Results 11 to 20 of about 89,899 (262)

Abdominal-Pelvic Actinomycosis Mimicking Malignant Neoplasm [PDF]

open access: yesInfectious Diseases in Obstetrics and Gynecology, 2011
Abdominal-pelvic actinomycosis is often mistaken for other conditions, presenting a preoperative diagnostic challenge. In a 46-year-old female, computed tomography showed an abdominal-pelvic retroperitoneal mass extending from the lower pole of the right kidney to the lower pelvis. The patient had a 3-year history of intrauterine device.
Pusiol, Teresa   +3 more
openaire   +3 more sources

Gastrointestinal stromal tumour in Meckel's diverticulum

open access: yesWorld Journal of Surgical Oncology, 2007
Background Meckel's Diverticulum is the most commonly encountered congenital anomaly of the small intestine, occurring in approximately 2% of the population. Occasionally Meckel's diverticulum harbors neoplasms. Case presentation A 65 year old gentleman,
Patel Mahesh H   +6 more
doaj   +1 more source

Transvaginal Resection of an Ovarian Fibroma Presenting as Meigs Syndrome

open access: yesTaiwanese Journal of Obstetrics & Gynecology, 2005
Objective: Ovarian fibromas are benign neoplasms that arise from the stromal connective tissue of the ovary and constitute 4% of all ovarian neoplasms. We report a case of a twisted ovarian fibroma with ascites and mild pleural effusion which was removed
Wei-Hsi Chang   +2 more
doaj   +1 more source

Herlyn-Werner-Wunderlich syndrome with borderline serous cystadenoma of the ovary: case report and literature review

open access: yesRadiology Case Reports, 2021
Herlyn-Werner-Wunderlich syndrome, is a rare urogenital congenital anomaly. Coexisting Mullerian ducts anomalies and ovarian neoplasms are rarely reported.
Johara AlMulhim, MD   +1 more
doaj   +1 more source

Pelvic exenteration for locally advanced primary and recurrent pelvic neoplasm: a series of 54 resectable cases [PDF]

open access: yesEinstein (São Paulo), 2008
Objective: To report on a series of 54 patients with pelvic neoplasms submitted to curative pelvic exenteration at a tertiary hospital and describe the results (morbidity, mortality, and long-term survival).
Sergio Renato Pais Costa   +2 more
doaj  

Investigating the Protective Effects of Atorvastatin against Radiotherapy-Induced Gastrointestinal Toxicity in Abdominal and Pelvic Cancers: A Randomized, Double-Blind, Placebo-Controlled Trial [PDF]

open access: yesMiddle East Journal of Cancer
Background: Radiotherapy (RT) for pelvic cancers often causes gastrointestinal toxicity. While statins show promise in reducing radiation-induced injury through anti-inflammatory properties, their impact on acute toxicity remains unclear. The aim of this
Dr.Nadia Najafi Zade   +2 more
doaj   +1 more source

Prostatic sarcoma of the Ewing family in a 33-year-old male – A case report and review of the literature

open access: yesAsian Journal of Urology, 2016
Ewing sarcoma is the second most common primary bone tumor seen in children and adolescents, typically presenting between 10 and 20 years of age. Extraosseous sarcomas of the Ewing family in adults are rare. We report a manifestation of this tumor entity
Lukas Esch   +3 more
doaj   +1 more source

PROSTATE CANCER AND HIS INFLUENCE ON REPRODUCTIVE HEALTH

open access: yesActa Medica Leopoliensia, 2022
The aim of the study. Based on the data of the National Cancer Registry the research aims at conducting an analysis of morbidity and mortality of the male population of Ukraine for prostate cancer from 2014 to 2019. Materials and Methods.
Nataliya Medvedovska   +3 more
doaj   +1 more source

A Rare Abdomino-Pelvic Tumor: Paraganglioma

open access: yesActa Médica Portuguesa, 2015
Paragangliomas are rare tumors, with a reported incidence of 2–8 per million. They are chromaffin cell tumors that develop from the neural crest cells and may be divided in tumors derived from the parasympathetic or sympathetic ganglia. We report a case
Célia Pedroso   +4 more
doaj   +1 more source

Von Recklinghausen's disease with urogenital manifestation

open access: yesInternational Brazilian Journal of Urology, 2005
Neurofibromatosis or Von Recklinghausen's disease is a rare disease that affects the urogenital system in its visceral form. We report on one case where the patient had a recurring mass located in the vesicouterine space that caused irritative urinary ...
Thiago F. Nunes   +2 more
doaj   +1 more source

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