scholarly journals Gliomatosis peritonei with 18F-fluorodeoxyglucose accumulation and contrast enhancement secondary to immature teratoma: A case report

2018 ◽  
Author(s):  
Tsutomu Ohara ◽  
Koji Yamanoi ◽  
Yoshihide Inayama ◽  
Jumpei Ogura ◽  
Mie Sakai ◽  
...  
Keyword(s):  
Case Report ◽  
Contrast Enhancement ◽  
Immature Teratoma ◽  
Gliomatosis Peritonei ◽  
18F Fluorodeoxyglucose

Immature teratoma of gallbladder associated with gliomatosis peritonei, a case report

2007 ◽  
Vol 42 (10) ◽  
pp. e25-e27 ◽  
Author(s):  
Motofumi Torikai ◽  
Hiroyuki Tahara ◽  
Tatsuru Kaji ◽  
Ryuichi Shimono ◽  
Tsunehiro Yano ◽  
...  
Keyword(s):  
Case Report ◽  
Immature Teratoma ◽  
Gliomatosis Peritonei

scholarly journals Gliomatosis Peritonei Arising in Setting of Immature Teratoma of Ovary: A Case Report and Review of Literature

2015 ◽  
Vol 66 (3) ◽  
pp. 192-195 ◽  
Author(s):  
Nisha Marwah ◽  
Ashima Batra ◽  
Sumiti Gupta ◽  
Savita Rani Singhal ◽  
Rajeev Sen
Keyword(s):  
Case Report ◽  
Immature Teratoma ◽  
Review Of Literature ◽  
Gliomatosis Peritonei

Giant Immature Teratoma of the Ovary with Gliomatosis Peritonei in a 15-Year-Old Girl: A Case Report and Literature Review

2014 ◽  
Vol 30 (4) ◽  
pp. 222-226
Author(s):  
Awanindra Kumar ◽  
Prashant Goyal ◽  
Shelly Sehgal ◽  
Soumyesh Ghosh ◽  
Vinita Kumar ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Immature Teratoma ◽  
Gliomatosis Peritonei

scholarly journals Synchronous primary malignancy of ovary and cervix with different histopathology: A rare case report

2016 ◽  
Author(s):  
Alok Tiwari ◽  
Dhananjay Gughe ◽  
Radhika Dureja ◽  
Satinder Kaur
Keyword(s):  
Squamous Cell Carcinoma ◽  
Case Report ◽  
Cell Carcinoma ◽  
Contrast Enhancement ◽  
Squamous Cell ◽  
Pap Smear ◽  
Ca 125 ◽  
Post Contrast ◽  
Palpable Mass ◽  
Diffusion Restriction

Concurrent different histopathological types of gynecologic tumors arise rarely. We present ovarian serous and cervical squamous cell carcinoma formed synchronously. A 51-year-old woman with a poor general condition was admitted with gradual distension of abdomen for 1 year with gradual loss of weight and appetite for the last three months and pain in the abdomen and irregular vaginal bleeding for the last two months. There was no family history of malignancy of genital tract, breast or colon. On examination she was cachexic, pale, dehydrated, tachypnoeic and had edema over feet. Per abdomen examination revealed solid, non-mobile palpable mass arising from pelvis. Per vaginal examination revealed large mass in pelvis and uterus can not be felt separately on per speculum examination there was small endocervical erosion, hypertrophied cervix. On per rectal examination bilateral parametria were free. Her tumor marker were evaluated and CA-125 was found to be raised (CA 125: 915.6 u/ml U/mL); rest tumor markers were normal. Cervical punch biopsy was suggestive of moderately differentiated carcinoma and pap smear was also suggestive of cervical cancer. MRI findings revealed a mass of altered signal intensity 2.5 × 1.5 × 2.2 cm with diffusion restriction and post contrast enhancement in the anterior lip of cervix and another large, lobulated predominantly solid mass, hypo intense on T1, intermediate on T2 with diffusion restriction and post contrast enhancement in the right adnexal region abutting the small bowel and sigmoid colon optimal debulking surgery with standard protocol was done. Histopathology report revealed squamous cell carcinoma of cervix, grade III and high grade serous cystadenocarcinoma of ovary. Tumour deposits from ovary were seen on right fallopian tube and right parametrium. Squamous cell carcinoma cervix involved ectocervix, endocervix and infiltrated near full thickness of cervical stroma, endomyometrium, vaginal cuff, paracervical tissue omentum and appendix were free of tumour. Twenty five right pelvic lymphnodes dissected were free of tumour, (00/25). One out of fifteen lymphnode dissected were involved with extra capsular extent, 01/15 and thirteen para aortic lymph node dissected were free of tumor. Immunohistochemistry markers: Ovarian mass-tumour cell expressed ck, vimentin, wt-1 with focal Ck positivity, no expression of ck20, p63, ck5/6 and CEA seen. Cervical tumour-tumour cells expressed ck, ck7, p63 and ck5/6 no expression of ck20, wt-1. Based on our case report we need to keep in mind that even if patient presents with symptoms pertaining to a single malignancy; still the rare possibility of synchronous malignancies should be looked for by doing proper investigations. In our case, patient had symptoms pertaining to ovarian malignancy; whereas cervical malignancy was diagnosed after investigating the patient. Histologic examination should be done properly as the prognosis depends on the malignancies being metastatic or synchronous one appropriate management should be offered in all such cases. Long term follow up of such patients should be maintained to determine the prognosis.

scholarly journals Retroperitoneal cystic immature teratoma in an infant with post-operative chylous ascite: A case report

2021 ◽  
pp. 101823
Author(s):  
Sana Mosbahi ◽  
Sahla Sallemi ◽  
Nouha Ben Abdejelil ◽  
Salma Mani ◽  
Sabrine Ben Youssef ◽  
...  
Keyword(s):  
Case Report ◽  
Immature Teratoma

Lipoma in olecranon bursa: A case report

2021 ◽  
Vol 3 ◽  
pp. 67-69
Author(s):  
Shalini Agarwal ◽  
Jyoti Siwach ◽  
Ramneet Wadi ◽  
Nipun Gupta
Keyword(s):  
Magnetic Resonance Imaging ◽  
Case Report ◽  
Magnetic Resonance ◽  
Contrast Enhancement ◽  
Local Anesthesia ◽  
Signal Intensity ◽  
Ultrasound Examination ◽  
Fat Cells ◽  
Resonance Imaging ◽  
Diffusion Weighted Images

We report a case of a 55-year-old male patient who presented with swelling over his right elbow of 5-year duration. An ultrasound examination revealed an echogenic mass within the olecranon bursa. On magnetic resonance imaging, the mass revealed the signal intensity of fat, and it was attached to the bursal lining by means of a pedicle. There was no restriction on diffusion-weighted images and no significant contrast enhancement. Excision was performed under local anesthesia. The excised specimen revealed mature fat cells on histopathology.

scholarly journals Ovarian Yolk Sac Tumor: A Case Report with Review Of Literature

2016 ◽  
Vol 2 (1) ◽  
pp. 15-17
Author(s):  
A Sreehari ◽  
BM Rupakala
Keyword(s):  
Case Report ◽  
Early Adulthood ◽  
Germ Cell Tumors ◽  
Yolk Sac ◽  
Immature Teratoma ◽  
Yolk Sac Tumor ◽  
Histological Subtype ◽  
Review Of Literature ◽  
Yolk Sac Tumors ◽  
Ovarian Dysgerminoma

ABSTRACT A total of 3 to 5% of all ovarian malignancies include malignant ovarian germ cell tumors (MOGCTs). They are subdivided into germinomatous and non-germinomatous tumors. Common types of non-germinomatous tumors include yolk sac and immature teratoma. Ovarian yolk sac tumors (YST) are the second most frequent histological subtype of MOGCTs, after ovarian dysgerminoma. They account for 20% of MOGCTs and are frequent especially in childhood and in early adulthood. We report the case of a yolk sac tumor of the ovary in a 13yrs years old female. How to cite this article Sreehari A, Rupakala BM, Sarojamma C. Ovarian Yolk Sac Tumor: A Case Report with Review of Literature. J Med Sci 2016;2(1):15-17.

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