scholarly journals Splenic Gestation: A rare case report

2017 ◽  
Vol 6 (6) ◽  
pp. 2670
Author(s):  
Narendra Ramrao Patil ◽  
Shivaji Dadarao Birare ◽  
Apurva Ravindra Dale ◽  
Sanjay Khemlal Mahule
Keyword(s):  
Case Report ◽  
Ectopic Pregnancy ◽  
Rare Case ◽  
Exploratory Laparotomy ◽  
Final Diagnosis ◽  
Chorionic Villi ◽  
Splenic Parenchyma ◽  
Rare Case Report ◽  
Ectopic Pregnancies ◽  
Delay In Treatment

Abdominal ectopic pregnancy accounts for only 1.3% of all ectopic pregnancies and occurs when a fertilised ovum implants in an extra pelvic peritoneal location. Splenic pregnancy is one of the least common form of abdominal ectopic pregnancy. Early diagnosis is essential as delay in treatment carries significant potential for morbidity and mortality. We present a case of 22-year-old female with 6 weeks amenorrhoea and acute abdomen. Patient underwent emergency exploratory laparotomy with suspicion of ?splenic hemangioma  ?ruptured ectopic pregnancy. Splenectomy was performed. Final diagnosis was confirmed on histopathology showing chorionic villi invading the splenic parenchyma. 

Ovarian Ectopic Pregnancy: A Rare Case Report

2016 ◽  
Vol 1 (1) ◽  
pp. 23-24
Author(s):  
HK Premi ◽  
Sonika Dahiya ◽  
Shabina Khan ◽  
Sana Amrin ◽  
Sugandh Srivastava
Keyword(s):  
Case Report ◽  
Ectopic Pregnancy ◽  
Rare Case ◽  
Adnexal Mass ◽  
Emergency Laparotomy ◽  
Tubal Ectopic Pregnancy ◽  
Ovarian Pregnancy ◽  
Pain Abdomen ◽  
Rare Case Report ◽  
Ectopic Pregnancies

ABSTRACT Ovarian pregnancy is the most common type of non-tubal ectopic pregnancy. Ovarian ectopic pregnancy incidence after natural conception ranges from 1 in 2000 to 1 in 60,000 deliveries and accounts for 3% of all ectopic pregnancies. Here, we report a rare case of ruptured ectopic pregnancy. A 30 years old, G2P1+0L1 was admitted with amenorrhea of 1½ months and severe pain abdomen. Self urinary pregnancy test (UPT) was positive. Ultrasonography (USG) revealed it sided adnexal mass. Emergency laparotomy was done and a diagnosis of ovarian ectopic pregnancy was made. How to cite this article Dahiya S, Khan S, Premi HK, Amrin S, Srivastava S. Ovarian Ectopic Pregnancy: A Rare Case Report. Int J Adv Integ Med Sci 2016;1(1):23-24.

scholarly journals Ruptured Hemorrhagic Ectopic Pregnancy Implanted in the Diaphragm: A Rare Case Report and Brief Literature Review

Diagnostics ◽  
2021 ◽  
Vol 11 (12) ◽  
pp. 2342
Author(s):  
Ok Ju Kang ◽  
Ji Hye Koh ◽  
Ji Eun Yoo ◽  
So Yeon Park ◽  
Jeong-Ik Park ◽  
...  
Keyword(s):  
Case Report ◽  
Laparoscopic Surgery ◽  
Ectopic Pregnancy ◽  
Rare Case ◽  
Accurate Diagnosis ◽  
Abdominal Pregnancy ◽  
Mortality And Morbidity ◽  
Child Bearing ◽  
Rare Case Report ◽  
Ectopic Pregnancies

The mortality and morbidity rates of non-tubal ectopic pregnancies with abdominal hemorrhaging are 7–8 times higher than those of tubal pregnancies. Diaphragmatic pregnancy is a rare non-tubal ectopic form, causing acute abdominal hemoperitoneum. Here, we present a case of a primary diaphragmatic ectopic pregnancy with hemorrhage that was immediately diagnosed and successfully managed with laparoscopic surgery. Rapid and accurate diagnosis using appropriate imaging modalities is critical for improving the prognosis of a child-bearing woman with an abdominal pregnancy.

scholarly journals OVARIAN ECTOPIC PREGNANCY WITH IUCD IN SITU- A RARE CASE REPORT

2018 ◽  
Vol 7 (45) ◽  
pp. 4926-4928
Author(s):  
Shweta Gupta ◽  
Kajal Kunwar ◽  
Mukta Agrawal ◽  
Nimisha Agrawal ◽  
Ankita Mani
Keyword(s):  
Case Report ◽  
Ectopic Pregnancy ◽  
Rare Case ◽  
Rare Case Report

scholarly journals Multiple bilateral dermoid cysts with ectopic pregnancy: a rare case report

2020 ◽  
Vol 10 (1) ◽  
pp. 358
Author(s):  
Divya Agrawal
Keyword(s):  
Case Report ◽  
Ectopic Pregnancy ◽  
Dermoid Cyst ◽  
Ovulation Induction ◽  
Rare Case ◽  
Cystic Teratoma ◽  
Ovarian Neoplasm ◽  
Ovarian Stroma ◽  
Rare Case Report ◽  
History Of

Mature cystic teratoma (dermoid) is a common ovarian neoplasm but less frequently occurs bilaterally specially with ectopic pregnancy. It poses challenge in management in a young woman with history of infertility where preservation of ovarian stroma takes the priority. Here presented case of 30-year-old para 0, gravida 1 women who was diagnosed with ectopic pregnancy with history of infertility of 4 years. She underwent laparotomy where salpingectomy was done owing to tubal rupture. Dermoid cyst was removed simultaneously. When both ovaries were palpated, three more dermoids were found and taken off as well. Earlier ovulation induction was given before adhesions take upper hand and patient was pregnant in first cycle.  

scholarly journals Acquired colonic atresia in a 4-month old term male infant: a rare case report

2017 ◽  
Vol 4 (2) ◽  
pp. 669
Author(s):  
Kamal Nain Rattan ◽  
Gurupriya J. ◽  
Shruti Bansal ◽  
Rohit Kapoor ◽  
Roomi Yadav
Keyword(s):  
Case Report ◽  
Necrotizing Enterocolitis ◽  
Rare Case ◽  
Male Infant ◽  
Abdominal Distension ◽  
Exploratory Laparotomy ◽  
Inflammatory Mass ◽  
Colonic Atresia ◽  
Rare Case Report ◽  
History Of

Acquired colonic atresias are very rare but, are known in association with necrotizing enterocolitis. We report a case of a 4-month term male infant with recurrent episodes of abdominal distension, bilious vomiting and constipation off and on, without the history of necrotizing enterocolitis. Exploratory laparotomy was performed, an inflammatory mass with multiple dense interloop adhesions were found in the mid-transverse colon. These adhesions were lysed to identify the proximal dilated and distal blind end of the colon.  Rest of the gut was normal.  This case is unique for the fact that, it is a case of acquired colonic atresia without history of necrotizing enterocolitis, unlike other reported cases of acquired colonic atresia.

scholarly journals A gastric duplication cyst incidentally discovered during an obesity surgery for a 55-year-old female: a rare case report from Syria

2020 ◽  
Vol 2020 (7) ◽  
Author(s):  
Marah Mansour ◽  
Ola Souliman ◽  
Sawsan Ismail ◽  
Tamim Alsuliman ◽  
Fadi Souleiman
Keyword(s):  
Sleeve Gastrectomy ◽  
Case Report ◽  
Rare Case ◽  
Final Diagnosis ◽  
Duplication Cyst ◽  
Histopathological Study ◽  
Gi Tract ◽  
Gastric Duplication ◽  
Gastric Duplication Cyst ◽  
Rare Case Report

Abstract A gastric duplication cyst (GDC) is an uncommon gastrointestinal (GI) tract anomaly in adults. Nonspecific symptoms make it difficult to diagnose, while radiological examination might be helpful. However, the final diagnosis is made after eradication and histopathological study. Herein we report a case of an asymptomatic, incidentally diagnosed gastric duplication cyst discovered during laparoscopic sleeve gastrectomy in a 55-year-old female.

Massive hemorrhage from a unique old cesarean scar ectopic pregnancy with negative urine and serum β-HCG: a rare case report

2018 ◽  
Vol 130 (8) ◽  
pp. 708-711
Author(s):  
Xiao Yang ◽  
Xiao-Qing Wei ◽  
Dan Feng ◽  
Wei He ◽  
Yuan Chen ◽  
...  
Keyword(s):  
Case Report ◽  
Ectopic Pregnancy ◽  
Rare Case ◽  
Massive Hemorrhage ◽  
Cesarean Scar ◽  
Rare Case Report ◽  
Β Hcg ◽  
Urine And Serum

scholarly journals Endometrial stromal nodule: a rare case report

2020 ◽  
Vol 9 (5) ◽  
pp. 2170
Author(s):  
Shreya Bhattarai ◽  
Taru Gupta ◽  
Jagriti Bhardwaj ◽  
Aanchal Sablok
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Conservative Surgery ◽  
Final Diagnosis ◽  
Diagnostic Methods ◽  
Cystic Degeneration ◽  
Rare Case Report ◽  
Preoperative Diagnostic ◽  
Abdominal Route ◽  
Benign Tumours

Endometrial stromal nodules (ESN) are benign tumours of mesenchymal origin with features reminiscent of proliferative phase endometrial stroma. Diagnosis of ESNs can be established only by light microscopy and no preoperative diagnostic methods are available. Although ESNs are benign and rare, distinguishing it from other types of invasive stromal tumours is of utmost importance since prognosis and management change considerably with the diagnosis. This was a rare case report of endometrial stromal nodule in a nulliparous woman, 30 years old who presented with complaint of menorrhagia and primary infertility and had a preoperative diagnosis of large leiomyoma with cystic degeneration. She underwent a fertility preserving conservative surgery i.e. myomectomy via abdominal route, histopathology reports of which revealed endometrial stromal nodule that changed the final diagnosis and follow up regime of the patient.

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