1.A Clinical Study on Male Sterility.
Korean Journal of Urology 1972;13(3):163-166
No abstract available.
Humans
;
Infertility, Male*
;
Male
;
Male*
2.Male Infertility.
Korean Journal of Fertility and Sterility 2006;33(1):1-14
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.A Case of Intradermal Fasciitis of the Scalp.
Myoung Joo KIM ; Sook Hyun BANG ; Myung Hwa KIM ; Hae Young CHOI ; Ki Bum MYUNG
Korean Journal of Dermatology 2004;42(7):889-892
Nodular fasciitis represents reactive fibroblastic or myofibroblastic proliferative lesions which may be misdiagnosed as sarcomas due to the rich cellularity, mitotic activity and variant morphologic pattern. It arises in the subcutaneous tissue, skeletal muscles, and fascia. Uncommon clinical and pathological variants of nodular fasciitis, such as intradermal, intravascular, cranial, ossifying, parosteal and proliferative fasciitis, have been described. We present a 23-year-old man with a one year history of a 2x1.5cm sized hard tender nodule on the scalp which is partially depressed at the margin. Histological examination revealed clusters of spindle cells in a myxoid background, chronic inflammatory cells and extravasated red cells in the dermis. Immunohistochemically, the spindle cells showed positivity of vimentin or smooth muscle actin, and negativity of desmin or S-100 protein. The staining results support its myofibroblastic origin. There is no involved bony lesion on the brain computed tomography (CT). Therefore we report a rare case of intradermal fasciitis arising on the scalp.
Male
;
Humans
7.A Case of Localized Cutaneous Leishmaniasis in A Native Korean.
Yong Ju KIM ; Eul Sang HWANG ; Dong Soo YOO ; Sang Wook SON ; Chang Sub UHM ; Il Hwan KIM
Korean Journal of Dermatology 2004;42(7):884-888
Localized cutaneous leishmaniasis is a chronic ulcerative, usually self-limiting skin disease, and one of the major tropical diseases. This disease is caused by an infection of genus Leishmania, transmitted by a sandfly, and there are some cases of cutaneous leishmaniasis in Koreans after travelling abroad in endemic areas, such as the Middle East and Africa. We report a case of localized cutaneous leishmania in a 70-year-old native Korean man without history of a trip abroad.
Male
;
Humans
8.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
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