Results 221 to 230 of about 63,442 (308)

A Case of Malignant Brenner Tumor With High FDG Uptake

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Malignant Brenner Tumor (MBT) is a rare malignant neoplasm originating from the ovarian surface epithelium. This type of tumor typically lacks specific clinical manifestations and dedicated tumor markers. In our case, we present a complete set of clinical information, diagnosis and treatment protocols, and follow‐up results of one case of MBT.
Jie Li   +3 more
wiley   +1 more source

Embryonal Paratesticular Rhabdomyosarcoma Masquerading as an Inguinal Hernia: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Embryonal paratesticular rhabdomyosarcoma can mimic benign inguinoscrotal conditions such as inguinal hernia. In children with persistent, painless scrotal masses, early cross‐sectional imaging and prompt radical inguinal orchiectomy with histopathological confirmation are essential.
Somaya Al Kiswani   +7 more
wiley   +1 more source

Stage IIIC Bilateral Dysgerminoma in a 16‐Year‐Old Phenotypic Female With 46,XY Complete Gonadal Dysgenesis and Primary Amenorrhea: A Case Report

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Dysgerminoma, the most common malignant ovarian germ cell tumor, has a significantly increased incidence in individuals with 46,XY complete gonadal dysgenesis (Swyer syndrome). However, primary amenorrhea is the hallmark presentation of Swyer syndrome in adolescence.
Mahshid Vasef   +4 more
wiley   +1 more source

Potential of Retrospective Fusion of FDG PET and Abbreviated MRI in Posttreatment Oral Cancer Follow-Up Using NI-RADS: Largest Case Series from a Tertiary Cancer Center in Western India

open access: yesIndian Journal of Radiology and Imaging
Diva Shah   +6 more
doaj   +1 more source

Bilateral Gonadoblastoma in a 12‐Year‐Old Girl 4 Years After Wilms' Tumor: A Rare Pediatric Case

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT This case of a 12‐year‐old patient who developed bilateral gonadoblastoma 4 years after treatment for Wilms tumor highlights the importance of rigorous, risk‐adapted long‐term surveillance and careful evaluation of incidental gonadal findings, even in asymptomatic patients.
Ahmed Quraish   +4 more
wiley   +1 more source

Effect of dual trigger on pregnancy outcomes in women with diminished ovarian reserve: A single-blind randomized clinical trial. [PDF]

open access: yesInt J Reprod Biomed
Zamaniyan M   +6 more
europepmc   +1 more source

A Rare Coexistence: Uterine Leiomyoma Arising in a Mature Cystic Teratoma and a Pedunculated Endometriotic Cyst Mimicking Leiomyoma—Two Case Reports

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Uterine leiomyomas are common benign tumors, but their clinical presentation can be misleading. We report two unusual cases of pedunculated uterine masses presenting with heavy vaginal bleeding. In the first case, a woman in her 40s underwent urgent resection of a prolapsing mass after acute hemorrhage; histopathological examination ...
Mena Abdalla   +9 more
wiley   +1 more source

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