2.A Case of Lung Metastasis of Testicular Yolk Sac Tumor.
Ho Ju YOON ; Hyun Kyung CHO ; Jung Sik CHUN ; Chang Kyu OH ; Mahn Kyoo YANG
Journal of the Korean Pediatric Society 1982;25(12):1275-1279
No abstract available.
Endodermal Sinus Tumor*
;
Lung*
;
Neoplasm Metastasis*
;
Yolk Sac*
3.A case of a 45,X,46,X+mar male phenotype mosaic Turner syndrome with a mixed gonadal germ cell tumor
Regrine Bolando Lagarteja ; Brenda Bernadette Bautista-Zamora ; Christian A. Canoy
Philippine Journal of Obstetrics and Gynecology 2023;47(2):81-87
Turner syndrome is a congenital condition affecting 1 in every 2500 female live births. This condition is characterized by complete or partial loss of the X chromosome. They commonly present with normal female external and internal genitalia and may develop hypogonadism and streak ovaries later in life. We describe an unusual presentation of a case of Turner syndrome – a 31-year-old Filipino with male phenotype mosaic Turner syndrome, with 46,X,+mar[46]/45,X[4] chromosome, presenting with ambiguous genitalia and a pelvoabdominal mass. The patient underwent exploratory laparotomy, peritoneal fluid cytology, adhesiolysis, tumor debulking (gonadectomy) appendectomy, omentectomy, identification and inspection of bilateral ureters and bladder, gonioscopy and biopsy of the urogenital cavity (bladder vs. vagina). Histopathology revealed a mixed gonadal tumor, consisting of 70% yolk sac tumor, and 30% dysgerminoma. The patient eventually succumbed to postoperative complications. Postmortem fluorescence-in situ hybridization revealed a 46,X,+mar[46]/45,X,[4].ish der (Y) (DYZ3+), a marker of chromosome Y origin, consistent with a mosaic type Turner syndrome, associated with increased risk for gonadal malignancy.
Dysgerminoma
;
mixed germ cell tumor
;
mosaicism
;
yolk sac tumor
4.Testicular Yolk Sac Tumor in Beckwith-Wiedemann Syndrome.
Beom Jun PARK ; In Yong JEONG ; Dong Woo RO ; Duk Yeon KIM ; Jae Shin PARK
Korean Journal of Urology 1996;37(12):1417-1420
The Beckwith-Wiedemann syndrome, which included congenital anomalies such as macroglossia, exomphalos, postnatal somatic gigantism, have a substantially increased risk for the development of tumor. We report a case of testicular yolk sac tumor associated with Beckwith-Wiedemann syndrome, a previously unreported association. Pathologic examination showed Schiller-Duval body with evidence of testicular yolk sac tumor. This finding appears to represent a previously unreported association between Beckwith-Wiedemann syndrome and testicular yolk sac tumor.
Beckwith-Wiedemann Syndrome*
;
Endodermal Sinus Tumor*
;
Gigantism
;
Hernia, Umbilical
;
Macroglossia
;
Testis
;
Yolk Sac*
5.Small Bowel Obstruction with Strangulation Caused by Patent Omphalomesenteric Duct.
So Hyun NAM ; Yong Ho KIM ; Hyuk Jai JANG ; Yong Pil CHO ; Myeng Sik HAN
Journal of the Korean Surgical Society 2004;67(4):330-333
The vitelline duct is the primitive connection between the yolk sac and embryonic midgut, and undergoes involution between the seventh and ninth weeks of fetal development. A patent omphalomesenteric duct is a form of umbilical remnant with a communication between the umbilicus and intestine that requires surgical resection. Completely patent omphalomesenteric duct is very rare. We here report a case of intestinal obstruction with small bowel strangulation caused by patent omphalomesenteric duct in a 33-year-old man.
Adult
;
Fetal Development
;
Humans
;
Intestinal Obstruction
;
Intestines
;
Umbilicus
;
Vitelline Duct*
;
Yolk Sac
6.A Case of Systemic Chemotherapy in Advanced Yolk Sac Carcinoma.
Kyung Seop LEE ; Choal Hee PARK ; Chun Il KIM
Korean Journal of Urology 1987;28(4):577-581
The majority of testicular tumors in children are of germ cell origin and the predominant pathologic type is the yolk sac carcinoma. Initial treatment of radical orchiectomy is not in question. However, because of its presumed less virulent character, confusion remains as to adjunctive treatment for yolk sac carcinoma. Recently we experienced a case of advanced yolk sac carcinoma treated with multiple systemic chemotherapy regimen.
Child
;
Drug Therapy*
;
Germ Cells
;
Humans
;
Orchiectomy
;
Testicular Neoplasms
;
Yolk Sac*
7.A Case of Gastric Undifferentiated Carcinoma with Focal Yolk Sac Tumor and Hepatoid Carcinoma Differentiation.
Dae Hwa PARK ; Hee Seok MOON ; Dae Hyun TAK ; Suk Hyun KIM ; Jae Gyu SUNG ; Hyun Yong JEONG ; Gyu Sang SONG
The Korean Journal of Helicobacter and Upper Gastrointestinal Research 2013;13(2):114-118
We report herein a case of gastric undifferentiated carcinoma with focal yolk sac tumor and hepatoid carcinoma differentiation. A 57-year-old man was referred after a gastroscopy for anemia evaluation. Gastroscopy revealed an approximately 3 cm ulcerofungating mass occupying the greater curvature of stomach body. Biopsy results revealed a poorly differentiated adenocarcinoma. Left gastric lymph node was enlarged, but there were no evidence of distant metastasis on the abdominal CT. He underwent a radical subtotal gastrectomy and gastroduodenostomy with dissection of the enlarged lymph nodes. Postsurgical histological examination revealed an undifferentiated carcinoma with focal yolk sac tumor and hepatoid carcinoma differentiation. Immunohistochemical staining revealed that the tumor cells were focal positive for AFP, anti-hepatocyte antibody.
Adenocarcinoma
;
Anemia
;
Biopsy
;
Carcinoma
;
Endodermal Sinus Tumor
;
Gastrectomy
;
Gastroscopy
;
Lymph Nodes
;
Neoplasm Metastasis
;
Stomach
;
Yolk Sac
8.A Case of Complete Response by Combination Chemotherapy with BEP Regimen in Endodermal Sinus Tumor of Ovary.
Seung Joon LEE ; Chan Keun LEE ; Sung Yeoh HWANG ; Bong Joo LEE ; Chang Hong KIM ; Heung Gon KIM ; Ki Jung YOON
Korean Journal of Obstetrics and Gynecology 1997;40(11):2581-2584
Endodermal sinus tumors(EST) have also been referred to as "yolk sac tumors" because they are derived from the primitive yolk sac. These lesions are the third most frequent malignant germ-cell tumors of the ovary. Recent advances in treating the endodermal sinus tumor of the ovary with the combination chemotherapy result in improvement of the prognosis. We had experienced a case of the endodermal sinus tumor of 15 year old woman. We report this case with a brief review of literatures.
Adolescent
;
Drug Therapy, Combination*
;
Endoderm*
;
Endodermal Sinus Tumor*
;
Female
;
Humans
;
Ovary*
;
Prognosis
;
Yolk Sac
9.Therapeutic effect and predictors of failure with single-dose methotrexate injection in ectopic pregnancy.
Kyoung Hwa RYU ; Hyun Joo JUNG ; Soon Rye JEON ; Yae Sung CHO ; Youn Ju KIM ; Eun Kyoung CHOI
Korean Journal of Obstetrics and Gynecology 2007;50(9):1260-1269
OBJECTIVE: To evaluate the therapeutic effect of single-dose methotrexate injection for ectopic pregnancy and determine the possible predictors of therapeutic failure. METHODS: We retrospectively reviewed 127 patients' records with methotrexate injection (50 mg/m2) for unruptured ectopic pregnancy from January 2001 to December 2006. The transvaginal sonographic findings in each case were analyzed according to the presence and size of an ectopic mass, endometrial pattern, amount of intraperitoneal fluid, presence of yolk sac and presence of pseudogestational sac. Patient's age, pretreatment beta-hCG levels and clinical symptoms were also recorded. Success of treatment was regarded only when single or another dose of methotrexate injection was needed to lower the beta-hCG levels to non-pregnant state (<5 mIU/ml). RESULTS: Of 127 patients, 65 cases (51.2%) succeeded with single-dose of methotrexate, 44 cases (34.6%) multi-dose of methotrexate, and ultimately 18 cases (14.2%) surgical procedures. Elevated pretreatment beta-hCG levels, size of an ectopic mass, trilaminar endometrial pattern, presence of yolk sac and vaginal bleeding were the main predictors of single-dose methotrexate treatment failure. CONCLUSION: Single-dose methotrexate injection was proved to be safe and effective method for ectopic pregnancy. Transvaginal sonographic findings could be important prognostic factors as well as pretreatment beta-hCG levels.
Female
;
Humans
;
Methotrexate*
;
Pregnancy
;
Pregnancy, Ectopic*
;
Retrospective Studies
;
Treatment Failure
;
Ultrasonography
;
Uterine Hemorrhage
;
Yolk Sac
10.Primary Yolk Sac Tumor of the Cerebellar Hemisphere: Case Report.
Seung Ho YANG ; Yong Kil HONG ; Joon Ki KANG ; Moon Chan KIM
Journal of Korean Neurosurgical Society 2003;33(4):419-421
Primary intracranial yolk sac tumor usually arises in the pineal or suprasellar area and shows poor prognosis. Several children with primary yolk sac tumor in the cerebellum have been reported in the literature, and none of these survived beyond 30 months. We report a case of primary yolk sac tumor in the cerebellum showing longer survival with intensive multimodal combined therapy using surgery, preirradiation chemotherapy, and irradiation.
Cerebellum
;
Child
;
Drug Therapy
;
Endodermal Sinus Tumor*
;
Humans
;
Prognosis
;
Radiotherapy
;
Yolk Sac*