scholarly journals Lagophthalmos of the upper eyelid after rhinoplasty: A case report

2021 ◽  
Vol 9 (9) ◽  
Author(s):  
Hesam Jahandideh ◽  
Fatemeh Dehghani Firouzabadi ◽  
Mohammad Dehghani Firouzabadi ◽  
Maryam Roomiani
Keyword(s):  
2011 ◽  
Vol 35 (2) ◽  
pp. 181-183
Author(s):  
Georgios Koulaxouzidis ◽  
Steffen Eisenhardt ◽  
Vincenzo Penna ◽  
Holger Bannasch ◽  
Nestor Torio-Padron

2000 ◽  
Vol 10 (2) ◽  
pp. 173-176 ◽  
Author(s):  
L. Collaço ◽  
J.P. Silva ◽  
M. Gonçalves ◽  
P. Abrantes

A 22-year-old woman who presented with a tumour of the upper eyelid with clinical, histological, immunohistochemical and ultrastructural features of a Merkel cell carcinoma is reported. This is a unique case of Merkel cell carcinoma in such a young patient. This neuroendocrine tumour is typically found in the elderly. It can grow rapidly, has the potential for local recurrence and early metastatic spread. The authors recommend wide resection of the primary site, which proved effective in this case.


Author(s):  
Suppapong Tirakunwichcha ◽  
Lalana Sansopha ◽  
Chaturong Putaporntip ◽  
Somchai Jongwutiwes

A 59-year-old female living in Rayong Province, eastern Thailand, presented with painless, right upper eyelid nodule for 3 months. Upon removal of the eyelid mass, a well-circumscribed, firm globular mass with diameter about 1 cm was found. Histopathological examination revealed an immature female dirofilarial worm reminiscent of Dirofilaria repens, characterized by prominent sharp longitudinal ridges at external surface of the cuticle. Analysis of the mitochondrial 12S rRNA sequence showed that the worm belongs to Candidatus Dirofilaria hongkongensis. It is likely that some infections previously reported as D. repens based on histological examination may have actually been due to Candidatus D. hongkongensis.


2019 ◽  
Vol 56 (10) ◽  
pp. 1377-1380
Author(s):  
Joshua M. Barnett ◽  
John H. Y. Pang ◽  
Sean Herman ◽  
Jonathan Lee ◽  
S. Tonya Stefko ◽  
...  

Objective: To describe a reliable method utilizing large, rotation flaps to reconstruct a number 10 Tessier cleft. Design: This is a descriptive clinical case report. Setting: Pediatric teaching hospital affiliated with a university. Patients, Participants: One participant in this clinical case report. Interventions: Full-thickness excision of the clefted eyelid, brow, and forehead tissue was performed bilaterally to develop medial and lateral eyebrow and forehead flaps. Right: the forehead/brow flap was rotated caudally to reapproximate the eyebrow and an eyelid rotation flap was also used to reapproximate the lid margin. Left: forehead/brow rotation flap allowed realignment of the eyebrow and a series of Z-plasties were used in the eyelid to reapproximate the lid margin and to lengthen the eyelid. Main Outcome Measure(s): Develop and construct a reliable reconstruction with full-eyelid closure and minimal donor site morbidity. Results: Complete eyelid closure bilaterally was achieved intraoperatively, and was maintained at 6-month follow-up with no evidence of ocular pathology. Conclusions: Large, bilateral upper eyelid colobomas require repair to prevent blindness. Although free tarsomarginal grafts and lid-sharing procedures have been described, we demonstrate that large rotation flaps designed along the cleft margin can provide a reliable reconstruction and minimize donor-site morbidity.


2009 ◽  
Vol 23 (4) ◽  
pp. 301 ◽  
Author(s):  
Ju Hyang Lee ◽  
Yong Woon Shin ◽  
Young Ha Oh ◽  
Yoon Jung Lee
Keyword(s):  

1999 ◽  
Vol 43 (2) ◽  
pp. 215-217 ◽  
Author(s):  
Daichi Morioka ◽  
Yoshio Kinoshita ◽  
Tsuyoshi Tanabe ◽  
Yoshimichi Ueda

2015 ◽  
Vol 8 (1) ◽  
pp. 56 ◽  
Author(s):  
RehabMonir Samaka ◽  
Ali Al-Madhani ◽  
ShereenOssman Hussian

Orbit ◽  
1999 ◽  
Vol 18 (1) ◽  
pp. 53-58 ◽  
Author(s):  
Sabrina D. Shah-Desai ◽  
Amanda L. Collins ◽  
A.G. Tyers

2010 ◽  
Vol 13 (1) ◽  
pp. 35-37
Author(s):  
F Nasiri ◽  
F Mahjoubi ◽  
G Babamohammadi

De Novo Duplication of Chromosome 7 (q21.1-q32); Case Report and Review of the LiteratureCytogenetic analysis of a 1-year-old boy with multiple congenital anomalies revealed partial duplication of the chromosome 7q21.2-q32 band region. His main features included: frontal bossing, small jaw, low-set ears, deep-set eyes, strabismus, drooping left upper eyelid, widely-spaced eyes, short nose, long philtrum, down-curved upper lip, camptodactyly and hypotonia.


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