- Laryngeal Atresia with Tracheoesophageal Fistula: 1 case report
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Kim EK, Chi JG
- KMID: 1724732
- Korean J Pathol.
- 1993 Oct;27(5):504-508.
Laryngeal atresia is a very rare congenital anomaly requiring immediate tracheotomy. We present a case of laryngeal atresia with tracheoesophageal fistula who showed immediate respiratory difficulty after ligation of umbilical... -
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- Malignant Eccrine Acrospiroma: A case report
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Han GR, Kim IS, Song KY, Kim KD, Yeom BW, Choi JS
- KMID: 1724739
- Korean J Pathol.
- 1993 Oct;27(5):538-541.
A case of malignant eccrine acrospiroma of the anterior chest wall is reported. This mass had been present for 20 years and during rescent 5 years it showed frequent ulceration... -
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- Lipoleiomyoma of the Uterus: A case report
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Kang MS, Maeng YH, Park JH, Kim YW, Lee JH, Yang MH
- KMID: 1724738
- Korean J Pathol.
- 1993 Oct;27(5):535-537.
A rare case of uterine lipoleiomyoma is reported with presentation of computed tomography, histomorphologic and immunohistochemical findings. This tumor is predominantly lipomatous with an admixture of smooth muscle fiber and... -
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- Papillary Eccrine Adenoma: Histopathological and Immunohistochemical study
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Park CK
- KMID: 1724735
- Korean J Pathol.
- 1993 Oct;27(5):518-523.
Papillary eccrine adenoma is a rare benign sweat gland neoplasm. However, it can show locally aggressive clinical course when it is incompletely removed. A case of papillary eccrine adenoma of... -
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- Nongestational Choriocarcinoma of the Overy
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Kang JH, Lee HJ, Lee SK
- KMID: 1724734
- Korean J Pathol.
- 1993 Oct;27(5):514-517.
Most instances of choriocarcinoma of the ovary are gestational in origin. In contrast, nongestational choriocarcinoma of the ovary is an exceedingly rare primary germ cell neoplasm that has worse prognosis... -
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- Right Atrial Myxoma Showing Granulomatous Lesion with Pulmonary Infart: A case report
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Song KC, Jung SH, Shin DH
- KMID: 1724731
- Korean J Pathol.
- 1993 Oct;27(5):501-503.
Cardiac myxoma is the most common primary tumor of the heart. The tumor contains a variety of cell types that are thought to arise from a focus of primitive pluripotential... -
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- Cellular Blue Nevus: A case report
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Myong NH, Chi JG, Cho BK, Song KY
- KMID: 1724740
- Korean J Pathol.
- 1993 Oct;27(5):542-545.
Cellular blue nevus is an benign variant of blue nevus group, characterized by cellular islands composed of closely aggregated spindle cells with little or no melanin. The other variants include... -
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- Chromomycosis of the Skin: A case report
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Kim TS, Song KY, Chi JG
- KMID: 1724737
- Korean J Pathol.
- 1993 Oct;27(5):531-534.
Cutaneous chromomycosis is a slow growing verrucous skin infection caused by five species, identified as Philadophara verruscosa, Fonsecaea dermatitidis, Fonsecaea pedrosoi, Fonsecaea compactum, Cladosporium, carionii. We report a case of... -
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- Scanning Electron Microscopic Findings of Hair Anomalies
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Yoon CJ, Chi JG, Chung HW
- KMID: 1724730
- Korean J Pathol.
- 1993 Oct;27(5):491-500.
Scanning electron microscopic(SEM) examination of hair is an efficient and definite method for the diagnosis of hair anomaly. The Hair specimen is placed on a stub, gold coated, and directly... -
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- Expression of ras Oncogene Product, MHC class II Antigen and Human Papillomavirus 16/18 DNA in Carcinomas of the Uterine Cervix
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Cho KJ, Jang JJ
- KMID: 1724729
- Korean J Pathol.
- 1993 Oct;27(5):485-490.
Immunohistochemical study for ras oncogene product(p21) and MHC class II(HLA-DR) antigen, and in situ hybridization for human papillomavirus(HPV) type 16/18 were performed on 50 squamous cell carcinomas of the uterine... -
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- Congenital Bronchopulmonary Foregut Malformation: Analysis of the surgical and autopsy cases
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Park SH, Chi JG
- KMID: 1724727
- Korean J Pathol.
- 1993 Oct;27(5):459-467.
Because early embryonic development of the tracheobronchial tree and foregut are closely associated, there is a wide spectrum of congenital anomalies involving either one or both organ systems. We analysed... -
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- Primary Oxalosis: A case report
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Song SY, Chi JG, Choi Y, Kim SJ
- KMID: 1724733
- Korean J Pathol.
- 1993 Oct;27(5):509-513.
Primary oxalosis is a rare genetic disorder caused by a deficiency of the peroxisomal enzyme alanine-glyoxylate aminotransferase(type I) and D-glyceric dehydrogenase(type II). It is characterized by the triad of radiopaque... -
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- Apoptosis Induced by Adriamycin in HeLa Cells
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Kim SY, Lee SS
- KMID: 1724725
- Korean J Pathol.
- 1993 Oct;27(5):433-442.
This study was carried out to demonstrate the mode of ADR-induced cell death(apoptosis) on the light and electron microscopic features, to measure the apoptotic index dependent on various doses of... -
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- Optic Nerve Glioma with Neurofibromatosis
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Myong NH, Lee SS, Shu YL, Chi JG
- KMID: 1724736
- Korean J Pathol.
- 1993 Oct;27(5):524-530.
Optic nerve gliomas manifest either as a solitary form or a component of von Recklinghausen's neurofibromatosis. The reported incidence of coexistence with neurofibromatosis varies from 12% to 70%. Usually there... -
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- Sequential Ultrastructural Change of Chorionic Villi in Human Placenta by Gestational Period
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Park TD, Kwon TJ, Chi JG
- KMID: 1724728
- Korean J Pathol.
- 1993 Oct;27(5):468-484.
A study was performed to observe the sequential morphological change of the human placental barrier by means of light microscopy, immunohistochemistry, scanning electron microscopy and transmission electron microscopy. The examined... -
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- Detection of Numerical Chromosomal Aberration in Squamous Cell Carcinoma of the Lung by In Situ Hybridization Using #17 Centromeric Probes
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Lee SS, Han SB, Park SK
- KMID: 1724726
- Korean J Pathol.
- 1993 Oct;27(5):443-458.
This study was carried out to understand the relationship between specific chromosome changes and their phenotypic consequences at the tissue level of human lung cancers. Then paraffin-embedded human lung squamous... -
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