scholarly journals SAT-494 A Very Rare Case: Hypercalcemia Caused by Ectopic PTH Secretion in Endometrial Cancer

2019 ◽  
Vol 3 (Supplement_1) ◽  
Author(s):  
Nour Batarseh ◽  
Farah Al Sabie ◽  
Carmella Evans-Molina
Keyword(s):  
Endometrial Cancer ◽  
Rare Case

scholarly journals The co-occurrence of leukemoid reaction and hypercalcemia in a patient with endometrial cancer: A case report and literature review

2021 ◽  
Vol 104 (2) ◽  
pp. 003685042110040
Author(s):  
Weimin Tao ◽  
Qin Yan ◽  
Yao Zhou ◽  
Yanli Wang ◽  
Zhiqiang Liu ◽  
...  
Keyword(s):  
Endometrial Cancer ◽  
Early Identification ◽  
Metabolic Alkalosis ◽  
Rare Case ◽  
Symptomatic Treatment ◽  
Clinical Situation ◽  
Paraneoplastic Syndromes ◽  
Leukemoid Reaction ◽  
Clinical Prognosis ◽  
Infection Treatment

Paraneoplastic syndromes are rarely seen in gynecological tumors especially in endometrial cancer. Early identification of paraneoplastic syndromes plays a significant role in the treatment and prognosis of cancer. Here, we reported a rare case with endometrial cancer with a 2.7 cm × 2.2 cm × 3.4 cm lesion in the posterior cervix presenting leukemoid reaction and hypercalcemia as paraneoplastic syndromes simultaneously. During the progress of the endometrial cancer, her leukocyte level rose up to 60.7 × 109/L after anti-infection treatment. Meanwhile, the patient represented a series of severe clinical situation including hypercalcemia, hypokalemia, metabolic alkalosis. and respiratory failure. Finally, the patient died of respiratory circulatory failure 2 weeks later. In addition to symptomatic treatment, possible treatment targeted on the primary tumor as early as possible might help to improve the clinical prognosis.

scholarly journals Persistent genital arousal disorder: always look beyond the surface - a case report

2021 ◽  
Vol 10 (4) ◽  
pp. 1691
Author(s):  
Rita Sarabando ◽  
Natacha Sousa ◽  
Ana C. Borges ◽  
Cristina Nogueira-Silva
Keyword(s):  
Endometrial Cancer ◽  
Rare Case ◽  
Case Reports ◽  
Rare Condition ◽  
Specific Context ◽  
Comprehensive Review ◽  
Genital Arousal ◽  
Arousal Disorder ◽  
Multiple Diagnosis

Persistent genital arousal disorder is a rare condition characterized by unwanted intrusive symptoms of sexual arousal without specific context. Their possible aetiologies and treatments are multiple and mostly based on case reports. We aim to do a comprehensive review of persistent genital arousal disorder and describe a case of a postmenopausal woman who developed this disease and, during the follow-up, was diagnosed with advanced endometrial cancer, reminding physicians to keep in mind the possibility of multiple diagnosis in the same patient, including malignancy. Although there is no description of this association in the literature, the possible aetiologies of persistent genital arousal disorder are diverse, and we sought this rare case should be disclosed.

Bilateral Mature Cystic Teratomas of the Ovary with Endometrial Cancer: A Rare Case Presentation

2017 ◽  
Vol 33 (3) ◽  
pp. 126-128
Author(s):  
Krishna Dahiya ◽  
Kriti Agarwal ◽  
Savita Singhal
Keyword(s):  
Endometrial Cancer ◽  
Rare Case ◽  
Case Presentation

Rare case of stage IA epithelial ovarian cancer with bone as the first site of recurrent metastasis

2006 ◽  
Vol 16 (Suppl 1) ◽  
pp. 322-326 ◽  
Author(s):  
K.-H. Chang ◽  
J.-P. Lee ◽  
H.-S. Ryu
Keyword(s):  
Ovarian Cancer ◽  
Cervical Cancer ◽  
Endometrial Cancer ◽  
Epithelial Ovarian Cancer ◽  
Poor Prognosis ◽  
Rare Case ◽  
Advanced Disease ◽  
Early Stage ◽  
Good Prognosis ◽  
Stage Ia

Ovarian cancer is one of the main gynecological malignancies including cervical cancer and endometrial cancer. Epithelial ovarian cancer generally presents with already advanced disease at the time of diagnosis and is accompanied by poor prognosis. However, stage I ovarian cancer defined as lesions confined to the ovary is usually considered to have a good prognosis, illustrated by a 5-year survival rate of greater than 70–80%. Also, recurrences tend to be late and are usually in the abdominopelvic cavity. Metastases to the skeletal structures are rare. We report a rare case of early stage IA ovarian cancer, in which the first recurrent lesion was bone metastasis.

scholarly journals A rare case of endometrial cancer metastatic to the uveal choroid

2018 ◽  
Vol 23 ◽  
pp. 24-27 ◽  
Author(s):  
Stephanie H. Smith ◽  
Sri Krishna C. Arudra ◽  
Mary M. Mullen ◽  
Marguerite Palisoul ◽  
Sonika Dahiya ◽  
...  
Keyword(s):  
Endometrial Cancer ◽  
Rare Case

scholarly journals A Rare Case of Endometrial Cancer Metastatic to the Sigmoid Colon and Small Bowel

2017 ◽  
Vol 2017 ◽  
pp. 1-3
Author(s):  
Jeffrey A. Hubers ◽  
Anurag Soni
Keyword(s):  
Endometrial Cancer ◽  
Surgical Treatment ◽  
Small Bowel ◽  
Sigmoid Colon ◽  
Rare Case ◽  
Early Stage ◽  
Synchronous Metastases ◽  
Early Stage Endometrial Cancer

Metastatic endometrial cancer to the small bowel or colon has been described but is quite rare. We present a case of metastatic endometrial cancer with synchronous metastases to the colon and jejunum identified three years after surgical treatment of early stage endometrial cancer.

Sign in / Sign up

Export Citation Format

Share Document