Results 111 to 120 of about 8,516 (258)
Case Reports in Ophthalmological Medicine, Volume 2025, Issue 1, 2025.Goldenhar syndrome (GS), also known as Franceschetti–GS, encompasses a spectrum of congenital anomalies affecting the eyes, ears, face, and vertebrae. This case report highlights a 2‐day‐old female patient diagnosed with GS presenting a rare manifestation of bilateral complete eyelid colobomas.
Rawan S. Utt +6 more
wiley +1 more source
Pleomorphic adenoma with extensive squamous metaplasia and keratin cyst formations in minor salivary gland: a case report [PDF]
, 2011 Pleomorphic adenoma (PA), the most common salivary gland tumor, accounts for 54 to 65% of all salivary gland neoplasias and 80% of the benign salivary gland tumors. It most frequently affects the parotid gland, followed by the submandibular and the minor
Carlos-Bregni, Roman +6 more
core +5 more sources
Encephalocraniocutaneous Lipomatosis Associated with Orbital Cyst: A Variant or New Entity?
Türk Oftalmoloji Dergisi, 2021 Encephalocraniocutaneous lipomatosis (ECCL), also known as Haberland or Fishman syndrome, is an extremely rare congenital neurocutaneous disorder that characteristically involves ectomesodermal tissues such as the central nervous system, eyes, and skin ...
Abubakar Garba Farouk +4 more
doaj +1 more source
Heterotopic gastrointestinal cyst mimicking chronic cholecystitis: a case report [PDF]
, 2008 Introduction Heterotopic gastric mucosa is described almost everywhere in the gastrointestinal tract, from the oral cavity to the rectum. The occurrence of heterotopic gastric tissue in the gallbladder is rare. A choristoma can be defined as a new growth
AJ Yoon +16 more
core +3 more sources
Cysts and tumours of the iris: Diagnostic tools and key management considerations—A review
Clinical &Experimental Ophthalmology, Volume 52, Issue 6, Page 665-683, August 2024.Abstract The iris is a unique structure, with exquisite variations in colour and form. Pathological changes, specifically including iris cysts and tumours are relatively uncommon, difficult to diagnose, and yet potentially blinding or life‐threatening.
Bia Z. Kim +2 more
wiley +1 more source
Accessory cavitated uterine malformation (ACUM): A scoping review
Acta Obstetricia et Gynecologica Scandinavica, Volume 103, Issue 6, Page 1036-1045, June 2024.Accessory cavitated uterine malformation is a distinct, yet unclassified uterine anomaly. This systematic review summarizes diagnostic and clinical findings as well as management strategies from all described cases in the literature and suggests unified diagnostic criteria and definitions. Abstract Introduction Accessory cavitated uterine malformation (
Stefan Timmerman +5 more
wiley +1 more source
Bovine congenital defects recorded by veterinary practitioners
Reproduction in Domestic Animals, Volume 59, Issue 1, January 2024.Abstract A mobile phone app was used by 59 veterinary practitioners to collect case histories and images of 191 cattle with congenital defects distributed nationally over a 3‐year period. The majority of cases were recorded during the spring calving season (57.6%) in pluriparous dairy dams.
J. F. Mee, D. Murphy, M. Curran
wiley +1 more source
Optic Nerve: Developmental Anomalies and Common Tumors [PDF]
, 2018 The optic nerve, also known as the second cranial nerve, is composed of axons that transmit visual information from the neurosensory retina to the visual cortex. There are multiple pathologies that can affect the human optic nerve.
Alkatan, Hind +2 more
core +2 more sources
Case Reports in Ophthalmological Medicine, Volume 2024, Issue 1, 2024.Objective: To describe the morphological and histopathological features of primary conjunctival basal cell carcinoma (BCC) in a young adult Filipino. Introduction: Malignant conjunctival tumors arise from different cells, the most common of which are squamous cell carcinomas (SCCs), (including ocular surface squamous neoplasia [OSSN]), melanomas, and ...
Lorenz Jacob Mangahas +3 more
wiley +1 more source
Ectopic Liver Tissue on Gallbladder (Choristoma): Two Case Reports.
, 2021 erdem sarı
openalex +1 more source