Results 61 to 70 of about 1,546 (185)

Capecitabine-induced cicatricial ectropion: A case review

The Pan-American Journal of Ophthalmology
Capecitabine, an oral prodrug of 5-fluorouracil (5-FU), offers a more targeted chemotherapeutic approach, reducing systemic side effects. However, cases of ocular side effects have been described in the literature. We report the case of a 94-year-old man
Stuti Misty Tanya, Andrea Dahoud, Ahmed Al-Amer, Bryan Arthurs, Christian El-Hadad   +4 more
doaj   +1 more source

An unusual complication after craniofacial surgery for Apert syndrome

Medical Journal of Dr. D.Y. Patil University, 2014
Apert syndrome is a rare genetic disorder, characterized by premature fusion of skull sutures, mid-face hypoplasia and syndactyly of the hands and feet. It is inherited as autosomal dominant or sporadic and is associated with increased paternal age.
Abhay A Lune, Bharat B Dogra, Sonali A Lune   +2 more
doaj   +1 more source

Eyelid fat grafting: indications, operative technique and complications; a systematic review

, 2016
International audienceIntroduction - Many recent studies concerning autologous fat grafting in the eyelids have been published, mostly consisting of case reports and retrospective case series. However, no study on the overall complication or satisfaction
Bannani, Sahar, Bertheuil, Nicolas, Boureaux, Elodie, Carloni, Raphael, Chaput, Benoit, De Runz, Antoine, Herlin, Christian, Mortemousque, Bruno, Mouriaux, Frédéric, Watier, Eric   +9 more
core   +3 more sources

S3 guideline: Diagnosis and treatment of epidermal necrolysis (Stevens‐Johnson syndrome and toxic epidermal necrolysis) – Part 2: Supportive therapy of EN in the acute and post‐acute stages

JDDG: Journal der Deutschen Dermatologischen Gesellschaft, Volume 22, Issue 11, Page 1576-1593, November 2024.
Summary Stevens‐Johnson syndrome and toxic epidermal necrolysis (SJS/TEN) are rare, predominantly drug‐induced, acute life‐threatening diseases of skin and mucosae. SJS and TEN are nowadays considered as variants of one disease entity with varying degrees of severity called epidermal necrolysis (EN).
Maren Paulmann, Ruben Heuer, Thorsten Annecke, Björn Behr, Katharina Boch, Anja M. Boos, Knut Brockow, Lars E. French, Jochen Gille, Verena Gundlach, Bernd Hartmann, Peter Höger, Silke C. Hofmann, Tobias Klein, Marcus Lehnhardt, Yvonne Liß, Philip Maier, Philipp Mandel, Nicos Marathovouniotis, Finnja Marlok, Hans Mittelviefhaus, Uwe Pleyer, Marie Pradeau, Katharina Rall, Siegbert Rieg, Heike Rittner, Frank Sander, Stefan Schnitzler, Christina Schut, Annette Stolle, Artem Vorobyev, Bettina Wedi, Johannes Weiss, Maximilian Zepp, Mirjana Ziemer, Maja Mockenhaupt, Alexander Nast   +36 more
wiley   +1 more source

Management of bilateral lower eyelid entropion in a black Angus bull by temporary tacking and modified Hotz Celsus

Veterinary Record Case Reports, Volume 12, Issue 3, September 2024.
Abstract The objective was to evaluate the progression and management of eyelid tacking sutures before permanent eyelid surgical correction. A 1‐year‐old Aberdeen black Angus bull presented with a 1‐month history of bilateral corneal ulcers. Ophthalmic examination revealed an infected stromal corneal ulcer on the left eye and bilateral lower eyelid ...
Leila Bedos, Anna Catherine Bowden, Jeff Olivarez, Melissa A. Kubai, Rachel A. Allbaugh   +4 more
wiley   +1 more source

Surgical Management of Severe Cicatricial Ectropion Secondary to Pityriasis Rubra Pilaris. [PDF]

Pityriasis rubra pilaris (PRP) is a rare inflammatory cutaneous disorder characterized by hyperkeratotic papules coalescing into red scaly plaques and palmoplantar keratoderma.Multiple noncutaneous findings for PRP have been reported, including subungual
Rubinstein, Daniel E, Sayed, Christopher J, Shams, Rayad B   +2 more
core   +2 more sources

Novel COL5A1 variants and associated disease phenotypes in dogs with classical Ehlers‐Danlos syndrome

Journal of Veterinary Internal Medicine, Volume 38, Issue 5, Page 2431-2443, September/October 2024.
Abstract Background Human patients with Ehlers‐Danlos syndrome (EDS) are categorized into subtypes based on causative genetic variants and phenotypes. The classical form of EDS, primarily caused by variants in COL5A1 or COL5A2, is a very common subtype in people but is poorly characterized in dogs.
Garrett Bullock, Jared A. Jaffey, Leah A. Cohn, Erika Sox, Eric T. Hostnik, Kyle D. Hutcheson, Erin Matero, Karen S. Hoffmann, Gary S. Johnson, Martin L. Katz   +9 more
wiley   +1 more source

Ocular Graft Versus Host Disease Following Allogeneic Stem Cell Transplantation: A Review of Current Knowledge and Recommendations [PDF]

, 2014
Graft versus host disease (GVHD) is a common complication of allogeneic stem cell transplantation (allo-SCT). Ocular GVHD develops in approximately 40-60% of patients following allo-SCT and its most common clinical manifestations include ...
Djalilian, Ali R., Eslani, Medi, Mehravaran, Shiva, Nassiri, Nariman, Panahi, Nekoo, Ziaei, Alireza   +5 more
core   +1 more source

A Clinical Masquerader: Squamous Cell Carcinoma of the Eyelid Previously Diagnosed as an Eye Bump [PDF]

, 2019
Malignant eyelid tumors are often difficult to diagnose at early stage growth, and can be clinically challenging. Due to the high prevalence of periocular skin cancers, clinicians must be very attentive in their assessment of skin lesions amongst their ...
Fisher, April J., Fisher, Brian D., Rodriguez, Alexis, Virk, Sanjeet Kaur   +3 more
core   +2 more sources

How does ocular graft‐versus‐host disease fit under the dry eye umbrella? A review

Clinical &Experimental Ophthalmology, Volume 52, Issue 2, Page 167-185, March 2024.
Abstract Graft‐versus‐host disease (GVHD) is a systemic disease that can affect multiple organs as a consequence of an allogeneic haematopoietic stem cell transplant. One organ system that is often affected in GVHD is the eyes. Ocular GVHD (oGVHD) may involve various structures within the eye including the lacrimal glands, eyelids, conjunctiva, cornea,
Nicole B. Kantor, Arianna Tovar, Trent Wang, Anat Galor   +3 more
wiley   +1 more source