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Journal of pediatric ophthalmology最新文献

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Nonpulsatile exophthalmos in carotid-cavernous sinus fistula. 颈动脉海绵窦瘘无搏动性突出。
Journal of pediatric ophthalmology Pub Date : 1977-07-01 DOI: 10.3928/0191-3913-19770701-09
W. Broughton, W. Gee, J. Doppman, A. Ommaya
{"title":"Nonpulsatile exophthalmos in carotid-cavernous sinus fistula.","authors":"W. Broughton, W. Gee, J. Doppman, A. Ommaya","doi":"10.3928/0191-3913-19770701-09","DOIUrl":"https://doi.org/10.3928/0191-3913-19770701-09","url":null,"abstract":"An unusual case of carotid artery-cavernous sinus fistula with pulseless exophthalmos is presented in a two and one-half year old child. Though exophthalmos and increased episcleral venous distention were present, the ophthalmic artery pressure was not significantly altered as determined by ocular pneumoplethysmography. Consequently there was no evidence of hypoxic sequelae which frequently occur with this arteriovenous shunt. The combined use of arteriography and ocular pneumoplethysmography is advocated for determining and characterizing the presence of significant intracranial arteriovenous disease.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 4 1","pages":"221-4"},"PeriodicalIF":0.0,"publicationDate":"1977-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70103231","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 3
Arteriovenous fistula of the eyelid: secondary to a chalazion. 眼睑动静脉瘘:继发于眼睑。
Journal of pediatric ophthalmology Pub Date : 1977-07-01 DOI: 10.3928/0191-3913-19770701-10
J. Wolter
{"title":"Arteriovenous fistula of the eyelid: secondary to a chalazion.","authors":"J. Wolter","doi":"10.3928/0191-3913-19770701-10","DOIUrl":"https://doi.org/10.3928/0191-3913-19770701-10","url":null,"abstract":"An arteriovenous fistula developed on the surface of a chronic chalazion of the upper eyelid of a 21-year-old patient during pregnancy. Surgical removal of the vascular mass with ligation of the feeder arteries resulted in a complete cure.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"1 1","pages":"225-7"},"PeriodicalIF":0.0,"publicationDate":"1977-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70103240","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 6
Electron microscopic study of the orbital lesion of Hand-Schüller-Christian disease. hand - schller - christian病眼眶病变的电镜研究。
Journal of pediatric ophthalmology Pub Date : 1977-07-01
T Amemiya, H Yoshida
{"title":"Electron microscopic study of the orbital lesion of Hand-Schüller-Christian disease.","authors":"T Amemiya,&nbsp;H Yoshida","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The orbital bone lesion of a patient with Hand-Schüller-Christian disease was examined by electron microscopy. Vacuoles in the cytoplasm of foam cells contained granules which were shown by histochemical examination to be cholesterin. Langerhans cell granules in the histiocytes of Hand-Schüller-Christian disease showed a close resemblance to those in Langerhans cell of the epidermis, eosinophilic granuloma and Letterer-Siwe disease. Charcot-Leyden crystals appeared to be formed in the lysosomes of histiocytes in Hand-Schüller-Christian disease. From histopathological and cytological points of view, eosinophilic granuloma, Hand-Schüller-Christian disease and Letterer-Siwe disease are classified as histiocytosis X. The simultaneous appearance of Langerhans cell granules and Charcot-Leyden crystals is specific in histiocytosis X.</p>","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 4","pages":"242-7"},"PeriodicalIF":0.0,"publicationDate":"1977-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"11515768","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Visual acuity and binocularity in children with unilateral acquired aphakia. 单侧后天性无晶状体患儿的视力和双眼视力。
Journal of pediatric ophthalmology Pub Date : 1977-07-01 DOI: 10.3928/0191-3913-19770701-04
J. Frank, T. France
{"title":"Visual acuity and binocularity in children with unilateral acquired aphakia.","authors":"J. Frank, T. France","doi":"10.3928/0191-3913-19770701-04","DOIUrl":"https://doi.org/10.3928/0191-3913-19770701-04","url":null,"abstract":"Seventeen cases of unilateral aphakia secondary to acquired cataracts and dislocated lenses were presented. Final visual acuity was 20/70 or better in 12 of our 17 patients. Binocular single vision has been maintained in four cases. Ten patients had a posttherapy tropia. Early surgery and treatment particularly in the young child is stressed in order to maintain normal binocular single vision. Where once traumatized eyes were felt to be \"sick\" eyes and better left alone, current surgical and therapeutic methods make restoration of vision and binocularity a reasonable goal.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 4 1","pages":"200-4"},"PeriodicalIF":0.0,"publicationDate":"1977-07-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70103098","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Reaction to polyglactin 910 (Vicryl): a case report. 聚乳酸蛋白910 (Vicryl)反应1例。
Journal of pediatric ophthalmology Pub Date : 1977-05-01
A Martin-Casals, W E Scott
{"title":"Reaction to polyglactin 910 (Vicryl): a case report.","authors":"A Martin-Casals,&nbsp;W E Scott","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3","pages":"178-9"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12097499","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Subcutaneous granuloma annulare("pseudorheumatoid nodule") of the eyebrow. 眉毛皮下肉芽肿环状(“假性类风湿性结节”)。
Journal of pediatric ophthalmology Pub Date : 1977-05-01 DOI: 10.3928/0191-3913-19770501-10
A. P. Ferry
{"title":"Subcutaneous granuloma annulare(\"pseudorheumatoid nodule\") of the eyebrow.","authors":"A. P. Ferry","doi":"10.3928/0191-3913-19770501-10","DOIUrl":"https://doi.org/10.3928/0191-3913-19770501-10","url":null,"abstract":"Subcutaneous granuloma annulare occurs either as a single or multiple lesion. When the ocular adnexa are involved, the lateral aspect of the eyelid and the lateral canthus are sites of predilection. These lesions occur chiefly in children and only rarely in adults. They have the same clinical (and histopathological) appearance as rheumatoid nodules and are, therefore, also known as \"pseudorheumatoid nodules.\" Despite this similarity, these nodules are isolated lesions and are not related to systemic disease, including rheumatoid arthritis and rheumatic fever. The presently reported case exemplifies the characteristic clinical and pathological features of this disorder.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3 1","pages":"154-7"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70103109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 25
Proptosis as presenting symptom of orbital foreign body. 眼球突出是眼眶异物的主要症状。
Journal of pediatric ophthalmology Pub Date : 1977-05-01
J Scharf, S Zonis
{"title":"Proptosis as presenting symptom of orbital foreign body.","authors":"J Scharf,&nbsp;S Zonis","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>An unusual case of orbital foreign body is presented. The foreign body had penetrated through a small wound of the upper lid and was asymtomatic for two years. Proptosis due to hyperostosis of the orbital roof was a presenting symptom of the foreign body.</p>","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3","pages":"176-7"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12097497","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Mobius syndrome and limb abnormalities. 莫比乌斯综合征和肢体异常。
Journal of pediatric ophthalmology Pub Date : 1977-05-01 DOI: 10.3928/0191-3913-19770501-04
G. Rogers, G. Hatch, I. Gray
{"title":"Mobius syndrome and limb abnormalities.","authors":"G. Rogers, G. Hatch, I. Gray","doi":"10.3928/0191-3913-19770501-04","DOIUrl":"https://doi.org/10.3928/0191-3913-19770501-04","url":null,"abstract":"Most ophthalmologists are aware of the cranial nerve dysfunctions that have been associated with the facial diplegias of Mobius syndrome. However, many are not aware of the combined limb deficiencies and cranial nerve dysfunctions. Limb malformations have been associated with a spectrum of oral facial anomalies consisting of micrognathia, hypoglossia, microstomia, hypodontia, oral bands, and dysarthria. It has been suggested that the differences which exists between these entities may in fact represent a common etiology. The variability may be related to an intrauterine insult at slightly different times. The oral-facial anomalies associated with absence of limbs or of limb anomalies suggests a correlation between the limbs and the first visceral arch possibly within the second month of gestation.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3 1","pages":"134-8"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70102516","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 16
Unilateral anophthalmos and absence of right cerebral hemisphere. 单侧眼失和右脑半球缺失。
Journal of pediatric ophthalmology Pub Date : 1977-05-01 DOI: 10.3928/0191-3913-19770501-09
L. Steahly
{"title":"Unilateral anophthalmos and absence of right cerebral hemisphere.","authors":"L. Steahly","doi":"10.3928/0191-3913-19770501-09","DOIUrl":"https://doi.org/10.3928/0191-3913-19770501-09","url":null,"abstract":"A case is presented of a new eight-month-old infant with congenital anophthalmos and ipsilateral absence of cerebral tissue. Various central nervous system anomalies are described as associated with anophthalmos. Therapy is directed toward enlargement of the socket by expansion and/or surgical techniques. Early expansion therapy within the first year of life appears warranted in view of differential orbital growth rates.","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3 1","pages":"151-3"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70103052","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 1
Massive congenital ocular toxoplasmosis. 大量先天性眼弓形虫病。
Journal of pediatric ophthalmology Pub Date : 1977-05-01
F A Billson, C S Hoyt, K Hayes
{"title":"Massive congenital ocular toxoplasmosis.","authors":"F A Billson,&nbsp;C S Hoyt,&nbsp;K Hayes","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":76019,"journal":{"name":"Journal of pediatric ophthalmology","volume":"14 3","pages":"181"},"PeriodicalIF":0.0,"publicationDate":"1977-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"12097500","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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