Primary Leiomyoma of ovary – A rare case report presenting with clinical diagnosis of subserosal uterine fibroid

2021 ◽  
Vol 6 (2) ◽  
pp. 144-147
Author(s):  
Ruchica Goel ◽  
Shipra Gupta ◽  
Jai Kishan Goel ◽  
Ruchee Khandelwal ◽  
Neeraj Prajapati

Primary leiomyoma of ovary are rare benign ovarian tumors. We present a rare case report of ovarian leiomyoma who was planned for laparotomy with a clinical diagnosis of subserosal uterine fibroid. Twenty three years old unmarried girl presented with heaviness and mass in lower abdomen, gravid uterus size of 20 weeks. Abdominal Ultrasonography raised suspicion of subserous fibroid. MRI pelvis was suggestive of ovarian neoplasm versus broad ligament fibroid. On laparotomy and removal of mass, histopathology and immunohistochemistry confirmed leiomyoma of ovary. Presently she is on follow up without any complaints. Ovarian leiomyoma is clinically often misdiagnosed and should be kept in differential diagnosis in lower abdominal masses.

2012 ◽  
Vol 64 (1) ◽  
pp. 70-72 ◽  
Author(s):  
Navjot Kaur ◽  
Rajni Kaushik ◽  
Anchana Gulati ◽  
Vijay Kaushal ◽  
Rubi Bindra

2020 ◽  
Vol 11 (S1) ◽  
pp. 96-101
Author(s):  
Sumit Kumar ◽  
Prashanth Giridhar ◽  
Shalini Verma ◽  
Ravi Hari Phulware ◽  
Neena Malhotra ◽  
...  

2020 ◽  
Vol 33 (2) ◽  
pp. 164-166
Author(s):  
Maruf Siddiqui ◽  
Nusrat Ghafoor ◽  
Fahmida Naznine ◽  
Rusmila Shamim Abdullah ◽  
T A Chowdhury

Broad ligament pregnancy is a rare obstetric condition. Its diagnosis is quite difficult andmanagement is challenging. Here we report a case of a 26 years old primi gravida conceivedfollowing laparoscopy and ovulation induction. Diagnosis of the broad ligament pregnancywas done by a transvaginal ultrasound at her 9 weeks and was proceded with laparoscopyfollowed by laparotomy. A right broad ligament pregnancy was found and the sac with fetuswas removed. Laparoscopy was converted into a laparotomy as there was an uncontrollablebleeding from the broad ligament. Here we present a case of this extreme rare type of broadligament pregnancy. Bangladesh J Obstet Gynaecol, 2018; Vol. 33(2) : 164-166


2016 ◽  
Vol 14 (4) ◽  
Author(s):  
Dalia Rafat ◽  
Imam Bano ◽  
Seema Hakim ◽  
Shaheen Anjum ◽  
Hena A. Ansari ◽  
...  

Author(s):  
Krishna Mandade ◽  
Kashika Singh ◽  
Aptulkar ◽  
Angarkar ◽  
DP Bhavthankar

2020 ◽  
Vol 7 (7) ◽  
pp. C91-93
Author(s):  
Ayesha Khatoon ◽  
Vyshnavi Vasantham ◽  
Urvashi Sharma ◽  
Shakti Kumar Yadav ◽  
Rupinder Kalra ◽  
...  

Ano-rectal melanoma is extremely rare and has dismal prognosis when compared to cutaneous melanomas. It presents as ano-rectal mass and patients usually complain of passing blood in stools. Being, a highly aggressive neoplasm, widespread metastasis is common, which can be seen even at the time of diagnosis. Here, we present a case report of ano-rectal melanoma in a 40-year old male, who presented with complaints of anal growth since one month. Initially, a clinical diagnosis of rectal carcinoma was suspected. However, biopsy of the growth showed histomorphological features of melanoma, which were confirmed on immunohistochemistry.


2016 ◽  
Vol 5 (36) ◽  
pp. 2171-2172
Author(s):  
Neetu Purwar ◽  
Shobha Dwivedi ◽  
Brijendra Nath Tripathi

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