Results 71 to 80 of about 25,515 (288)

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

Andrology, EarlyView.
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

A child presenting with bullous emphysema

The Turkish Journal of Pediatrics, 2022
Background. Placental transmogrification of the lung (PTL) is a clinical spectrum varying from asymptomatic to severe pulmonary impairment; such as recurrent pneumothorax, bronchopneumonia, respiratory distress syndrome and chronic obstructive ...
Beste Özsezen, Uğur Özçelik, Deniz Doğru, Ebru Yalçın, Diclehan Orhan, Tutku Soyer, Nagehan Emiralioğlu, Elnur Nurullayev, H Nursun Özcan, Meral Üner, Dilber Ademhan Tural, Nural Kiper   +11 more
doaj   +1 more source

Cowden syndrome - Diagnostic skin signs [PDF]

, 2001
Cowden syndrome is a rare autosomal dominant familial cancer syndrome with a high risk of breast cancer. The most important clinical features include carcinomas of the breast and thyroid, and hamartomatous polyps of the gastrointestinal tract.
Burgdorf, Walter H. C., Hildenbrand, C., Lautenschlager, Stephan   +2 more
core   +1 more source

Detection of the Heterozygous Recurrent MAX p.(Arg60Gln) Variant in Two Females Confirms and Expands the Phenotypic Spectrum of Polydactyly–Macrocephaly Syndrome

Clinical Genetics, EarlyView.
We identified a recurrent heterozygous MAX c.179G>A:p.Arg60Gln variant in two unrelated females affected with the emerging phenotypes of MAX‐associated polydactyly‐macrocephaly syndrome. We propose that genitourinary abnormalities, including Mayer–Rokitanski–Kuster–Hauser syndrome in one individual, are an expansion of the known phenotypes associated ...
Iftekhar A. Showpnil, Neta Feinstein‐Goren, Lior Greenbaum, Ortal Barel, Daniel C. Koboldt, Samantha A. Brugmann, Kathryn Nicole Weaver, Anne Slavotinek, Ben Pode‐Shakked, Rolf W. Stottmann   +9 more
wiley   +1 more source

Urban Lymphatic Filariasis in the Metropolis of\ud Dar es Salaam, Tanzania [PDF]

, 2013
The last decades have seen a considerable increase in urbanization in Sub-Saharan Africa, and it is estimated that over 50% of the population will live in urban areas by 2040.
Malecela, Mwelecele N, Mosha, Franklin W, Mwakitalu, Mbutolwe E, Pedersen, Erling M, Simonsen, Paul E   +4 more
core  

Laparoscopic Excision of Hydrocele of the Canal of Nuck in an Adult Female Using the "Open Posterior Wall Technique": Case Report Describing a Novel Laparoscopic Approach.

Journal of Nippon Medical School = Nippon Ika Daigaku zasshi, 2019
Complete surgical excision is the standard treatment for hydrocele of the canal of Nuck. Accordingly, we devised a novel open posterior wall technique for laparoscopic transabdominal preperitoneal (TAPP) excision.A 38-year-old woman presented to us with ...
N. Chihara, N. Taniai, Hideyuki Suzuki, R. Nakata, Mio Shioda, H. Yoshida   +5 more
semanticscholar   +1 more source

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, EarlyView.
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

Overexpression of Aquaporin 1 in the Tunica Vaginalis May Contribute to Adult-Onset Primary Hydrocele Testis

Advances in Urology, 2014
To investigate the cause of the adult-onset primary noncommunicating hydrocele testis, protein expressions of water channel aquaporins (AQPs) 1 and 3 in the tunica vaginalis were assessed.
Mami Hattori, Akiko Tonooka, Masayoshi Zaitsu, Koji Mikami, Ayako Suzue-Yanagisawa, Toshimasa Uekusa, Takumi Takeuchi   +6 more
doaj   +1 more source

Scrotal Ultrasound Is Not Routinely Indicated in the Management of Cryptorchidism, Retractile Testes, and Hydrocele in Children

Global Pediatric Health, 2019
Cryptorchidism, or undescended testes, is the most common congenital genitourinary anomaly. A failure or delay of treatment may result in reduced fertility or an increased risk of testicular cancer.
L. Shields, Jeffrey T White, D. Peppas, Eran Rosenberg   +3 more
semanticscholar   +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