scholarly journals A Rare Case of Cervical Fibroid in a Young Woman Managed by Uterus Conserving Surgery

Author(s):  
Chandana Galidevara ◽  
Dhivya Rajarajan

Cervical fibroid is a surgical challenge to the gynaecologist, more so when an attempt to conserve the uterus is made in young patients who want to preserve their fertility. The presenting complaint in cervical fibroids are mainly pressure symptoms due to compression on surrounding structures in the pelvis, which is an indication for surgical management. The mainstay of treatment in older patients who have completed family has been hysterectomy. Here authors report a case of 29-year-old young multiparous women, who underwent caesarean section in her second pregnancy because of cervical fibroid diagnosed antenatally elsewhere, presented to us postnatally with pain and pressure symptoms with abdominal distension due to that central cervical fibroid for 7 months in the postnatal period. She was managed by uterus conserving surgery with the involvement of a multi-disciplinary team.

Author(s):  
Rupali Rautela ◽  
Rahul Katiyar ◽  
Nitish Kharayat ◽  
Abhishek Kumar ◽  
Deepesh Gautam ◽  
...  

A non-descript doe was presented with the complaint of excessive bilateral abdominal distension and with unknown breeding history. Ultrasound examination revealed excessive anechoic area in uterus along with two fetuses. On caesarean section, dropsy of amnion was observed and one normal fetus co-twin with “bulldog” anasarcous fetus was removed.


2021 ◽  
Vol 28 (2) ◽  
pp. E202126
Author(s):  
Sanae Sninate ◽  
Habib Bellamlih ◽  
Soukaina Allioui ◽  
Leila Jroundi ◽  
Fatima Zahrae Laamrani

Background. Ogilvie syndrome is a rare postpartum complication. It is characterized by an acute colonic pseudo-obstruction which occurs in the absence of a mechanical cause. Early detection of the diagnosis is essential to avoid cecal perforation. Case report. We report a case of Ogilvie syndrome following caesarean section in a 39-year-old woman (gravida 2, para 2) with a history of secondary infertility 10 years ago due to tubal stenosis and subserous fibroma, which led to the indication for cesarean section in second pregnancy at 39 weeks of gestation. Three days after cesarean section, the patient presented with significant abdominal distension and tenderness, vomiting, weakness, and nausea; an abdominal X-ray showed cecal distension. Abdominal computed tomography scan with intravenous contrast revealed distension of the ascending and transverse colon with air-fluid levels but without transitional mechanical obstruction. The patient was successfully treated. Conclusions. Ogilvie syndrome is a rare but serious complication that should be considered in fit young patients who present with pain, severe abdominal distension and failure to pass flatus after caesarean section.


2020 ◽  
Vol 14 (3) ◽  
pp. 84-86
Author(s):  
Rmana Bai Ramavath ◽  
◽  
DantamHymavathi Devi ◽  

2019 ◽  
Vol 21 (10) ◽  
pp. 798-800 ◽  
Author(s):  
Zhijun Zhang ◽  
Qinghong Ke ◽  
Weiliang Xia ◽  
Xiuming Zhang ◽  
Yan Shen ◽  
...  

Background: Hemolymphangioma is a rare benign tumor. To the best of our knowledge, there were only 10 reports of this tumor of the pancreas until March 2018. Case Report: Here, we reported a large invasive hemolymphangioma of the pancreas in a young woman with a complaint of abdominal distension and an epigastric mass about 3 weeks. She was found to have a huge multilocular cystic tumor at the neck and body of pancreas on computed tomography. She was eventually diagnosed with hemolymphangioma of the pancreas after operation. After 2 years of follow-up, there was no signs of recurrence. Conclusion: From our case and literature, we can conclude that hemolymphangioma of the pancreas is uncommon benign tumor, and it is hard to make an accurate diagnosis preoperatively. Radical surgical resection should be performed whenever possible. The prognosis of this disease seems good.


2021 ◽  
Author(s):  
Miriam Veleno ◽  
Ettore Maggio ◽  
Cesare Morgante ◽  
Roberto Novizio ◽  
Leo Maria Laura ◽  
...  

2018 ◽  
Vol 16 (2) ◽  
Author(s):  
Sangeeta Pankaj ◽  
Anjili Kumari ◽  
Syed Nazneen ◽  
Jaya Kumari ◽  
Vijayanand Choudhary ◽  
...  

2011 ◽  
Vol 25 (1) ◽  
pp. 17
Author(s):  
Xiao Luo ◽  
Li Xiao Wan ◽  
Hong Shen ◽  
Yin Xiu Xia ◽  
Chao Han Zhang ◽  
...  

<em>Objective</em>. Treatment of anterior vaginal wall prolapse and stress urinary incontinence (SUI) with transobturator tension-free vaginal mesh (anterior Prolift) and concomitant tension-free vaginal tape-obturator (TVT-O) has been proved feasible, safe and effective. However, there is little known about the influence of pregnancy on women who have had such procedures before pregnancy. <em>Design and methods.</em> A 32-year-old woman (gravid 1, para 1) with two years history of SUI and nine months history of pelvic organ prolapse (POP) was treated with transobturator tension-free vaginal mesh (anterior Prolift) and concomitant TVT-O. Her recovery was excellent, and she was pregnant eight months after the operation. <em>Results</em>. The patient went through her pregnancy smoothly with no special discomfort and successfully delivered an infant via caesarean section without recurrence of POP and SUI. Her last visit to our clinic about 14 months after caesarean section revealed that the anterior Prolift mesh and TVT-O mesh still remained intact and the position of the vaginal fornix, anterior and posterior walls and uterus also remained normal. <em>Conclusions</em>: Pelvic floor reconstruction with vaginal mesh (Prolift) may have positive significance for young patients who desire uterine preservation for future pregnancies. However, further studies are warranted to determine whether it can be used in pregnant women or women planning future pregnancies.


2015 ◽  
Vol 19 (4) ◽  
pp. 154 ◽  
Author(s):  
Ji Soo Lee ◽  
Jong Man Kim ◽  
Seunghwan Lee ◽  
Jin-Yong Choi ◽  
Wontae Cho ◽  
...  

2021 ◽  
Vol 11 (6) ◽  
pp. 197-199
Author(s):  
Challa Sravani ◽  
Madhura M Killedar

Isolated cecal necrosis is a rare abdominal condition. Usually presents as acute appendicitis clinically. Mostly occurring in older patients with cardiac and renal comorbidities. Anatomical abnormality of cecal blood supply is usually observed. Diagnosis is difficult preoperatively without high degree of suspicion. Any delay in diagnosis can lead to fatal complication. Key words: isolated cecal necrosis, ischemic colitis, acute appendicitis.


Author(s):  
Yusrawati Yusrawati ◽  
Reno Muhatiah

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


Sign in / Sign up

Export Citation Format

Share Document