Results 11 to 20 of about 5,407 (151)
Embryonal Paratesticular Rhabdomyosarcoma Masquerading as an Inguinal Hernia: A Case Report. [PDF]
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.
Al Kiswani S +7 more
europepmc +2 more sources
Paraspinal Extrarenal Wilms Tumor Case Report and Review of Literature. [PDF]
Introduction Extrarenal Wilms tumors (ERWTs) (i.e., nephroblastoma) are exceptionally rare tumors that have only been reported approximately 100 times in the literature. These tumors necessitate histology (rather than imaging) for proper identification, often resulting in a postoperative diagnosis.
Barbaro JL +3 more
europepmc +2 more sources
Embryonal rhabdomyosarcoma of the adult prostate: case report and review
Herein is reported a case of embryonal rhabdomyosarcoma of the prostate in a 54-year-old male. The presenting symptoms were dysuria, hematuria, and systemic thrombotic events. Diagnosis was ascertained through a transurethral resection.
Jeffrey Johnson +5 more
doaj +1 more source
Aims This study aimed to identify the optimal human chorionic gonadotropin (hCG) ratio in predicting etoposide, methotrexate, dactinomycin, cyclophosphamide, and vincristine resistance in women diagnosed with high‐risk gestational trophoblastic neoplasia
Nathapol Sirimusika, Sathana Boonyapipat
doaj +1 more source
Treatment of low-risk gestational trophoblastic neoplasia comparing biweekly eight-day Methotrexate with folinic acid versus bolus-dose Actinomycin-D, among Brazilian women [PDF]
PURPOSE: To compare two single-agent chemotherapy (ChT) regimens evaluating, in first-line treatment, response and side effects and, in final single-agent treatment, the outcomes, among Brazilian patients with low-risk gestational trophoblastic neoplasia
Elza Maria Hartmann Uberti +5 more
doaj +2 more sources
Choriocarcinoma is a malignant trophoblastic tumour usually of placental origin. It is characterized by early metastasis to the brain and lungs. With early detection, it has a better prognosis with treatment.
Sunil Kumar Das +2 more
doaj +1 more source
Prolonged Survival With Homozygous Deletion of Exon 9 in Perlman Syndrome: A Case Report. [PDF]
Perlman syndrome is a rare autosomal recessive overgrowth disorder characterized by macrosomia, nephromegaly, renal dysplasia, and characteristic facial features. It has both similarities and differences to other more common overgrowth syndromes. Pathogenic homozygosity is extremely rare in nonconsanguineous relationships.
Levy E, Elliott L, Miller MA, Kramer M.
europepmc +2 more sources
Drug Repurposing Against SARS-CoV-2: Targeting NSP16-NSP10 Interaction
Drug repurposing studies played an important role for fighting with the Covid-19 pandemic. Discovering a new drug molecule for a disease takes a very long time. However, repurposing a drug molecule developed for another disease can accelerate to find new
Sefer BADAY
doaj +1 more source
Choriocarcinoma brain metastasis in a patient in the third trimester: a case report
Background Metastatic choriocarcinoma in the third trimester of pregnancy is extremely rare. Case presentation A 25-year-old Chinese woman (gravida 3, para 0) who was 28 weeks pregnant was admitted for sudden convulsion, aconuresis, and unconsciousness ...
Chunjuan Shen +5 more
doaj +1 more source
An unusual presentation of neonatal rhabdomyosarcoma: a case report
A full-term infant with an unremarkable prenatal course presented at birth with a large midline facial mass and smaller masses in the head and neck. In addition, multiple diffuse flesh-colored nodules spread along all the upper and lower limbs.
Danielle Strah +7 more
doaj +1 more source

