scholarly journals EP16.24: Prenatal diagnosis of a rare case of immature teratoma in the eye

2019 ◽  
Vol 54 (S1) ◽  
pp. 332-332
Author(s):  
X. Chen
Keyword(s):  
Prenatal Diagnosis ◽  
Rare Case ◽  
Immature Teratoma

LUMBOSACRAL WILMS' TUMOR AS A COMPONENT OF IMMATURE TERATOMA ASSOCIATED WITH SPINAL DYSRAPHISM—A RARE CASE AND SHORT LITERATURE REVIEW

2009 ◽  
Vol 28 (5) ◽  
pp. 201-208 ◽  
Author(s):  
Mehar Chand Sharma ◽  
Deepali Jain ◽  
Chitra Sarkar ◽  
Veereshwar Bhatnagar ◽  
Arvind Rishi ◽  
...  
Keyword(s):  
Literature Review ◽  
Rare Case ◽  
Wilms Tumor ◽  
Spinal Dysraphism ◽  
Immature Teratoma

Prenatal diagnosis of congenital immature teratoma arising from retroperitoneum

2006 ◽  
Vol 26 (5) ◽  
pp. 485-487 ◽  
Author(s):  
Ching-Yu Chou ◽  
Chien-Nan Lee ◽  
Jin-Chung Shih
Keyword(s):  
Prenatal Diagnosis ◽  
Immature Teratoma

scholarly journals VP52.06: Prenatal diagnosis of the rare case of diphallia in association with bladder exstrophy

2021 ◽  
Vol 58 (S1) ◽  
pp. 308-308
Author(s):  
H. Vafaei ◽  
S. Roozmeh ◽  
A. Bahador ◽  
M. Zare Khafri ◽  
M. Ghiasi ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Rare Case ◽  
Bladder Exstrophy

scholarly journals A Case of BeckwithWiedemann Syndrome with Polyhydramnios

2017 ◽  
pp. 185
Author(s):  
Yusrawati Yusrawati ◽  
Reno Muhatiah
Keyword(s):  
Birth Weight ◽  
Prenatal Diagnosis ◽  
Caesarean Section ◽  
Apgar Score ◽  
Rare Case ◽  
Obstet Gynecol ◽  
Fetal Distress ◽  
Polycystic Kidney ◽  
Prenatal Diagnostic ◽  
Female Baby

Objective: To report a rare case of Beckwith-Wiedemann Syndrome with polyhydramnios. Methods: Reporting a case of Beckwith-Wiedemann syndrome with polyhydramnios. Results: Case of Mrs. Y, 27 years old woman, G2P1A0L1 preterm pregnancy (30-31 weeks) with polyhidramnios. From ultrasound found renomegaly, bilateral hyperechogenic polycystic kidney, and the karyotype result was 46,XX. Caesarean section was performed due to fetal distress. A female baby was born by caesarean section with birth weight of 1300 grams, 37 centimeters of body length, and APGAR score of 6/8. The congenital anomalies found were hepatomegaly, renomegaly, bilateral hyperechogenic renal polycystic, low set ears. The baby was died in NICU on day care 5th, with suspected of sepsis. Conclusion: Prenatal diagnosis of Beckwith-Wiedemann syndrome on fetus with polyhydramnios. [Indones J Obstet Gynecol 2017; 5-3: 185-188] Keywords: amniocentesis, beckwith-wiedemann syndrome, polyhydramnios, prenatal diagnostic, USG

Rare case of XX/XY mosaicism and trisomy 13 in early prenatal diagnosis

2012 ◽  
Vol 94 (4) ◽  
pp. 245-248 ◽  
Author(s):  
Stavros Sifakis ◽  
Katherine Anagnostopoulou ◽  
Konstantina Plastira ◽  
Nikolaos Vrachnis ◽  
Anastasia Konstantinidou ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Rare Case ◽  
Trisomy 13

Prenatal diagnosis of a huge facial tumor: Report of a rare case and literature review

2012 ◽  
Vol 52 (2) ◽  
pp. 111-114 ◽  
Author(s):  
Zeki Sahinoglu ◽  
Arif Aktug Ertekin ◽  
Aysenur Cerrah Celayir ◽  
Berrin Gucluer
Keyword(s):  
Prenatal Diagnosis ◽  
Literature Review ◽  
Rare Case

scholarly journals Retroperitoneal Immature Teratoma in a Neonate

2017 ◽  
Vol 6 (2) ◽  
pp. 42
Author(s):  
Chiranjiv Kumar ◽  
Rajpal Singh Sisodiya ◽  
Shasanka Shekhar Panda ◽  
Yogesh Kumar Sarin
Keyword(s):  
Rare Case ◽  
Relevant Literature ◽  
Immature Teratoma ◽  
Retroperitoneal Teratoma

We report a rare case of large immature retroperitoneal teratoma in a neonate. The diagnostic and therapeutic challenges of dealing with such a case have been discussed and the relevant literature reviewed.

scholarly journals A rare case of extragonadal immature teratoma mimicking as subserosal pedunculated myoma

2020 ◽  
Vol 9 (6) ◽  
pp. 2649
Author(s):  
Aditi Rai ◽  
Ramesh Bettaiah ◽  
Minal Kumbhalwar ◽  
Isha Rani ◽  
Hema Garlapati
Keyword(s):  
Abdominal Pain ◽  
Rare Case ◽  
Mature Teratoma ◽  
Young Patients ◽  
Immature Teratoma ◽  
Primary Surgery ◽  
Ovarian Cancers ◽  
Histopathologic Diagnosis ◽  
Preservation Of Fertility ◽  
Cell Malignancy

Immature teratomas are usually derived from a malignant transformation of mature teratoma. The pure immature teratoma accounts for less than 1% of all ovarian cancers. It is the second most common germ cell malignancy and accounts for 10-20% of all ovarian malignancies seen in women younger than 20 years of age. Extragonadal origin are extremely rare and the most common extragonadal site of these teratomas is the omentum. We hereby describe a case report of a 29-year-old lady who presented with abdominal pain and her imaging with an ultrasound revealed a mass with features suggestive of a subserosal fibroid. She underwent a laproscopic myomectomy. A histopathologic diagnosis of Immature teratoma was made following her primary surgery. She subsequently underwent a staging laparotomy which was followed by chemotherapy. Immature teratomas predominantly occur in young patients, and preservation of fertility is an important factor in its management. Treatment should be initiated as soon as possible after surgery, preferably within 7-10 days, in those patients who require chemotherapy.

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