1.A Case of Paratesticular Embryonal Rhabdomyosarcoma.
Sinn JEONG ; Won Joon BHANG ; Tae Hyung RHO ; Young Chul YOON ; Soo Chan KIM ; Sam Keuk NAM
Korean Journal of Urology 2000;41(11):1415-1417
No abstract available.
Rhabdomyosarcoma, Embryonal*
2.Embryonal Rhabdomyosarcoma of the Prostate.
Korean Journal of Urology 1977;18(3):251-257
Embryonal rhabdomyosarcoma of the prostate is a rare and highly malignant disease. We experienced three cases of embryonal rhabdomyosarcomas in recent years, and they were clinically studied.
Prostate*
;
Rhabdomyosarcoma, Embryonal*
3.Embryonal rhabdomyosarcoma of the mandible
Romeo L Villarta ; Erasmo Gonzalo DV Llanes ; Rodante A Roldan
Philippine Journal of Otolaryngology Head and Neck Surgery 2006;21(1-2):36-38
Objectives: 1] To describe a case of an embryonal rhabdomyosarcoma presenting as al radiolucent mandibular mass in a 3-year-old child. 2] To review existing literature on the clinical picture and pathophysiology of intraosseous rhabdomyosarcoma. 3] To identify learning points in the diagnosis of intraosseous rhabdomyosarcoma. Design: Case report. Setting: A tertiary referral hospital. Patients: One (1) Results: A case of a 3-year-old child with a radiolucent mandibular mass is described. Thel final histopathologic report turned out to be embryonal rhabdomyosarcoma. Intraosseous rhabdomyosarcomas are rare occurrences (3.5 percent in one review), and clinically present in younger age groups, with a non-tender, enlarging, firm-hard mass over a specific area. A review of the available literature on intraosseous rhabdomyosarcomas, and its proposed pathogenesis, is presented. Conclusion: A case of a radiolucent mandibular mass in a 3-year-old child is presented. Intraosseous rhabdomyosarcomas of the mandible are rare occurrences that pose challenges to the otorhinolaryngologist. Taken separately, the presentation, patient characteristics, clinical course, ancillary laboratories and imaging modalities may lead even the most astute otorhinolaryngologist astray. The whole clinical picture should be taken together so that the correct diagnosis will not be missed despite the rare presentation. (Author)
RHABDOMYOSARCOMA RHABDOMYOSARCOMA
;
EMBRYONAL
4.Two Cases of Extragonadal Embryonal Carcinoma Originating in Unusual Sites.
Young Seob MIN ; Dong Soo PARK ; Sun Won HONG ; Seong Jun HONG ; Jin Moo LEE
Korean Journal of Urology 1995;36(7):779-783
Primary germ cell tumor of extragonadal origin are rare, accounting for approximately 3 to 5 percent of all germ tumors. Extragonadal germ cell tumors usually originate in midline body structures. We report a case of extragonadal germ cell tumor from the left superficial inguinal area, a nonmidline structure and a case of from the superficial suprapubic area unusual site of extragonadal germ cell tumor-with brief of the literature.
Carcinoma, Embryonal*
;
Germ Cells
;
Neoplasms, Germ Cell and Embryonal
5.A Case of Malignant Mixed Mullerian Tumor of Uterus.
Sang Wook BAI ; See Yong KIM ; Yoon Ho LEE ; Dong Hoon WHANG
Korean Journal of Gynecologic Oncology and Colposcopy 1993;4(4):118-122
A Malignant mixed miillerian tumor of uterus is rare and highly malignant containing epithelial and mesenchymal components. A case of mixed germ cell tumor was exprienced and presented with a brief review of concerned literature.
Neoplasms, Germ Cell and Embryonal
;
Uterus*
6.Embryo carcinoma in a premature teratoma after peritonea (diagnosis and treatment)
Journal of Practical Medicine 2004;474(3):4-7
A case of a woman aged 42 years old with abdomen pain under the navel and bilateral pelvis tumors indentified by CT scanner as post-peritoneal tumors and AFP level increased was treated at Viet Duc hospital with the diagnosis of embryonary carcinoma based on a mature malignant teratoma. Some aspects of the diagnosis and treatment of post-peritoneal teratoma with embryonary carcinoma were received. Authors concluded that up to now in adults for post peritoneal tumor under the group of germ cell tumors, the treatment of choice is a surgery of through removal of the tumor, then the formula of BEP, PEL or VAC chemiotherapy will be carried.
Carcinoma, Embryonal
;
Teratoma
;
Diagnosis
;
Therapeutics
7.A Large Testicular Tumor: A Case Report.
Korean Journal of Urology 1970;11(1):43-45
A case of a 20-year old Korean adolescent who had large (child-head sized) embryonal carcinoma of left testis was presented. Literature was also briefly reviewed.
Adolescent
;
Carcinoma, Embryonal
;
Humans
;
Testis
;
Young Adult
8.A Case of Primary Ovarian Choriocarcinoma.
Kwang Hwa AHN ; Chi Seok AHN ; Pyl Ryang LEE ; Hak Soon KIM ; Jae Ho EARM
Korean Journal of Gynecologic Oncology and Colposcopy 1994;5(2):92-97
Pure, nongestational ovarian choriocarcinomas is extremely rare. Most ovarian choriocarcinoma are combined with other malignant germ cell tumors or can arise as a metastaais from a primnry gestational choriocarcinoma. We experienced a case of primary ovarian choriocarcinoma that probably was associated with a past history of the mixture of germ cell tumor and present it with a review of literature.
Choriocarcinoma*
;
Female
;
Neoplasms, Germ Cell and Embryonal
;
Pregnancy
9.Germ Cell Tumors.
Korean Journal of Pediatrics 2004;47(Suppl 2):S463-S467
No abstract available.
Germ Cells*
;
Neoplasms, Germ Cell and Embryonal*
10.Korean Society for Pediatric Neuro-Oncology Protocol for Germ Cell Tumors.
Korean Journal of Pediatric Hematology-Oncology 2005;12(2):201-218
No abstract available.
Germ Cells*
;
Neoplasms, Germ Cell and Embryonal*