Female Adnexal Tumour of Wolffian Origin Masquerading as a Broad Ligament Fibroid: A Rare Case Report

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

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Vascular Hamartoma of Broad Ligament: A Rare Case Report

Indian Journal of Gynecologic Oncology ◽

10.1007/s40944-016-0081-1 ◽

2016 ◽

Vol 14 (4) ◽

Author(s):

Dalia Rafat ◽

Imam Bano ◽

Seema Hakim ◽

Shaheen Anjum ◽

Hena A. Ansari ◽

...

Keyword(s):

Case Report ◽

Rare Case ◽

Broad Ligament ◽

Rare Case Report ◽

Vascular Hamartoma

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

IP Journal of Diagnostic Pathology and Oncology ◽

10.18231/j.jdpo.2021.031 ◽

2021 ◽

Vol 6 (2) ◽

pp. 144-147

Author(s):

Ruchica Goel ◽

Shipra Gupta ◽

Jai Kishan Goel ◽

Ruchee Khandelwal ◽

Neeraj Prajapati

Keyword(s):

Case Report ◽

Clinical Diagnosis ◽

Uterine Fibroid ◽

Rare Case ◽

Broad Ligament ◽

Gravid Uterus ◽

Abdominal Ultrasonography ◽

Abdominal Masses ◽

Rare Case Report ◽

Benign Ovarian Tumors

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.

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Aggressive angiomyxoma presenting as huge broad ligament tumor-A rare case report

International Journal of Medical Research & Health Sciences ◽

10.5958/j.2319-5886.3.1.038 ◽

2014 ◽

Vol 3 (1) ◽

pp. 186

Author(s):

Krishna Mandade ◽

Kashika Singh ◽

Aptulkar ◽

Angarkar ◽

DP Bhavthankar

Keyword(s):

Case Report ◽

Rare Case ◽

Broad Ligament ◽

Aggressive Angiomyxoma ◽

Rare Case Report

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Female Adnexal Tumour of Wolffian Origin: A Rare Case Report

JOURNAL FOR CLINICAL AND DIAGNOSTIC RESEARCH ◽

10.7860/jcdr/2021/48880.15108 ◽

2021 ◽

Author(s):

Soumit Dey ◽

Pritam Ray ◽

Debasish Bhattacharya ◽

Mrinal Kanti Chaudhuri ◽

Subir Kumar Dutta

Keyword(s):

Fallopian Tube ◽

Rare Case ◽

Histopathological Examination ◽

Broad Ligament ◽

Histopathological Diagnosis ◽

Rare Tumour ◽

Rare Case Report ◽

Mesonephric Duct ◽

Cellular Pleomorphism ◽

Adnexal Tumour

Female Adnexal Tumour of Wolffian Origin (FATWO) is a rare tumour occurring in adnexal region, arising from the remnants of the mesonephric duct, in places like the broad ligament, fallopian tube, ovarian hilum, peritoneum. Here the authors have reported a case of FATWO in a 47-year-old woman occurring in the wall of fallopian tube and confirmed with immunohistochemistry. Most of these tumours behave in a benign fashion but certain histological features like hypercellularity, cellular pleomorphism and nuclear atypia cause significant confusion in histopathological diagnosis. Multiple differential diagnoses were considered. After careful histopathological examination and thorough investigation with multiple immunohistochemical stains, the diagnosis was ultimately established.

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