scholarly journals Labial Adhesion in Adult Female

2015 ◽  
Vol 7 (3) ◽  
pp. 207-209
Author(s):  
Seetesh Ghose ◽  
P Pallavee ◽  
Jasmina Begum ◽  
Lopamudra B John ◽  
Sunil Kumar Samal
Keyword(s):  
South Asian ◽  
Adult Female ◽  
Female Genital Tract ◽  
Menstrual Blood ◽  
Normal Female ◽  
Radiological Investigation ◽  
Labia Minora ◽  
Secondary Sex Characters ◽  
Labial Adhesion ◽  
Female Genital

ABSTRACT A 23 years old female presented to gynecological outpatient department (OPD) with complain of passing urine and menstrual blood through a single small opening for 5 years. On examination, she had well developed secondary sex characters but fused labia minora with a single pinpoint opening through which she was passing both urine and menstrual blood. Radiological investigation revealed normal female genital tract. So, the case was diagnosed as labial fusion and surgically treated as medical management failed. How to cite this article Ghose S, Pallavee P, Begum J, John LB, Samal SK. Labial Adhesion in Adult Female. J South Asian Feder Obst Gynae 2015;7(3):207-209.

scholarly journals Acute abdomen in a patient with Mayer-Rokitansky-Kuster-Hauser syndrome

2008 ◽  
Vol 65 (9) ◽  
pp. 706-709 ◽  
Author(s):  
Aleksandra Petric ◽  
Milan Stefanovic ◽  
Predrag Vukomanovic ◽  
Radomir Zivadinovic ◽  
Aleksandra Tubic ◽  
...  
Keyword(s):  
Acute Abdomen ◽  
Genital Tract ◽  
Female Genital Tract ◽  
Careful Examination ◽  
Normal Female ◽  
Vascular Leiomyoma ◽  
Primary Amenorrhoea ◽  
Healthy Women ◽  
Dead End ◽  
Female Genital

Background. Mayer-Rokitansky-Kuster-Hauser (MRKH) syndrome is a malformation of female genital tract (incidence 1 in 4000 female newborn children). It appears as a result of a disorder in the development of Millerian cannals. Etiology is unknown. Syndrome MRKH is the most frequent cause of primary amenorrhoea (90%). Patients with MRKH have a normal female phenotype, with normal pubic hairness and thelarche, and female karyotype (46XX) followed by primary amenorrhoea. Hormonal status corresponds to healthy women, where the appearance of ovarian tumors and tumors on rudiment parts of uterus is possible. Case report. We presented a case of acute abdomen in a patient with previously not diagnosed MRKH. The diagnosis was done during the operation. Small pelvis and an abdominal part were filled with torquated tumor lump, where ovaries, oviducts, uterus or something resembling rudiment of uterus were not recognized through careful examination. Furthemore, the patient had a short, dead-end vagina. Tumorectomy was done and hystopathological finding showed the presence of vascular leiomyoma. Conclusion. The diagnosis of complex syndromes, such as MRKH, can, despite modern diagnostics, be absent for non-medical and psycho-social reasons. We can expect ovarian and uterine pathology on hypoplastic structures in these patients, as well as in healthy women. Vascular leiomyoma in the patients with MRKH was not found in the available literature.

scholarly journals Imperforate Hymen

2014 ◽  
Vol 2 (1) ◽  
pp. 52-53
Author(s):  
Krishna Dahiya ◽  
Pushpa Dahiya ◽  
Shaveta Jain ◽  
Nupur LNU
Keyword(s):  
South Asian ◽  
Adolescent Girls ◽  
Female Genital Tract ◽  
Lower Abdominal Pain ◽  
Conclusive Evidence ◽  
Imperforate Hymen ◽  
Delay In Diagnosis ◽  
Presenting Symptoms ◽  
Proper Diagnosis ◽  
Female Genital

ABSTRACT Imperforate hymen is relatively rare but it is the most frequently encountered of the mulleriananomalies of the female genital tract with an incidence of about 0.1%. The clinical presentation varies significantly from patient to patient depending on the age at diagnosis but in most cases, the diagnosis is missed in early childhood delaying the diagnosis upto puberty, when the patient presents with hematocolpos, hematometra or both. When this happens, the presentation could even be misleading because of unlikely presenting symptoms like, urinary retention and bowel obstruction leading to unnecessary urology and gastroenterology referral without any conclusive evidence of the condition furthering the delay in diagnosis and increasing the presentation with complications. This case is an illustration that there is quite often a considerable delay before a proper diagnosis is reached. The aim of this communication is to increase awareness of imperforate hymen among clinicians examining adolescent girls with lower abdominal pain. How to cite this article Dahiya P, Dahiya K, Jain S, Nupur. Imperforate Hymen. J South Asian Feder Menopause Soc 2014;2(1):52-53.

scholarly journals Krukenberg Tumor in Adolescent: A Rare Occurrence

2014 ◽  
Vol 6 (3) ◽  
pp. 202-204
Author(s):  
G Nandini ◽  
K Umadevi ◽  
K Padma ◽  
Rajini Uday
Keyword(s):  
South Asian ◽  
Genital Tract ◽  
Adolescent Girl ◽  
Female Genital Tract ◽  
Histopathological Diagnosis ◽  
Krukenberg Tumor ◽  
Ovarian Malignancy ◽  
Rare Occurrence ◽  
Krukenberg Tumors ◽  
Female Genital

ABSTRACT Krukenberg tumors classically refer to secondary ovarian malignancy. The primary is mostly from female genital tract, breast and gastrointestinal tract. Krukenberg tumors account for 30 to 40% of metastatic cancers to the ovaries. The average age of occurrence is 45 years. Most of the Krukenberg tumors are histopathological diagnosis done postoperatively. We do report a case of Krukenberg tumor in an adolescent girl. How to cite this article Nandini G, Umadevi K, Padma K, Uday R. Krukenberg Tumor in Adolescent: A Rare Occurrence. J South Asian Feder Obst Gynae 2014;6(3):202-204.

scholarly journals A Rare Clinical Presentation of Giant Bilateral Labial Fibroepithelial Stromal Polyps in Patient with Psoriasis Disease

2016 ◽  
Vol 2016 ◽  
pp. 1-3
Author(s):  
Ayse Filiz Avsar ◽  
Elcin Islek ◽  
Melahat Yildirim ◽  
Hilal Ahsen
Keyword(s):  
Genital Tract ◽  
Clinical Presentation ◽  
Female Genital Tract ◽  
Labia Minora ◽  
Fibroepithelial Polyps ◽  
Left And Right ◽  
Reproductive Aged Women ◽  
Female Genital

Fibroepithelial polyps (FEPs) are rarely seen lesions of the lower female genital tract with polypoid proliferations of stroma. These tumors usually present in the vulvovaginal region of the reproductive aged women. In this presentation, we report a case of a psoriatic woman who developed unusual multiple polypoid lesions approximately 15 cm in size arising from both left and right labia minora and unique connection of FEPs with psoriasis disease.

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