Please use this identifier to cite or link to this item: http://hdl.handle.net/11452/21782
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dc.contributor.authorMatsumoto, Yukihiro-
dc.contributor.authorTsubota, Kazuo-
dc.date.accessioned2021-09-08T10:51:42Z-
dc.date.available2021-09-08T10:51:42Z-
dc.date.issued2005-
dc.identifier.citationMatsumoto, Y. vd. (2005). "Ocular surface findings in Hallopeau-Siemens subtype of dystrophic epidermolysis bullosa - Report of a case and literature review". Cornea, 24(4), 474-479.en_US
dc.identifier.issn0277-3740-
dc.identifier.urihttps://doi.org/10.1097/01.ico.0000151722.84634.bf-
dc.identifier.urihttps://journals.lww.com/corneajrnl/Fulltext/2005/05000/Ocular_Surface_Findings_in_Hallopeau_Siemens.19.aspx-
dc.identifier.urihttp://hdl.handle.net/11452/21782-
dc.description.abstractPurpose: This article describes the clinical features and long-term changes in corneal sensitivity, tear function, and impression cytology findings in a patient with recessive dystrophic epidermolysis bullosa (DEB). Methods: The patient underwent best-corrected Landolt visual acuity measurements, slit-lamp examinations, anterior segment photography, Schirmer test with anesthesia, tear film break-up time, corneal fluorescein and Rose-Bengal staining, assessment of corneal sensitivity, and conjunctival impression cytology at the initial and final visits. Results: The patient had a recurrent corneal erosion in the right eye and a painful corneal blister with extensive superficial punctuate keratopathy in the left eye, which remained refractory to treatment with patching, lubricants, and antibiotic ointments for 10 weeks. The corneal disease in both eyes responded swiftly to topical fibronectin, topical nonpreserved tears, vitamin A ointment, and therapeutic soft contact lenses. Maintenance treatment was continued with preservative-free topical tear drops and vitamin A ointment. Corneal disease did not recur in the patient during the follow-up of 29 months. The mean corneal sensitivity and tear film break-up time were decreased initially in both eyes and attained normal values with treatment. Impression cytology revealed squamous metaplasia, loss of cellular cohesion, and total absence of goblet cells before treatment, all of which were observed to be normalized at the final follow-up. Conclusions: The ocular surface disease in DEB was characterized by low corneal sensitivity, disorder of tear quality, decreased cellular cohesion, squamous metaplasia of the conjunctiva, and goblet cell loss. Close follow-up for ocular complications in DEB is essential and a pathophysiology-oriented approach to the epithelial disease may not only provide rapid healing but might prevent recurrences as well.en_US
dc.language.isoenen_US
dc.publisherLippincott Williams & Wilkinsen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectCorneal erosionen_US
dc.subjectOcular surfaceen_US
dc.subjectDystrophic epidermolysis bullosaen_US
dc.subjectVII Collagenen_US
dc.subjectDisordersen_US
dc.subjectTherapyen_US
dc.subjectExpressionen_US
dc.subjectFibronectinen_US
dc.subjectDry-eyeen_US
dc.subjectOphthalmologyen_US
dc.titleOcular surface findings in Hallopeau-Siemens subtype of dystrophic epidermolysis bullosa - Report of a case and literature reviewen_US
dc.typeArticleen_US
dc.identifier.wos000228740300019tr_TR
dc.identifier.scopus2-s2.0-17844400952tr_TR
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergitr_TR
dc.contributor.departmentUludağ Üniversitesi/Tıp Fakültesi/Göz Hastalıkları Anabilim Dalı.tr_TR
dc.identifier.startpage474tr_TR
dc.identifier.endpage479tr_TR
dc.identifier.volume24tr_TR
dc.identifier.issue4tr_TR
dc.relation.journalCorneaen_US
dc.contributor.buuauthorDoğru, Murat-
dc.relation.collaborationYurt dışıtr_TR
dc.identifier.pubmed15829808tr_TR
dc.subject.wosOphthalmologyen_US
dc.indexed.wosSCIEen_US
dc.indexed.scopusScopusen_US
dc.indexed.pubmedPubmeden_US
dc.wos.quartileQ2en_US
dc.contributor.scopusid7006540932en_US
dc.subject.scopusEpidermolysis Bullosa; Collagen Type VII; Poikiloderma of Kindleren_US
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