1.Glomerular Basement Membrane Thickness in Minimal Change Disease.
Yoon Mee KIM ; Soon Hee JUNG ; Hyeon Joo JEONG
Korean Journal of Pathology 2000;34(12):994-1000
The thickness of the glomerular basement membrane may vary not only in glomerular disease, but also in normal persons according to age and sex. But there has been no data on the normal thickness of the basement membrane in Korea. This study was designed to determine the glomerular basement membrane thickness as a reference value according to age and sex, in 50 cases of minimal change disease obtained from patients aged 2~67 years. Measurement of glomerular basement membrane was made on electron micrograph using an image analyzer. The thickness of each case was estimated by the arithmetic and harmonic mean methods. The mean thickness of the glomerular basement membrane was 291.9 47.9 nm by harmonic mean method and 284.2 43.7 nm by arithmetic mean method. And the harmonic mean thickness of the glomerular basement membrane according to age was 249.1 32.5 nm (1~5 years), 256.6 45.3 nm (6~10 years), 279.2 57.9 nm (11~15 years), 303.2 43.8 nm (16~20 years), 335.3 37.5 nm (21~30 years), and 291.1 22.5 nm (over 30 years), respectively. There was a trend that the thickness of glomerular basement membranes increased with the age till 30 years of age. There was no significant sex-related difference. In conclusion, the mean glomerular basement membrane thickness is comparable to the data from western people and shows a trend of increasing thickness according to the age.
Basement Membrane
;
Glomerular Basement Membrane*
;
Humans
;
Kidney
;
Korea
;
Nephrosis, Lipoid*
;
Reference Values
2.Histologic Discrepancy between Gastric Biopsy and Resection Specimen in the Era of Endoscopic Treatment for Early Gastric Cancer.
The Korean Journal of Gastroenterology 2014;64(5):256-259
Endoscopic resection (ER) is accepted as a treatment option for early gastric cancer in patients with negligible risk of lymph node metastasis. Determination of histologic differentiation of adenocarcinoma based on pretreatment endoscopic biopsy is critical in deciding the treatment strategy of ER versus surgical resection. However, discrepancies are frequent between pretreatment biopsies and ER specimens, which may result in an additional gastrectomy after ER. In this context, a review on possible factors contributing to the diagnostic discrepancy in the histologic difference between the pretreatment biopsy and ER is necessary. Two major factors are significantly associated with this discrepancy: pathologic characteristics of the tumor itself, i.e. histologic heterogeneity (tumor factor), and diagnostic procedure performed by endoscopists or pathologists (human factor). In this review, we focus on pathologic report of pretreatment biopsy specimens and its clinical significance.
Adenocarcinoma/*pathology
;
Biopsy
;
Cell Differentiation
;
Gastrectomy
;
Gastric Mucosa/pathology
;
Gastroscopy
;
Humans
;
Stomach Neoplasms/*pathology
3.Congenital Cystic Disease of the Kidney overview and a classification.
Mee JOO ; Yeon Mee KIM ; Chong Jai KIM ; Yeon Lim SUH ; Jeong Wook SEO ; Je Geun CHI
Korean Journal of Pathology 1997;31(3):233-243
The congenital renal cystic disease encompasses a complex group of pathologic and clinical entities. We retrospectively reviewed 42 cases of congenital renal cystic lesions classified into four Potter types in a series of 2,063 consecutive autopsies from 1981 to 1996. According to our study based on morphologic, clinical, genetic features and associated anomalies, type I and III are relatively compatible with Potter's original definition. However, it was reasonable that type II and IV are classified to the same group because of: 1) very similar histologic findings representing dysplastic kidney, 2) many associated anomalies, 3) no evidence of inheritance, and 4) presence of a combined type. Syndrome associated cysts, such as Meckel-Gruber syndrome, were also separately classified. If the dysplastic evidence was insufficient for diagnosis to the dysplastic kidney in type II and IV, then these cases would be better classified into a cystic disease associated with congenital hydronephrosis. We propose a classification of the congenital cystic disease of the kidney to be: 1) dysplastic kidney, 2) cystic disease associated with congenital hydronephrosis, 3) polycystic kidney, and 4) syndromic cystic disease.
Autopsy
;
Classification*
;
Diagnosis
;
Hydronephrosis
;
Kidney*
;
Polycystic Kidney Diseases
;
Retrospective Studies
;
Wills
4.Etiologic studies in amenorrhea.
Hyeon Gyeong CHOI ; Sung Hee JUNG ; Cung Suk KIM ; Soo Mee LEE ; Hyeon Joo KIM
Korean Journal of Obstetrics and Gynecology 1993;36(7):1571-1576
No abstract available.
Amenorrhea*
;
Female
5.Incidentally Founded Biphasic Pulmonary Blastoma.
Nam Hoon KIM ; Dong oon KEUM ; Joo Heon KIM ; Mee Ja PARK
Tuberculosis and Respiratory Diseases 2001;50(5):641-644
Pulmonary blastoma is a family of tumors in which the glands or mesenchyme composing the neoplasm are primitive or embryonic in appearance. There are three subtypes, which include well differentiated fetal adenocarcinoma (pulmonary endodermal tumor), biphasic pulmonary blastoma, and cystic and pleuropulmonary blastomas in children. Among them, biphasic pulmonary blastoma is a primary malignancy of the lung originating from multipotential pulmonary blastema including both the malignant fetal epithelial and mesenchymal components. These make up 0.25 to 0.5 percent of all primary malignant lung tumors. This tumor is usually symptomatic and appears as a large, solitary peripheral mass, with a tendency to favor the upper lobe. Here we report a case where small sized asymptomatic peripheral lung mass was diagnosed as a biphasic pulmonary blastoma, prior to the operation, A subsequent percutaneous needle biopsy was performed, which revealed features of a large cell neuroendocirne tumor. In addition, a review of the relevant literature is provided.
Adenocarcinoma
;
Biopsy, Needle
;
Child
;
Endoderm
;
Humans
;
Lung
;
Mesoderm
;
Pulmonary Blastoma*
6.Expression Patterns of S100A6 Gene in Human Thyroid Diseases.
Joo Heon KIM ; Jae Wha KIM ; Seon Young YOON ; Jong Hyuck JOO ; In Seong CHOI ; Mee Ja PARK
Korean Journal of Pathology 2000;34(11):934-940
S100A6 (calcyclin) is a member of the S100 family and has been originally isolated from the cDNA library of Syrian baby hamster kidney cells. The S100A6 gene expression is reported to remain high throughout the cell cycle following induction by serum or growth factors, suggesting that the gene may be required for cell cycle progression. Nevertheless, the role that S100A6 may play in tumor progression remains unknown. In this study, we have explored the expression patterns of S100A6 gene in human thyroid tissues by northern blot analysis. Using the S100A6 monoclonal antibody, we carried out the immunohistochemical staining to determine the distribution/localization of S100A6 protein within tumor or non-tumorous cells of the thyroid. To modulate the regulation of endogenously expressed S100A6 protein in the intracellular level, overexpressed or anti-sense treated transfectant was constructed by using the eukaryotic expression vector. As a result, immunohistochemistry for S100A6 showed a strong positivity in the malignant tumors of thyroid and a high expression level of S100A6 protein affected cell proliferation in the overexpressed transfectant. These findings suggest that S100A6 may be involved in the tumor pathogenesis and provides another parameter for the differentiation of malignant and benign lesions. A well defined monoclonal antibody against S100A6 protein is now available for the immunohistochemical studies of the various thyroid tissues.
Animals
;
Blotting, Northern
;
Cell Cycle
;
Cell Proliferation
;
Cricetinae
;
Gene Expression
;
Gene Library
;
Humans*
;
Immunohistochemistry
;
Intercellular Signaling Peptides and Proteins
;
Kidney
;
Thyroid Diseases*
;
Thyroid Gland*
7.Cellular Schwannoma Arising in a Facial Nerve.
Mee JOO ; Hye Sung KIM ; Yun Kyung KANG ; Hye Kyung LEE ; Jae Young PARK
Korean Journal of Pathology 1997;31(7):688-691
Cellular schwaninoma is a variant of schwannoma, which is characterized by predominance of cellular Antoni A area, presence of mitotic activity, nuclear hyperchromasia, pleomorphism, and absence of Verocay body. These pathologic features often prompted a misdiagnosis of malignancy. However, the clinical outcome has indicated the benignity of the tumor. We have experienced a case of cellular schwannoma arising from right facial nerve with right hemifacial weakness and erosion of mastoid process. Grossly, it was a 3.5 x 3 cm sized and relatively well encapsulated mass with yellowish, friable cut surface. Microscopically, cellular growth with moderate cellular pleomorphism and some mitotic activity (5/40 HPFS, up to 2/HPF) were noted. Immunostaining for S-100 protein showed diffuse strong positive reaction.
Diagnostic Errors
;
Facial Nerve*
;
Mastoid
;
Neurilemmoma*
;
S100 Proteins
8.A case of multiple endobronchial hamartomas.
Sung Kyu PARK ; Kyoung Joo RHEE ; Mee Ja PARK ; Sun Young KIM
Tuberculosis and Respiratory Diseases 1992;39(1):83-88
No abstract available.
Hamartoma*
9.A Case of Papillary Eccrine Adenoma.
Sung Pil YOON ; Seong Hun LEE ; Joo Heung LEE ; Seung Chul LEE ; Joon Mee KIM
Annals of Dermatology 1997;9(2):163-166
Papillary eccrine adenoma is a rare sweat gland tumor with a characteristic histopathological appearance and has a benign clinical course. Five cases were reported in Korea since a report by Song et al. in 1988. We report a case of papillary eccrine adenoma in a 38-year-old male who had a firm, dark brown nodule on the medial surface of the left thigh. Microscopically, the tumor was composed of multiple dilated ducts lined by two or more layers of epithelial cells and the luminal cells showed papillary projections into the lumen in some tubules. Immunoperoxidase staining was positive for CEA, S-100, and EMA. We excised the lesion completely and no evidence of recurrence was observed for 6 months.
Adenoma*
;
Adult
;
Epithelial Cells
;
Humans
;
Korea
;
Male
;
Music
;
Phenobarbital
;
Recurrence
;
Sweat Glands
;
Thigh
10.Cytopathologic Observation of Primary Malignant Melanoma of the Lung: A case report.
Yun Mee KIM ; Jong Hee NAM ; Min Cheol LEE ; Joo Yong YOO ; Kyu Hyuk CHO
Korean Journal of Pathology 1991;25(4):367-375
The pulmonary cytology has reached a high level of accuracy. By the examination of the sputum and/or bronchial brushings, it is now possible to make a diagnosis in 70% to 90% of patients with cancer. Primary melanoma of the lung is very rare and there have been reported about 20 cases in the world literature. We present a case of primary malignant melanoma of the lung in a 61-year-old male diagnosed by cytologic examination of sputum, bronchial brushing and aspirated pleural fluid. Histologic examination of bronchoscopic biopsy and examination of the skin and other primary sites confirmed the diagnosis.
Male
;
Humans
;
Biopsy