Results 61 to 70 of about 28,589 (204)
Clinical Profile of Unilateral Proptosis in a Tertiary Care Centre
Proptosis, the forward protrusion of the eyeball, is a common manifestation of a wide variety of diseases inside the orbit and its spaces. Its diagnosis is usually a combined effort of the ophthalmologist, otolaryngologist, neurosurgeon, and radiologist.
S. Dsouza +3 more
semanticscholar +1 more source
This report describes a nano magnesium nourisher, named MgC@PS, capable of targeted Mg2⁺ delivery to macrophages, effectively suppressing The nuclear factor kappa B (NF‐κB) activation and mitigating NLRP3 inflammasome‐driven pyroptosis in liver inflammation.
Li Wang +13 more
wiley +1 more source
Unusual Presentation of Orbital Neuroblastoma after Evisceration
This is a case report of a 17 year old girl having protruding mass from evicerated left eye which was associated with severe ocular pain. Mass was about 3.6 × 5.8 cm in size, histopathological examination and immunohistochemistry report confirm ...
Swati Kujur, Devesh Khandey
doaj +1 more source
A Giant Fronto-Ethmoidal Osteoma Presenting With Proptosis and Diplopia [PDF]
Derya Güçlü +3 more
openalex +1 more source
Extranodal Lymphoplasmacytic Lymphoma Responding Rapidly to Zanubrutinib: A Case Series
ABSTRACT Management of recurrent or atypical lymphoplasmacytic lymphoma poses a significant therapeutic challenge. Here we demonstrate a case series of three patients with atypical presentations of extranodal lymphoplasmacytic lymphoma that each show remarkable and timely responses to Zanubrutinib with a limited side effect profile.
Samuel Brown +3 more
wiley +1 more source
Orbital Metastasis of Cervical Carcinoma – Case Report and Review of Literature [PDF]
The orbit is a frequent site of metastasis, particularly from the breast, prostate gland and the lung. Carcinoma of the cervix metastasizing to the orbit is rare.
Anupriya Arthur +5 more
doaj +1 more source
A Rare NPHS2 Mutation (E130K) in Hereditary Steroid‐Resistant Nephrotic Syndrome: A Case Report
Hereditary steroid‐resistant nephrotic syndrome (HSRNS) due to mutations in the NPHS2 gene (encoding podocin) is a rare genetic condition that typically presents in childhood. We report a case of a 2‐year‐and‐8‐month‐old male, the seventh child of consanguineous parents, who presented with recurrent fever, febrile tonic‐clonic seizures, and periorbital
Ramzi Hmedan Mujahed +7 more
wiley +1 more source
Nontraumatic subperiosteal orbital hemorrhage following upper gastrointestinal endoscopy
Subperiosteal hemorrhages are typically the result of blunt orbital or facial trauma. Nontraumatic subperiosteal hemorrhages are uncommon and are usually attributed to increase in central venous pressure and bleeding disorders.
Swaranjali S Gore +7 more
doaj +1 more source
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
Chronic lymphocytic leukemia presenting as unilateral extraocular muscle enlargement and proptosis
Orbital involvement in chronic lymphocytic leukemia (CLL) is rare with very few published cases. We describe a case of unilateral isolated extraocular muscle enlargement in a patient with CLL.
Amun Sachdev +2 more
doaj +1 more source

