1.Male Infertility.
Korean Journal of Fertility and Sterility 2006;33(1):1-14
No abstract available.
Humans
;
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
;
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
;
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
;
Infertility, Male*
;
Male
;
Male*
6.Synovial Sarcoma of the Parietal Pleura: One case report.
Seock Yeol LEE ; In Hag SONG ; Seung Jin LEE ; Hyung Joo PARK ; Cheol Sae LEE ; Kihl Rho LEE
The Korean Journal of Thoracic and Cardiovascular Surgery 2005;38(6):454-456
A 34-year-old male was admitted to our hospital complaining of chest pain. Chest computerized tomography showed pleural effusion and mass in left lower area. After open thoracotomy and mass removal originating from the parietal pleura were done. The mass was pathologically diagnosed as poorly differentiated synovial sarcoma. Synovial sarcoma of the pleura is rare. Herein we report a case of synovial sarcoma of the parietal pleura.
Male
;
Humans
7.Actinomycosis of the Penile Shaft Coexisting with Fibrous Pseudotumor of the Testis.
Eun Jung CHA ; Kyu Yun JANG ; Ho Sung PARK ; Jong Kwan PARK ; Chang Seop LEE ; Myoung Ja CHUNG ; Woo Sung MOON ; Dong Geun LEE ; Myoung Jae KANG
Korean Journal of Pathology 2008;42(1):50-53
Here, we present an uncommon case of the penile shaft actinomycosis with coexisting fibrous pseudotumors of the testis. A 37-year-old, circumcised man presented with one penile and eight scrotal masses. The penile mass having a healed surface ulceration was located at the right side of the penile shaft. It was relatively circumscribed without a fibrous capsule. The cut surface showed a yellow-brown color with central focal necrosis. The scrotal tumors were circumscribed, whorled, white masses 0.3-2.0 cm in diameters, and were attached to the tunica vaginalis and tunica albuginea. Microscopically, the penile mass showed active inflammatory changes containing actinomyces displaying characteristic sulfur granules. Testicular masses were fibrous pseudotumors composed of bland spindle and stellate cells lying in dense collagenous stroma. Actinomycosis of the penis has been reported to occur at the corona of the uncircumcised penis associated with pilonidal sinus. The present case was not associated with pilonidal sinus and, unusually, displayed co-existence with fibrous pseudotumors of the testis.
Male
;
Humans
8.Dedifferentiated Chordoma: Report of a case.
Sang Yong SONG ; Mi Kyung KIM ; Yong Il KIM
Korean Journal of Pathology 1993;27(3):256-262
Dedifferentiated chordoma is a rare pathologic entity presenting an additional sarcomatous component in otherwise classical chordoma. It has been also emphasized that this neoplasm is classified as a distinct entity because of its different clinical settings and aggressive behavior. Dedifferentiation is a peculiar phenomenon but its histogenesis has remained controversial. A 50-yera-old man developed a huge tumor mass in the retrorectal, presacral area, featured with two histological components. The one was a typical chordoma accounted for approximately 60% of the mass and the other was made up of highly cellular, plemorphic, undifferentiated tumor cells, reminiscent partly to the cells of plemorphic malignant fibrous histiocytoma. Ultrastructural features and immunoreactivity against cytokeratin, S-100 protein and alpha-1-antichymotrypsin in both portions support that histologically different components of this neoplasm derive from the same origin. To our knowledge, this is the first case of dedifferentiated chordoma in Korea.
Male
;
Humans
9.Diffuse Embryoma of the Testis: A Case Report.
Korean Journal of Pathology 2008;42(2):103-107
Diffuse embryoma of the testis is a very rare, distinct form of mixed germ cell tumor. I report here on a case of diffuse embryoma in a 22-year-old male who presented with painful scrotal swelling. The resected testis was entirely occupied by a non-encapsulated tumor mass. The cut surface of the tumor was grey or whitish pink, soft and granular with foci of hemorrhage and necrosis. Microscopically, the tumor was characterized by a diffuse, orderly arrangement of embryonal carcinoma and yolk sac tumor in almost equal proportions. The yolk sac tumor component was diffusely wrapped around the embryonal carcinoma. Syncytiotrophoblasts were scattered throughout the tumor. Minor foci of immature teratoma, seminoma and intratubular germ cell neoplasia were observed. The yolk sac tumor (YST) component was emphasized by immunoreactivity for alpha fetoprotein, whereas the embryonal carcinoma was reactive for CD30. The strong reactivity for cytokeratin in the YST component formed an outstanding contrast to the weak cytokeratin reactivity in the embryonal carcinoma.
Male
;
Humans
10.Sacrococcygeal Nodule in a Young Male Patient.
Hyo Sang SONG ; Hee Young KANG
Annals of Dermatology 2014;26(6):771-773