Results 61 to 70 of about 4,417 (157)
ABSTRACT Groin swellings are the most frequent presenting clinical signs, which most frequently arise due to an inguinal hernia or lymphadenopathy. There are also rare congenital lesions, such as dermoid cysts, which can present similarly to common lesions, also leading to a diagnostic challenge.
Muhammad Hassaan Javaid +3 more
wiley +1 more source
Background Congenital inguinal hernia, hydrocele and undescended testis (UDT) are associated with patent processus vaginalis. The smooth muscles present in the processus vaginalis aid in the descent of the testis and undergo programmed cell death after ...
Nellai Krishnan +5 more
doaj +1 more source
Cell Block- A Useful Adjunct in Cytopathology of Serous Effusions [PDF]
Introduction: Use of the Cell Block (CB) technique in cytology increases the diagnostic accuracy. This technique enables cells to be retrieved in a fluid specimen to form a paraffin block, which concentrates the cells in a limited field without loss ...
Manoj Gopal Madakshira +3 more
doaj +1 more source
AMHR2 mutation in persistent Müllerian duct syndrome: A case of transverse testicular ectopia
Abstract Backgroud Persistent Müllerian duct syndrome (PMDS) is a rare condition characterized by the persistence of Müllerian duct structures in genotypic and phenotypic males. Case Presentation We present the case of a 4‐month‐old male with PMDS who presented with transverse testicular ectopia. The patient underwent diagnostic laparoscopic orchiopexy
Hangcheng Fu +2 more
wiley +1 more source
Hydrocele of canal of Nuck in an adult female: a case report
A hydrocele of canal of Nuck is a rare condition seen in females, commonly in the pediatric age group. The canal of Nuck is an extension of peritoneum into the inguinal canal through the deep ring, analogous to the processus vaginalis in males. Incomplete proximal obliteration and collection of serous fluid in the sac leads to the formation of a ...
Atish K. Parikh +4 more
openaire +2 more sources
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 +20 more
wiley +1 more source
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
Background: Urological pathologies of children are dominated by congenital malformations of the kidneys and urinary tract. Their management is often surgical.
Augustin Karl Agossou-Voyeme +4 more
doaj +1 more source
Insights Into Congenital Lymphatic Anomalies Underlying Fetal Effusions
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 +4 more
wiley +1 more source
Normozoospermic men in infertile couples: Potential benefit of early medical diagnostic procedures
Abstract Introduction Infertility, defined as the inability to achieve pregnancy despite regular, unprotected sexual intercourse for 1 year, affects approximately 15% of couples. Male factors contribute to 50% of these cases. The necessity of andrological evaluations for male partners of infertile couples with normozoospermia is currently under ...
Simone Bier +3 more
wiley +1 more source

