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.Testicular Biopsy in Male Sterility.
Korean Journal of Urology 1971;12(1):11-20
No abstract available.
Biopsy*
;
Humans
;
Infertility, Male*
;
Male
;
Male*
5.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*
6.Schwannoma of the Adrenal Gland: A case report.
Yong Chan CHUN ; Sun Hee SUNG ; Chan Il PARK
Korean Journal of Pathology 1993;27(4):424-426
Retroperitoneum is often the site of occurrence of schwannoma, but reports on schwanoma of the adrenal gland is exceptional and only 4 cases have been documented in the literature. This report is to add one such case occurred in a 53 year-old male who had anorexia, nausea and indigestion for one month. Whole body bone scan and abdominal CT scan revealed a 10 cm sized solid mass at upper pole of the left kidney. Under the impression of renal cell carcinoma, an operation was performed. The tumor was well encapsulated and appeared not to involve the kidney. The cut surfaces were light yellow and seemed to be composed of several hard lobules with areas of mucoid, cystic and calcific changes. No adrenal gland was identified grossly. But microscopically, the tumor was found to be partly surrounded by a small portion of adrenal cortical tissue. Histologically the tumor was a typical schwannoma with Verocay bodies, although modified in some extents by mucoid degeneration, cystic change, hyaline change and focal calcification. It is worthwhile to remember that the retroperitoneal schwannoma commonly had a huge size, sometimes involving the adjacent structures.
Male
;
Humans
7.Cystic Adventitial Disease of the Popliteal Artery: A case report.
Soo Min KANG ; Kyeong Cheon JUNG ; Je G CHI
Korean Journal of Pathology 1993;27(4):418-420
Localized cystic degeneration of peripheral arteries represents and unusual cause of arterial insufficiency. It frequently occurs in patient without generalized arteriosclerosis. It has been reported in patients from age 11 to 62 years. Cystic adventitial disease is most common in the popliteal artery. At least 115 cases have been reported worldwide, but none in Korea. We report a case of cystic adventitial disease involving the left popliteal artery. This 64-year-old man presented with an 18-month history of cramping pain of sudden onset in the left calf and claudication. Angiographic findings showed a 6 cm length of luminal obliteration of the popliteal artery. Segmentally resected popliteal artery showed two longitudinally directed cystic masses measuring 3.5x1.5 cm and 2.5x1.5 cm in the adventitia. Microscopic examination revealed cystic space in the arterial adventitia compressing arterial lumen. There were a number of foamy histiocytes collected along the cystic lumen.
Male
;
Humans
8.A Case of Macular Amyloidosis due to Nylon Towel.
Hyung Jun SIM ; Sung Hee KIM ; Ki Seung DOH ; Min Soo JANG ; Kee Suck SUH ; Sang Tae KIM
Korean Journal of Dermatology 2004;42(1):119-121
Amyloidosis is a disorder of protein metabolism characterized by the extracellular deposition of abnormal protein fibrils. We report a case of macular amyloidosis due to nylon towel on his back. A 61-year-old male presented with asymptomatic hyperpigmented macules on the scapulae for 6 years. He had a habit of scrubbing his back for many years with a rough nylon towel while taking a bath. The histologic examination revealed liquefaction degeneration and homogenous eosinophilic deposition in the papillary dermis. In Congo red, amyloid material stained positively and in anti-keratin antibody staining. He had neither clinical nor laboratory evidence of systemic amyloidosis. A diagnosis of friction amyloidosis was made on histological and immunohistopathological findings.
Male
;
Humans
9.A Case of Circumscribed Palmar Hypokeratosis.
Young Il JEONG ; Sung Eun CHANG ; Mi Woo LEE ; Jee Ho CHOI ; Kee Chan MOON ; Jai Kyoung KOH
Korean Journal of Dermatology 2004;42(1):111-113
Circumscribed palmar hypokeratosis is a distinctive disorder characterized by circular area of erythematous depressed skin involving the thenar and hypothenar regions of the palm. We present the case of 66-year-old man with circumscribed palmar hypokeratotic lesion. He developed an acquired, solitary, circumscribed, erythematous, depressed skin on the right palm. Histopathologic study demonstrated a depression of the epidermis, with a sharp stair between normal and involved skin. The epidermis covering the depression showed markedly thinner horny layer and slightly diminished granular cell layer when compared with adjacent noninvolved skin. Serial section failed to demonstrate cornoid lamellae. To our knowledge, this distinctive entity has been previously reported in Korea.
Male
;
Humans
10.Pancreatic Pseudocyst with Splenic Involvement: A Case Report.
Jeong Hwan CHUN ; Han Seong KIM ; Mee JOO ; Sun Hee CHANG ; Ji Eun KWAK ; Sang Hwa SHIM ; Chul Nam KIM ; Soon Joo CHA
Korean Journal of Pathology 2008;42(6):405-408
There have been a few reported cases of pancreatic pseudocyst with involvement of adjacent structures including the stomach, duodenum, and even the mediastinum. An intrasplenic pancreatic pseudocyst is an uncommon complication of acute or chronic pancreatitis. We report a case of pancreatic pseudocyst with splenic involvement in a 69-year-old man with a review of literatures. Abdominal CT revealed a 4 cm sized cyst at the pancreatic tail which was extending into the splenic hilum and splenic parenchyma. Distal pancreatectomy and splenectomy was performed. Pathologic findings demonstrated a pseudocyst of pancreatic tail which communicated with the infacted splenic parenchyma. Also vasculitis, endothelial hyperplasia and medial calcification of the splenic artery were observed.
Male
;
Humans