Results 61 to 70 of about 20,087 (270)

Laparoscopic Partial Splenectomy for a Giant Congenital Splenic Cyst in a Child: Case Report and Focused Literature Review

open access: yesClinical Case Reports, Volume 14, Issue 1, January 2026.
ABSTRACT An 11‐year‐old boy with a 16 × 14.5 cm congenital splenic cyst underwent laparoscopic upper‐pole partial splenectomy after negative hydatid workup and vaccination. Recovery was uneventful; histology confirmed epithelial cyst. Spleen‐preserving surgery provided durable symptom relief and preserved function.
Ahmed Alanzi   +5 more
wiley   +1 more source

Epidermoid Cyst of Spleen [PDF]

open access: yes, 2010
Splenic cysts are very rare lesions, most of them being parasitic systs. Nonparasitic cysts are uncommon. We report a case of young female who presented with mass and pain abdomen. Ultrasound examination revealed splenic syst. The diagnosis of epidermoid
Usha, R, Vijay Shankar, S
core   +1 more source

Imaging in gynecological disease (29): clinical and ultrasound features of primary ovarian immature teratoma

open access: yesUltrasound in Obstetrics &Gynecology, Volume 67, Issue 1, Page 89-99, January 2026.
ABSTRACT Objective To describe the clinical and ultrasound characteristics at the time of diagnosis of primary ovarian immature teratoma with no other germ cell tumor components described on histopathology. Methods This was a retrospective study of women with a histological diagnosis of primary ovarian immature teratoma who had undergone a preoperative
C. Landolfo   +33 more
wiley   +1 more source

Surgical treatment of intradiploic epidermoid cyst treated as depression [PDF]

open access: yes, 2014
Introduction. Extradural intradiploic epidermoid cysts are rare, representing less than 0.25% of all primary intracranial tumors. They can be neurologically silent and can only present psychiatric symptoms like depression, cognitive or ...
Jovanović Milan   +3 more
core   +1 more source

Multiple Nodules in a Newborn

open access: yes
JEADV Clinical Practice, EarlyView.
Flora Balieva   +5 more
wiley   +1 more source

Molecular pathology of testicular germ cell tumours: an update for practicing pathologists

open access: yesHistopathology, Volume 88, Issue 1, Page 214-229, January 2026.
Molecular testing for isochromosome 12p is usually only necessary in difficult cases that encompass metastases or recurrent diseases including somatic‐type malignancies. So far, no breaking progress has been made in the field of targeted therapy as TGCTs only rarely show targetable molecular alterations.
Alexander Fichtner   +3 more
wiley   +1 more source

Dermoid cyst of the pancreas: presentation and management

open access: yesWorld Journal of Surgical Oncology, 2007
Background Dermoid cyst of the pancreas is a benign, well-differentiated, extremely rare germ cell neoplasm. Published data indicate that differential diagnosis of cystic lesions of the pancreas is challenging and although ultrasonography, computed ...
Amabile Dalia   +6 more
doaj   +1 more source

Intramedullary Dermoid Cyst- A Rare Case Report [PDF]

open access: yes, 2014
A 35 years old male came with complaints of low back ache radiating to right lower limb and is associated with tingling numbness and thin stream of urine since 1 year.
Abhijit Patil   +3 more
core  

Recurrence of congenital dermoid cyst of paramedian location [PDF]

open access: yes, 2010
INTRODUÇÃO: O cisto dermoide é um cisto de desenvolvimento incomum na face e envolve mais frequentemente o assoalho bucal. A maioria das lesões ocorre em adultos jovens, com ligeira predileção pelo gênero masculino.
MACHADO, Gustavo Grothe   +4 more
core   +3 more sources

A Rare Case of Nasal Chondromesenchymal Hamartoma Presenting With Respiratory Distress in a Newborn: A Case Report

open access: yesCase Reports in Otolaryngology, Volume 2026, Issue 1, 2026.
Introduction Nasal chondromesenchymal hamartoma (NCMH) is a rare cause of nasal mass in infants and children. It was first described in 1998, and since then, only 63 previous cases have been reported. Case Report Here, we report a case of a 4‐day‐old neonate with a right‐sided nasal mass presenting with respiratory distress since birth.
Mikiyas Olani   +6 more
wiley   +1 more source

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