Zobrazeno 1 - 10
of 626
pro vyhledávání: '"scrotal mass"'
Autor:
Jaafar Fouimtizi, Youssef Maachi, Anass Rhayour, Amine EL Boustani, Amine Slaoui, Tariq Karmouni, Khalid EL Khader, Abdellatif Koutani, Ahmed Iben Attya Andaloussi
Publikováno v:
Urology Case Reports, Vol 54, Iss , Pp 102747- (2024)
Liposarcomas are an uncommon occurrence in the paratesticular region that makes about 20 % of all sarcomas. The clinical appearance is an inguinal lump, which can resemble a hydrocele or hernia. There would be no conventional treatment accessible bec
Externí odkaz:
https://doaj.org/article/f27ce4794e9e403185e3cc2c463c5382
Autor:
Ramona Montironi, Stefano Raffaele Giannubilo, Irene Cappanera, Giovanna Irene Battistoni, Romina Mancinelli, Andrea Ciavattini
Publikováno v:
Healthcare, Vol 12, Iss 5, p 583 (2024)
Inguinoscrotal hernia is a common pediatric disease but a rare condition in the fetus. We present a case, from our institution, of fetal inguinoscrotal hernia with possible rapid development. In addition to our case, we present a literature update on
Externí odkaz:
https://doaj.org/article/04baad1da23441e9a49200bcc5cc739b
Publikováno v:
Urology Case Reports, Vol 50, Iss , Pp 102507- (2023)
Scrotal lymphangioma is a rare, acquired, idiopathic conditions. Surgical resection can result in successful outcomes. A 43-year-old man presented with a painless scrotal mass. Ultrasonography and magnetic resonance imaging revealed a multifocal cyst
Externí odkaz:
https://doaj.org/article/f97be8f8163b463ab084997b8f687056
Publikováno v:
Frontiers in Oncology, Vol 13 (2023)
Paratesticular liposarcoma (PLS) causes scrotal mass changes, rarely in the urinary system. Before surgery, PLS causes scrotal mass changes that are difficult to distinguish from other causes. There has been a report of a giant paratestis liposarcoma
Externí odkaz:
https://doaj.org/article/e816bb201dbd40f79721cd8e25498be1
Autor:
Orgeness Jasper Mbwambo, Angela Pallangyo, Jasper Saidi Mbwambo, Frank Bright, Alfred K. Mteta, Jacques Bogdanowicz, Bartholomeo Nicholaus Ngowi
Publikováno v:
Clinical Case Reports, Vol 11, Iss 6, Pp n/a-n/a (2023)
Abstract Primary scrotal lipoma is a rare urological diagnosis. It is usually diagnosed incidentally as most of time initial diagnosis may be confused with other common etiology of scrotal masses. A rare case of scrotal lipoma with initial misdiagnos
Externí odkaz:
https://doaj.org/article/18b890dae81e4bfebca09b58c6eee755
Akademický článek
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Publikováno v:
Journal of Psychiatry Spectrum, Vol 1, Iss 2, Pp 136-139 (2022)
Anti-N-methyl-D-aspartate receptor (NMDAr) encephalitis is an autoimmune encephalitis that commonly presents with various neurobehavioral symptoms. Anti-NMDAr encephalitis is known to occur more commonly in young females with teratoma. In this case,
Externí odkaz:
https://doaj.org/article/657f8b2bc8654789a85233f508a50a49
Autor:
Léonidas Nyandwi, Salahoudine Idrissa, Hellé Moustapha, Mahamoud Omid Ali Ada, Efared Boubacar, Idrissa Boubacar, Zakhama Abdelfatteh, Ksia Amine, Abarchi Habibou
Publikováno v:
Journal of Medical Case Reports, Vol 16, Iss 1, Pp 1-5 (2022)
Abstract Background Aggressive angiomyxoma (AAM) is a locally infiltrative mesenchymal tumour that most commonly affects the pelvis and/or perineum in adult women. AAM is very rare in males, especially in infancy. Case presentation A 10-month-old ful
Externí odkaz:
https://doaj.org/article/5dc061e1e0244da286b77b6f2d12d344
Autor:
Leen Alkukhun, MD, Alyssa Ionno, MD, Meghan Stanton, MD, Serenella Serinelli, MD, PhD, Ryan Baker, BS, Ravikumar Hanumaiah, MD, Anand Majmudar, MD
Publikováno v:
Radiology Case Reports, Vol 17, Iss 6, Pp 2191-2194 (2022)
Splenogonadal fusion is a rare, frequently misdiagnosed, congenital anomaly in which the splenic tissue is abnormally attached to the gonadal or mesonephric remnants. It is commonly found as an incidental finding at autopsy, during orchiopexy or hern
Externí odkaz:
https://doaj.org/article/14f3fa3e8e074eb9b17babf3f6f8297c
Autor:
Magdalena Ostrowska, Piotr Świniarski, Adam Ostrowski, Filip Ryszard Kowalski, Jan Adamowicz, Dariusz Grzanka, Tomasz Adam Drewa, Kajetan Juszczak
Publikováno v:
Basic and Clinical Andrology, Vol 32, Iss 1, Pp 1-6 (2022)
Résumé Contexte La sarcoïdose est une maladie multisystémique caractérisée par la formation de granulomes non caséeux dans divers organes. Les poumons restent l’organe le plus fréquemment touché, alors que les lésions du système génito-
Externí odkaz:
https://doaj.org/article/6ae6624418184ece9fe2ccccbb81e158