scholarly journals Triple Synchronous Primary Neoplasms of the Cervix, Endometrium, and Ovary: A Rare Case Report and Summary of All the English PubMed-Indexed Literature

2017 ◽  
Vol 2017 ◽  
pp. 1-6 ◽  
Author(s):  
Ahmed Abu-Zaid ◽  
Mohannad Alsabban ◽  
Mohammed Abuzaid ◽  
Osama Alomar ◽  
Hany Salem ◽  
...  
Keyword(s):  
Case Report ◽  
Rare Case ◽  
Single Case ◽  
English Literature ◽  
Genital System ◽  
Summary Table ◽  
Female Genital System ◽  
Rare Case Report ◽  
Primary Neoplasms ◽  
Female Genital

The incidence rate of triple or more synchronous primary neoplasms of the female genital system is exceedingly uncommon. To the best of our knowledge, only 13 such cases have been reported in the PubMed-indexed English literature. Herein, we report a single case of triple synchronous primary neoplasms of the cervix, endometrium, and left ovary with three distinct histological patterns that were not reported previously. Moreover, we briefly present a summary table of all the English PubMed-indexed cases of triple or more synchronous primary neoplasms of the female genital system (n=13).

Neurofibroma of Soft Palate: A Rare Case Report

2013 ◽  
Vol 5 (2) ◽  
pp. 19-20
Author(s):  
SG Smitha ◽  
Smitha Soubhagya Gangaraj ◽  
Lakshmi Shantharam ◽  
Suguna Vijay
Keyword(s):  
Case Report ◽  
Soft Palate ◽  
Rare Case ◽  
Histopathological Examination ◽  
English Literature ◽  
Rare Tumor ◽  
Fourth Case ◽  
Intraoral Approach ◽  
Rare Case Report

ABSTRACT Neurofibroma of soft palate is a rare tumor with this report being the fourth case reported in English literature. We are reporting this case of isolated neurofibroma of soft palate for its rarity. The mass was excised by intraoral approach without prior tracheostomy. Histopathological examination showed features of neurofibroma with secondary changes.

Localized neurofibromatosis of the female genital system: A case report and review of the literature

2012 ◽  
Vol 38 (6) ◽  
pp. 953-956 ◽  
Author(s):  
Ana M. Gómez-Laencina ◽  
Francisco Martínez Díaz ◽  
Blanca Izquierdo Sanjuanes ◽  
Elena M. Vicente Sánchez ◽  
Rosario Fernandez Salmerón ◽  
...  
Keyword(s):  
Case Report ◽  
Genital System ◽  
Review Of The Literature ◽  
System A ◽  
Female Genital System ◽  
Female Genital

scholarly journals Congenital absence of a part of the fallopian tube: a case report

2016 ◽  
Vol 6 (1) ◽  
pp. 320
Author(s):  
Mukta Agarwal ◽  
Hemali H. Sinha ◽  
. Anamika
Keyword(s):  
Case Report ◽  
Fallopian Tube ◽  
Genital Tract ◽  
Rare Case ◽  
Case Reports ◽  
Female Genital Tract ◽  
Fallopian Tubes ◽  
Rare Occurrence ◽  
Rare Case Report ◽  
Female Genital

Congenital malformations of female genital tract are frequently seen in Gynaecological clinics, incidence being upto 5-6% in cases of infertility. Most of these anomalies are related to uterus and vagina, abnormalities related to ovaries and fallopian tubes are of rare occurrence and the exact incidence of these anomalies are not known, only a few incidental case reports are available in literature. Here, we present a rare case report of absent mid- tubal segment of fallopian tube in a patient of infertility.

scholarly journals Bilateral Primary Aneurysmal Bone Cyst of Proximal Femur: A Rare Case Report

2021 ◽  
pp. 217-223
Author(s):  
Sudhir Shyam Kushwaha ◽  
Kumar Shantanu ◽  
Garima Maurya ◽  
Abhishek Pandey
Keyword(s):  
Case Report ◽  
Proximal Femur ◽  
Rare Case ◽  
Pathological Fracture ◽  
English Literature ◽  
Bone Cyst ◽  
Open Biopsy ◽  
Rare Case Report ◽  
Aneurysmal Bone Cysts ◽  
The Right

Aneurysmal bone cysts (ABC) are blood-filled, locally destructive, expansile lesions of the bone. ABC of the proximal femur is usually unilateral in presentation. As far as the English literature is concerned, there is no case report of bilateral involvement of the proximal femur by primary ABC. We hereby present a rare case of bilateral primary ABC of the proximal femur with pathological fracture of the right femoral neck. The patient underwent right hip hemiarthroplasty and open biopsy and curettage of the left proximal femur. ABC is usually unilateral in location. Whenever there is a bilateral lesion in the proximal femur usually ABC is not suspected as a differential diagnosis, but ABC may have a bilateral presentation.

scholarly journals Female Hypospadias and Congenital Uterine Müllerian Anomaly with Proved Fertility: A Rare Case Report

2011 ◽  
Vol 3 (3) ◽  
pp. 155-156
Author(s):  
Rekha Choudhary ◽  
Suniti Verma ◽  
Gautam Ram Choudhary
Keyword(s):  
Case Report ◽  
Genital Tract ◽  
Rare Case ◽  
Female Genital Tract ◽  
Urogenital Sinus ◽  
Developmental Relationship ◽  
Rare Case Report ◽  
Mullerian Anomaly ◽  
Primigravid Woman ◽  
Female Genital

ABSTRACT Congenital anomalies of the female genital tract result from müllerian duct anomalies and/or abnormalities of the urogenital sinus or cloaca. Due to the close developmental relationship between the genital and the urinary tracts, association of anomalies in both systems are common. This article reviews the appearance of developmental anomalies of the female urinary (hypospadias) and genital tracts and points out complication associated with bicornuate uterus. A 40-year-old primigravid woman conceived a pregnancy after 10 years of primary infertility. The prenatal course was uncomplicated. At 38 weeks’ gestation, she was successfully delivered by elective low transverse cesarean section.

scholarly journals Epiglottic dermoid cyst: a rare case report

2021 ◽  
Vol 7 (8) ◽  
pp. 1381
Author(s):  
Ramchandra . ◽  
C. B. Nandyal ◽  
Kiran Deshmukh
Keyword(s):  
Case Report ◽  
Dermoid Cyst ◽  
Rare Case ◽  
English Literature ◽  
Age Groups ◽  
Neck Region ◽  
Surgical Excision ◽  
Complete Surgical Excision ◽  
Body Sensation ◽  
Rare Case Report

<p>Epiglottis dermoid cysts are generally benign lesions, which can affect all the age groups. Dermoid cysts arising from the head and neck region are rare, slow growing, and well-circumscribed neoplasm. Symptoms are non-specific and usually related to the size and the location of the lesion. A dermoid cyst of the epiglottis is extremely rare. To the best of our knowledge, only one case has been previously reported in the English literature and a total of three cases were presented in Russian literature in two studies. In our report, a middle-aged male presented with foreign body sensation in throat for 1-year and difficulty in swallowing for three months, mainly for solids. Thorough history, clinical examination and relevant investigation were done. Direct laryngoscopy was done and complete surgical excision was done. The aim of the case report is to present a rare case of epiglottic dermoid cyst, its clinical presentation, radio-logical features and surgical management.</p>

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