Results 61 to 70 of about 16,751 (207)

Adult granulosa cell tumours of the testis analogous to ovarian counterparts are exceptionally rare: analysis of a multicentric series and review of the literature

Histopathology, Volume 88, Issue 4, Page 831-842, March 2026.
Assessment of twenty testicular AGCTs with two different next‐generation sequencing (NGS) panels reveals differences with ovarian AGCTs, including absence of hotspot FOXL2 variants. Aims Testicular adult granulosa cell tumours (AGCTs) are rare and show several clinical–pathological differences with their ovarian counterparts.
Costantino Ricci, Dario de Biase, Thais Maloberti, Agnese Orsatti, Thomas M Ulbright, Muhammad T Idrees, Esther Oliva, Kristine Cornejo, João Lobo, Kvetoslava Michalova, Maria Rosaria Raspollini, Sean R Williamson, Geert JLH van Leenders, Chia‐Sui Kao, Fiona Maclean, Ankur R Sangoi, Adeboye O Osunkoya, Michelangelo Fiorentino, Antonio De Leo, Giovanni Tallini, Andres Martin Acosta   +20 more
wiley   +1 more source

Global prevalence of hydrocele in infants and children: a systematic review and meta-analysis

BMC Pediatrics
Background Pediatric hydrocele is a congenital pathology commonly diagnosed in newborns. Also, untreated pediatric hydrocele can induce adverse permanent consequences in adulthood.
Nader Salari, Mahan Beiromvand, Reza Abdollahi, Fuzieh Khani Hemmatabadi, Alireza Daneshkhah, Amirhoussain Ghaderi, Maryam Asgari, Masoud Mohammadi   +7 more
doaj   +1 more source

Comparison of two method of hydrocele repair in children

Iranian Journal of Pediatric Surgery, 2019
Introduction: Hydroceles is accumulation of fluid in the processus vaginalis (PV) resulting in swelling of the inguinal region or scrotum. Its treatment depends on age, symptoms and conection with abdomen.
Omid Amanollahi, Zahra Ghasem nejad, Ardalan Samadzadegan   +2 more
doaj   +1 more source

Diagnosis and management of testicular compartment syndrome caused by tension hydrocele

Urology Case Reports, 2022
A hydrocele is an abnormal collection of fluid within the tunica vaginalis which may either be congenital or acquired. Hydroceles are usually painless and don't require immediate intervention unless they impact activities of daily living.
Irene Chen, Sohrab Arora, Kenan Alhayek, David Leavitt, Ali Dabaja   +4 more
doaj   +1 more source

Clinical and Genetic Significance of Chromosomal Microarray Screening of Asymptomatic Newborns

Journal of Clinical Laboratory Analysis, Volume 40, Issue 3, February 2026.
Among 99 asymptomatic newborns with abnormal low‐resolution chromosomal microarray (LR‐CMA) screening, 70.7% harbored microduplication/microdeletions with syndromic implications. However, only a minority exhibited developmental concerns during early follow‐up, highlighting the need for cautious interpretation.
Naye Choi, Hwa Young Kim, Jung Min Ko
wiley   +1 more source

Hydrocele

The Professional Medical Journal, 2008
Introduction: A hydrocele is an abnormal collection of serous fluid withinthe tunica or processes vaginalis. It is treated by surgery and sclerotherapy. Objectives: To compare the results ofsurgery and sclerotherapy in the treatment of scrotal hydrocele. Design: Randomized control trial.
Vaithianathan Natarajan, Neil Oakley
  +5 more sources

Detection of germ cell neoplasia in situ and testicular cancer risk in men with testicular microlithiasis: Real world results through 10 years

Andrology, Volume 14, Issue 2, Page 459-465, February 2026.
Abstract Background Guidelines recommend biopsies for men <50 years with testicular microlithiasis and cancer risk factors to rule out germ cell neoplasia in situ. Limited data support this practice. Objectives To clarify the significance of testicular microlithiasis by examining pathological findings in men with testicular microlithiasis.
Karoline Skov Lundager, Rasmus Hassing Frandsen, Emil Durukan, Nadia Zeeberg Belhouche, Christian Fuglesang S. Jensen, Peter Busch Østergren, Jens Sønksen, Mikkel Fode   +7 more
wiley   +1 more source

KBG Syndrome: A Case Report and Longitudinal Assessment of Long‐Acting Recombinant Human Growth Hormone Therapy

Clinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT This case analysis examines the clinical data, molecular genetic testing results, and 20‐month clinical data of long‐acting recombinant human growth hormone (rhGH) treatment in a child with KBG syndrome (KBGS). The child exhibited a c.1591delG frameshift mutation in the ANKRD11 gene associated with KBGS, a variant not previously reported ...
Hui Nan, Pu Zhang, Jing Qian
wiley   +1 more source

Lymphatic filariasis in Luangwa District, South-East Zambia [PDF]

, 2013
BACKGROUND: Past case reports and recent data from LF mapping surveys indicate that LF occurs in Zambia, but no studies have been carried out to document its epidemiology and health implications.
Enala T Mwase, Erling M Pedersen, Paul E Simonsen, Sheila Shawa   +3 more
core   +1 more source

Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions

Prenatal Diagnosis, Volume 46, Issue 1, Page 3-11, January 2026.
ABSTRACT Objective We describe a series of pregnancies with autosomal dominant lymphedema and generalized lymphatic dysplasia in the fetus diagnosed with prenatal exome or genome sequencing. We focus on specific syndromes, fetal features, and parental symptoms to deepen our understanding of congenital lymphatic anomalies.
Sara G. Vargo, Daniella Rogerson, Patrick Devine, Jessica Van Ziffle, Teresa N. Sparks   +4 more
wiley   +1 more source