1.Male Infertility.
Korean Journal of Fertility and Sterility 2006;33(1):1-14
No abstract available.
Humans
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Infertility, Male*
;
Male
;
Male*
2.A Clinical Study on Male Sterility.
Korean Journal of Urology 1972;13(3):163-166
No abstract available.
Humans
;
Infertility, Male*
;
Male
;
Male*
3.Evidence based evaluation of the infertile male
Philippine Journal of Reproductive Endocrinology and Infertility 2007;4(1):28-35
The goals of the evaluation is to identify; 1) potentially correctable conditions, 2) irreversible conditions but are amenable to ART using male partner sperm, 3) irreversible conditions not amenable to ART, fro which donor IUI or adoption are possible options, 4) life- or health threatening conditions that may underlie infertility and require medical attention and 5) genetic abnormalities that may affect offspring if ART is employed.
MALE
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INFERTILITY
;
INFERTILITY, MALE
4.Genetic Causes in Male Infertility and Current Studies on Infertility Genes.
Kyung Ho LEE ; Jung Min LEE ; Kun Soo RHEE
Journal of Korean Society of Endocrinology 2001;16(6):550-561
No abstract available.
Humans
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Infertility*
;
Infertility, Male*
;
Male
;
Male*
5.Testicular Biopsy in Male Sterility.
Korean Journal of Urology 1971;12(1):11-20
No abstract available.
Biopsy*
;
Humans
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Infertility, Male*
;
Male
;
Male*
6.Adenoid Cystic Carcinoma of the Lung: Report of 2 cases.
Jae Soo KOH ; Chang Won HA ; Na Hye MYONG ; Kyung Ja CHO ; Mi Kyung KIM ; Ja June JANG
Korean Journal of Pathology 1992;26(2):175-179
Adenoid cystic carcinoma of the lung is histologically and ultrastructurally identical to the salivary gland tumor of the same name and is characterized by infiltrative growth, local recurrence, and usually a prolonged clinical course. We have recently experienced two cases of adenoid cystic carcinoma arising in the lung. Case 1 was a 59 year-old male who presented with cough, fever, and chill of 1.5 months' duration, and case 2 was a 61 year-old male who was incidentally found to have a 3 to 4 cm sized lobulated mass in the right upper lobe. After being worked up, both patients underwent right pneumonectomy. In case 1, a 3x2 cm sized tumor was located in the lower bronchus, partly elevating toward the lumen and partly infiltrating into regional lymph nodes and lung parenchyma showing grayish-white and solid cut surface. Case 2 was a 3.5x3.5 cm sized upper bronchial tumor resembling the former in appearance. Histologically, the tumors were composed of small round hyperchromatic cells, forming solid, cribriform, acinar, or tubular structures. Luminal spaces in tumor cell nests contained PAS-positive mucinous or hyaline material. Among the tumor cells, scattered islands of normal submucosal gland were noticed.
Male
;
Humans
8.Horizontal and Vertical Fusional Amplitudes in Normal Eyes.
Geon Young LEE ; Yong Yeon KIM
Journal of the Korean Ophthalmological Society 1991;32(12):1116-1122
Fusional amplitudes can be measured using various clinical techniques and targets. But the vergence ranges are different according to the used instruments and the environmental conditions. Currently, measurement with the prism is usually llsed but this method have wide vardabele ranges by the used targets and environmental settings. The authors measured the vertical and horizontal fusional amplitudes of 135 normal Korean men with rotary prism in a well-lit office and compared the group using dim light targer with the group using small letter target. In the group using dim light target, true far convergence value was 14.67 +/- 6.24 delta, true far divergence was 6.64 +/- 3.48 delta, true near convergence was 24.96 +/- 7. 33 delta, true near divergence was 11.05 +/- 5.13delta, far vertical vergence was 2.93 +/-0.95 delta, and near vertical vergence was 3.40 +/- 1.15 delta, There was no statistical differences among are groups(p>0.05), and between the groups using small letter target and dim light target in true near and far convergence amplitudes (p>0.05). This study shows that the method using dim light target is simple and valuable method in measuring the fusional vergences.
Humans
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Male
9.Richer's Syndrome: Report of a case.
Su Kyeong YEON ; Chang Sug KANG ; Han Jin LEE ; Dong Uk KIM ; Chun Chu KIM ; Sang In SHIM
Korean Journal of Pathology 1994;28(4):420-426
Richer's syndrome is a development of a high grade malignant lymphoma in a patient with preexisting chronic 1ymphocytic leukemia, small lymphocytic lymphoma or Waldenstrom's macroglobulinemia. A rare case of Richer's syndrome arising in the spleen of a 35-year-old-man was studied by morphology, immunohistochemistry and gene rearrangement study. He has had weight loss and night sweat for last 6 months. Hepatosplenomegaly and abdominal lymphadenopathy were noted on CT scanning. Especially an ovoid radiolucent mass was found within the image of splenomegaly. Lymph nodes and liver biopsy, bone marrow aspiration and splenectomy were done. In the lymph nodes, liver and bone marrow, well differentiated small lymphocytic infiltrations were found but, in the spleen, pleomorphic, large cells with occasional multinucleated giant cells formed a nodular mass surrounded by diffuse, extensive infiltration of small well differentiated lymphocytes. The two distinctive areas in the spleen had positive staining for B-cell marker (HLA-DR and L26), negative staining for T-cell marker (UCLH1), and positive staining for IgM heavy chain and kappa light chain by immuohistochemical study. so this case was diagnosed as a diffuse large cell 1ymphoma transformed from small lymphocytic lymphoma. We made an another effort to clarify their clonality. Gene rearrangement method usingcomplementarity.determining region 3(CDR3) of immunoglobulin heavy chain (IgH) gene and T-cell receptor gamma (TCRgamma) gene by polymerase chain reaction (PCR) technique was done. The two lymphomas in the spleen demonstrated the same rearrangement pattern in both IgH and TCRgamma gene. We think these findings strongly suggest that the large cell lymphoma has the same clonality with that of the small lymphocytic lymphoma.
Male
;
Humans
10.Adenoid Cystic Carcinoma of Skin: A case report.
Eun Duk CHANG ; Young Hee JEE ; Sun Moo KIM
Korean Journal of Pathology 1989;23(3):378-381
A primary skin adenoid cystic carcinoma first described by Boggio in 1975, is one of the rarest type of eccrine sweat gland carcinoma. Histologically, a tumor with typical morphologic features closely resembles adenoid cystic carcinoma was found in other tissues but in the skin must be distinguished from aggressive basal cell carcinoma. The natural history of this tumor is not yet fully determined but suggests a long indolent and progressive course. We report a case of a 77-year-old male with a small skin nodule in the abdomen.
Male
;
Humans