Osteosarcoma of the Myometrium Synchronous with Bilateral Papillary Cystadenocarcinoma of the Ovary and Papillary Adenocarcinoma of the Cervix

1988 ◽  
Vol 74 (2) ◽  
pp. 227-231 ◽  
Author(s):  
Fulvio Basolo ◽  
Raffaele Pingitore ◽  
Angelo Gadducci
Keyword(s):  
Genital Tract ◽  
Rare Case ◽  
Female Genital Tract ◽  
Papillary Adenocarcinoma ◽  
Pathological Features ◽  
Primary Tumors ◽  
The World ◽  
Clinical And Pathological Features ◽  
Female Genital

We report an extremely rare case of a 60-year-old woman with myometrial osteosarcoma associated with bilateral papillary cystadenocarcinoma of the ovary and papillary adenocarcinoma of the cervix. The uterine osteosarcoma is the seventh case reported in the world, while it is the second case of syncronous triple primary tumors of the upper female genital tract. Clinical and pathological features of previously reported cases of uterine osteosarcoma and triple primary neoplasias of the upper female genital tract are critically reviewed.

scholarly journals Synchronous primary tumors of the endometrium and ovary

1970 ◽  
Vol 2 (3) ◽  
pp. 189-192 ◽  
Author(s):  
S Karki ◽  
U Chapagain
Keyword(s):  
Genital Tract ◽  
Endometrial Hyperplasia ◽  
Female Genital Tract ◽  
Premenopausal Women ◽  
Ovarian Tumors ◽  
University Teaching ◽  
Primary Tumors ◽  
Atypical Endometrial Hyperplasia ◽  
Ovarian Cancers ◽  
Female Genital

Background: Primary synchronous cancer of the female genital tract is a relatively uncommon. Simultaneously detected endometrial and ovarian malignancies constitute the commonest occurrence. A set of pathological criteria has been described to differentiate synchronous primaries from metastatic tumors. The purpose of this study was to characterize patients with synchronous primary endometrial and ovarian tumors. Materials and Methods: This was a retrospective study done in Department of Pathology, Tribhuwan University Teaching Hospital from September 2006 to August 2011. The datas were retrieved from computer database. Results: There were totally of 10 cases of simultaneously detected endometrial and ovarian cancers. Out of 10 cases, 7 cases were synchronous primary endometrial and ovarian cancers while three were metastatic. Median age at presentation was 47.4 years. Six (85.8%) of these patients presenting with dual primary tumors were premenopausal. Grade 1 histology was seen in 57% of endometrial and 42% of ovarian tumors. Atypical endometrial hyperplasia was found in 42.8% of cases while none of the cases showed endometriosis. Conclusion: Though limited by relatively small number of cases, younger and premenopausal women were predisposed to developing synchronous primary tumors of the endometrium and ovary. DOI: http://dx.doi.org/10.3126/jpn.v2i3.6019 JPN 2012; 2(3): 189-192

scholarly journals Synchronous primary ovarian sex cord tumor and endometrial cancer

2016 ◽  
Author(s):  
S. A. Iqbal ◽  
H. Shukla ◽  
V. Jain ◽  
S. Giri ◽  
R. Sekhon ◽  
...  
Keyword(s):  
Genital Tract ◽  
Ovarian Tumor ◽  
Early Stage ◽  
Female Genital Tract ◽  
Low Grade ◽  
Primary Tumors ◽  
Stromal Tumors ◽  
Gynaecological Tumours ◽  
Sex Cord Stromal Tumors ◽  
Female Genital

Synchronous primary tumors of female genital tract are rare with a rate of about 0.7-1.8% of all gynaecological tumours. Most common primary tumours presenting as synchronous lesions are ovary and endometrium. However, sex cord stromal tumors are rare variety of primary ovarian tumor and synchronous with endometrium is even much rarer. These tumors are detected usually in younger, overweight, nulliparous and perimenopausal female. Synchronous primary tumors of endometrium and ovary have a better prognosis than the either of above alone because these are usually low grade and diagnosed at early stage. We present a report of four cases of synchronous endometrial and sex cord stromal tumors of ovary.

scholarly journals Treated with Hymen Sparing Surgery in Familial Imperforate Hymen

2021 ◽  
Vol 3 (5) ◽  
pp. 12-14
Author(s):  
M. Kaplanoglu
Keyword(s):  
Genital Tract ◽  
Rare Case ◽  
Chronic Pelvic Pain ◽  
Female Genital Tract ◽  
Pelvic Mass ◽  
Rare Condition ◽  
Familial Occurrence ◽  
Imperforate Hymen ◽  
Family Culture ◽  
Female Genital

Imperforate hymen is a rare congenital female genital tract obstructive pathology. Although It is generally sporadic and isolated, very rare familial occurrence cases have been published in the literature. We present a rare case of the familial occurrence of IH and its surgical treatment. This case was admitted to our clinic with chronic pelvic pain, difficulty urination and pelvic mass. After the gynecologic examination and ultrasound view, the diagnosis of IH was made.  Her sister who two years older than she had been previously evaluated for amenorrhea and her sister had undergone surgical procedures for IH. Because of Hymen is an important symbol of virginity in family culture, hymen sparing surgery was performed. The familial occurrence of IH is a rare condition and very few reported cases in the literature. Hymenectomy can cause social retraction in cases therefore hymen sparing surgery is an important surgery, especially Muslim cultures.

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 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.

Synchronous primary tumors of the female genital tract: a single center experience

2008 ◽  
Vol 279 (5) ◽  
pp. 667-672 ◽  
Author(s):  
Tayfun Gungor ◽  
Mine Kanat-Pektas ◽  
Emin Ustunyurt ◽  
Leyla Mollamahmutoglu
Keyword(s):  
Genital Tract ◽  
Female Genital Tract ◽  
Single Center ◽  
Primary Tumors ◽  
Single Center Experience ◽  
Female Genital

scholarly journals Extramedullary Leukemia, Presenting at the Cervix of the Uterus

2020 ◽  
Vol 2020 ◽  
pp. 1-13
Author(s):  
Nikolaos Tsagkas ◽  
Androniki Troussa ◽  
George Vorgias ◽  
Olympia Tzaida ◽  
Nektaria Zagorianakou ◽  
...  
Keyword(s):  
Genital Tract ◽  
Rare Case ◽  
Survival Rates ◽  
Female Genital Tract ◽  
Lymphocytic Leukemia ◽  
Pap Smears ◽  
Microscopic Evaluation ◽  
Extramedullary Relapse ◽  
Leukemia Relapse ◽  
Female Genital

Extramedullary relapse of leukemia is encountered more often than in the past. The reason is that leukemia survival rates increase with improved treatment schemes. We present a rare case of involvement of the cervix of the uterus in an adult B Acute Lymphocytic Leukemia (B-ALL) survivor. Relapses affect various organs but rarely the female genital tract. Nevertheless, in this case, a woman with a history of induced amenorrhea due to treatment for leukemia presented to the gynecologist because of vaginal spotting. Colposcopy evaluation of the vagina/cervix, sonography and cytological and histological sampling established the diagnosis of leukemia relapse in the cervix of the uterus. Under these circumstances, our study highlights the rare extramedullary presentation of leukemia in the cervix of the uterus of a young lady considered to be disease-free and listed for bone marrow transplantation. In this rare case of relapse in the cervix of the uterus, Pap smears alarmed physicians, and radiology examinations assisted the diagnostic workup. Still, only biopsy, microscopic evaluation, and immunohistochemistry studies established the exact diagnosis. Prognosis in the situation of extramedullary disease relapse in the female genital tract was poor, but gynecologists’ high suspicion led to a prompt diagnosis. Survival is in general limited, but together with high suspicion, multidisciplinary team involvement is imperative to improve the reduced chances of survival.

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