in the temporal loe of the brain in young ages in spite of marked pleomorphism with multinucleated giant cells, lipid-laden xantomatous cells, rich reticulin net-works, and the demonstration of glial fibrillary acidic protein, the prognosis is usually favorable. The authors report three cases of pleomorphic xanthoastrocytoma which were presented with headache and review the past literature.
Astrocytoma
;
Brain
;
Giant Cells
;
Glial Fibrillary Acidic Protein
;
Headache
;
Prognosis
;
Reticulin
6.Adhesion between Amniotic Membrane and Retinal Tissue and Inhibition of Amniotic Membrane on Cell Transformation.
Moon Shin LEE ; Kyung Min LEE ; Sang Hun KIM ; Oh Woong KWON
Journal of the Korean Ophthalmological Society 2003;44(2):459-471
PURPOSE: Tissue adhesion rate between the amniotic membrane and the retinal tissue and histological change of the retinal tissue was studied. And the inhibition effect of amniotic membrane on the retinal pigment epithelial cell transformation was evaluated. METHODS: The human amniotic membrane and the porcine retinal tissue flap were used. The sensory retinal flap and the retinal pigment epithelial flap were placed on the amniotic membrane in culture disk. Tissue adhesion was evaluated and graded at 1, 2, 3, 4 and 5 weeks. Glial fibrillary acidic protein immunohistochemical staining and Masson's trichrome staining were performed for histologic study. Transmitted electron microscope examination was performed to study the stabilization effects of amniotic membrane. RESULTS: Tissue adhesion rates showed no significant change until the 4th week, but tend to decrease in the 5th week of organotissue culture. Tissue adhesion rate was higher in the chorion-side than in the amnion-side culture (p=0.000) and was higher in the retinal pigment epithelial than in the retinal flap (p=0.000). The inhibition of cell transformation was higher in the chorion-side culture than in the amnion-side culture. CONCLUSIONS: Amniotic membrane can be used for prevention of proliferative vitreoretinopathy by its mechanical barrier effect and cell stability effect.
Amnion*
;
Epithelial Cells
;
Glial Fibrillary Acidic Protein
;
Humans
;
Retinal Pigment Epithelium
;
Retinaldehyde*
;
Tissue Adhesions
;
Vitreoretinopathy, Proliferative
7.A Case of Myxoid Neurothekeoma on the Hand.
Dong Jin RYU ; Hee Jung KIM ; Jin Young JUNG ; Yeon Sook KWON ; Ju Hee LEE
Korean Journal of Dermatology 2009;47(8):982-985
Neurothekeoma is a benign dermal soft tissue tumor that is probably of nerve sheath origin. It usually presents as a slow-growing, solitary papule or nodule that is mainly located on the head and neck or upper extremities except for the hand. There are three histologic subtypes - myxoid, mixed and cellular type - depending on the amount of myxoid stroma. Immunohistochemical markers such as S-100, glial fibrillary acidic protein, nerve growth factor receptor, NK1C3 (CD57) and Ki-M1p can be applied to the tumor cells to distinguish among thesethree subtypes of neurothekeoma. Only one case has been previously reported on the hand in Korea. Herein, we report a rare case of myxoid neurothekeoma on the hand with a review of the related literature.
Glial Fibrillary Acidic Protein
;
Hand
;
Head
;
Korea
;
Neck
;
Nerve Growth Factor
;
Neurothekeoma
;
Upper Extremity
9.Significance of the Expression of Tumor Markers in Adenoid Cystic Carcinoma and Pleomorphic Adenoma of the Salivary Gland.
Seong Jun CHOI ; Sung Il CHO ; Nam Yong DO ; Jun Han LEE ; Ji Yoon CHOI ; Sung Chul LIM
Korean Journal of Otolaryngology - Head and Neck Surgery 2008;51(4):336-342
BACKGROUND AND OBJECTIVES: Salivary gland tumors are characterized by extreme histological diversity. Even within a single tumor, various histological patterns are observed. The same histological patterns are shared among various tumor types, regardless of the biological behavior, making diagnosis difficult. Although a great number of immunohistochemical studies of major salivary gland tumors have been published, their clinical and diagnostic implications are not fully apparent. We have performed basic immunohistochemical stains of pleomorphic adenoma (PA) and adenoid cystic carcinoma (ACC) to determine the diagnostic value of c-kit, Ki-67, glial fibrillary acidic protein (GFAP) and p53. MATERIALS AND METHOD: Paraffin-embedded tissue specimens from 48 cases, who were diagnosed as PA (n=31) and ACC (n=17) from 1993 to 2002, were immunohistochemically stained for c-kit, Ki-67, GFAP and p53. RESULTS: In the immunohistochemical stains of c-kit, Ki-67 and p53, there were no difference between PA and ACC. However, in the immunohistochemical stain of GFAP, there were difference in PA and ACC. GFAP was expressed in 74% of the PA and was not expressed in all cases of ACC. CONCLUSION: These data suggest that GFAP immunoreactivity could be helped in the occasional differential diagnostic dilemma of pleomorphic adenoma versus adenoid cystic carcinoma in salivary gland.
Adenoids
;
Adenoma, Pleomorphic
;
Carcinoma, Adenoid Cystic
;
Coloring Agents
;
Glial Fibrillary Acidic Protein
;
Salivary Glands
;
Biomarkers, Tumor
10.Developmental Changes of Glial Fibrillary Acidic Protein (GFAP) and Proliferating Cell Nuclear Antigen (PCNA) Immunoreactivity of the Ependyma lining the Central Canal and Ventriculus Terminalis in the Human Fetus.
Ho Suck KANG ; Dae Yong SONG ; Byung Pil CHO ; Young Chul YANG
Korean Journal of Anatomy 2002;35(3):229-238
The distinguishing morphological features of the ependyma lining ventriculus terminalis in human fetus have suggested that its differentiation would be somewhat delayed or arrested as compared with the ependyma lining central canal. To demonstrate this hypothesis, GFAP was used as a marker to compare the developmental state of the ependyma lining ventriculus terminalis and central canal along fetal age (18 -to 24 -week -old fetuses were investigat-ed). PCNA was also used as a marker to identify whether proliferation potentiality of the ependyma lining ventriculus terminalis lasted longer than that of the ependyma lining central canal as a result of differentiation delay. GFAP -positive ependymal cells were restricted to dorsal plate at central canal but at ventriculus terminalis, many positive cells were identified in all regions compared with the ependyma lining central canal. The number of PCNA -positive ependymal cells lining central canal decreased sharply about the time of 20th week, but at ventriculus terminalis, many ependymal cells continued to express PCNA after 20th week. As a result, we could conclude that differentiation of the ependyma lining ventriculus terminalis is delayed as compared with the ependyma lining central canal. In accordance with its developmental delay, it lasts longer proliferation potentiality than the ependyma lining central canal.
Ependyma*
;
Fetus*
;
Gestational Age
;
Glial Fibrillary Acidic Protein*
;
Humans*
;
Proliferating Cell Nuclear Antigen*