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Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery最新文献

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Subperiosteal abscess of the orbit with multiple abscesses in the brain and body due to Chromobacterium violaceum sepsis in an infant: a case report and review of the literature.
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-12 DOI: 10.1080/01676830.2025.2462623
Uprimporn Suthiwong, Patcharaporn Chandraparnik
{"title":"Subperiosteal abscess of the orbit with multiple abscesses in the brain and body due to <i>Chromobacterium violaceum</i> sepsis in an infant: a case report and review of the literature.","authors":"Uprimporn Suthiwong, Patcharaporn Chandraparnik","doi":"10.1080/01676830.2025.2462623","DOIUrl":"https://doi.org/10.1080/01676830.2025.2462623","url":null,"abstract":"<p><p><i>Chromobacterium violaceum</i> is a rare pathogen known to cause severe, life-threatening infections in humans. Its typical clinical presentations include skin and soft tissue infections, fulminant septicemia, multiple visceral abscesses, and diarrhea. We report the case of a 2-month-old male infant who initially presented with acute fever and subsequently developed acute proptosis of the right eye, accompanied by a palpable mass in the right mastoid area. Computed tomography (CT) scans of the orbits, paranasal sinuses and brain revealed a subperiosteal abscess at the right sphenoid wing, right otomastoiditis, and multiple intracerebral abscesses. Moreover, ultrasonography of the whole abdomen showed multiple liver abscesses. Blood culture analysis confirmed the presence of <i>Chromobacterium violaceum</i>, while comprehensive testing for underlying immunodeficiency returned negative results. The patient's condition was effectively managed through timely surgical intervention, including lateral orbitotomy for pus drainage, combined with appropriate antibiotic treatment. After completing the prescribed course of prophylactic antibiotics, the patient remained free from disease recurrence and showed sustained clinical recovery.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"1-4"},"PeriodicalIF":0.9,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143400335","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
Role of biomarkers in South Indian Thyroid Eye Disease study (SITED).
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-12 DOI: 10.1080/01676830.2025.2453536
Pratheeba Devi Nivean, Rohit Shetty, Swaminathan Sethu, Arkasubhra Ghosh, Govindasamy Kumaramanikavel, Keerti Koka, Carroll A B Webers, Tos Tjm Berendschot, Dion Paridaens
{"title":"Role of biomarkers in South Indian Thyroid Eye Disease study (SITED).","authors":"Pratheeba Devi Nivean, Rohit Shetty, Swaminathan Sethu, Arkasubhra Ghosh, Govindasamy Kumaramanikavel, Keerti Koka, Carroll A B Webers, Tos Tjm Berendschot, Dion Paridaens","doi":"10.1080/01676830.2025.2453536","DOIUrl":"https://doi.org/10.1080/01676830.2025.2453536","url":null,"abstract":"<p><strong>Purpose: </strong>Thyroid eye disease (TED) is a complex autoimmune disease. Early detection with routine disease monitoring using biomarker assessment would help in mitigating TED-associated vision loss. Hence, we performed a non-invasive tear fluid (TF) based screening in patients with TED as part of the South Indian Thyroid Eye Disease Study (SITED).</p><p><strong>Materials and methods: </strong>We used TF from healthy controls (HC;13 eyes;13 subjects), patients with thyroid dysfunction but without TED (No TED;11 eyes;11 subjects) and patients with TED (18 eyes;18 subjects). TED subjects were further sub-divided into those with and without an active form of the disease. Patients with dysthyroid optic neuropathy (DON) were analyzed separately. The diagnosis of TED was based on Gorman and Bartley's criteria. Activity was defined as scoring more than 4 in the Vision, Inflammation, Strabismus and Appearance (VISA). Schirmer's strip was used to collect TF and the levels of IL-2, IL-4, IL-5, IL-6, IL-7, IL-9, IL-10, IL-13, IL-17A, IL-17F, IL-22, IFNγ, TNFα, PDGF-AA and PDGF-BB were determined by multiplex ELISA using flow cytometry.</p><p><strong>Results: </strong>Significantly (<i>p</i> < 0.05) higher levels of IL-6 and IL-10 were observed in TED patients compared to HC and No TED subjects. TF levels of IL-6 and IL-10 were significantly higher in active TED patients compared to No TED subjects. Interestingly, TF levels of PDGF-AA were observed to be negatively associated with IL-4 and IL-13.</p><p><strong>Conclusion: </strong>Elevated TF levels of IL-6 and IL-10 can be explored for their role as a non-invasive risk stratification biomarker or as targets to modulate management of TED.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"1-9"},"PeriodicalIF":0.9,"publicationDate":"2025-02-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143400329","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
Thyroid autoantibodies in paediatric thyroid eye disease patients in an Australian population.
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-05 DOI: 10.1080/01676830.2025.2457595
Delia D Wang, Timothy J Sullivan
{"title":"Thyroid autoantibodies in paediatric thyroid eye disease patients in an Australian population.","authors":"Delia D Wang, Timothy J Sullivan","doi":"10.1080/01676830.2025.2457595","DOIUrl":"https://doi.org/10.1080/01676830.2025.2457595","url":null,"abstract":"<p><strong>Purpose: </strong>This study presents the clinical features and management of paediatric TED patients in an Australian population, together with the longitudinal trend of TRAb and TSI over time.</p><p><strong>Methods: </strong>A retrospective case series study was conducted on patients with paediatric TED between 2003 and 2023. A comprehensive dataset was collected and analysed for each case, encompassing patient demographics, clinical features and management of their TED, as well as their thyroid antibody levels over the study period.</p><p><strong>Results: </strong>Thirty-four patients were included, with a female preponderance. The age at diagnosis of thyroid dysfunction (mean age 12.1 years, range 3-17 years, SD ± 3.6 years) tended to slightly precede the age at diagnosis of TED (mean age 12.7 years, range 3-17 years, SD ± 3.59 years). The most common main TED symptom at presentation was prominent eyes in 25 patients (73.5%), and the most common presenting sign of TED was proptosis in 32 patients (94%). No patients had dysthyroid optic neuropathy. The majority (88%) of our paediatric TED patients had mild disease with a mean presenting VISA score of 1.76, and a CAS score of 1.71. During the follow up period, the average peak TRAb reached 44.2 IU/L (SD ± 96.94 IU/L), and over an average time period of 42.4 months, the most recent average TRAb level settled to 6.6 IU/L (SD ± 7.76 IU/L). The TSI levels also followed a downward trend over time.</p><p><strong>Conclusions: </strong>Paediatric TED is rarer than adult TED with milder clinical presentations. TRAb and TSI levels in paediatric TED patients tend to follow the disease course, with a downward trend over time.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"1-9"},"PeriodicalIF":0.9,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143190905","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
Response to comments on "ChatGPT and frequently asked patient questions for upper eyelid blepharoplasty surgery". 对 "ChatGPT 和上眼睑眼睑整形手术患者常见问题 "评论的回复。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-05 DOI: 10.1080/01676830.2025.2458674
Michelle M Maeng, Phillip A Tenzel
{"title":"Response to comments on \"ChatGPT and frequently asked patient questions for upper eyelid blepharoplasty surgery\".","authors":"Michelle M Maeng, Phillip A Tenzel","doi":"10.1080/01676830.2025.2458674","DOIUrl":"https://doi.org/10.1080/01676830.2025.2458674","url":null,"abstract":"","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"1-2"},"PeriodicalIF":0.9,"publicationDate":"2025-02-05","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143190902","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
Sarcoid-like reaction of the orbit in diffuse large B-cell lymphoma. 弥漫大 B 细胞淋巴瘤眼眶肉样瘤样反应。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-03-05 DOI: 10.1080/01676830.2024.2318765
Frank Mei, Snehaa Maripudi, Robert N Hogan, Jennifer Cao, Ronald Mancini
{"title":"Sarcoid-like reaction of the orbit in diffuse large B-cell lymphoma.","authors":"Frank Mei, Snehaa Maripudi, Robert N Hogan, Jennifer Cao, Ronald Mancini","doi":"10.1080/01676830.2024.2318765","DOIUrl":"10.1080/01676830.2024.2318765","url":null,"abstract":"<p><p>Sarcoid-like reaction (SLR) has been reported in patients with solid tumor malignancies, lymphomas, and patients receiving immunotherapy. SLR is often incidentally found during positron emission tomography/computed tomography scans as hilar and/or mediastinal lymphadenopathy. SLR has also been found in the lung, spleen, bone marrow, and skin. Biopsy of these lesions shows noncaseating granulomas. When systemic criteria are not met for sarcoidosis, these noncaseating granulomas are termed SLR. We present the first case in the literature of a case of orbital SLR in a patient with concomitant diffuse large B-cell lymphoma and inverted papilloma of the maxillary sinus. This case highlights the importance of including malignancy in the differential for the presence of a noncaseating granuloma in the orbit.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"104-107"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140029309","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
Dilemmas in the management of lacrimal drainage anomalies in BOSMA (congenital arhinia-microphthalmia) syndrome. BOSMA（先天性泪小管综合症）泪道引流异常的治疗难题。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-05-07 DOI: 10.1080/01676830.2024.2346568
Meghana Anika Varde, Mohammad Javed Ali
{"title":"Dilemmas in the management of lacrimal drainage anomalies in BOSMA (congenital arhinia-microphthalmia) syndrome.","authors":"Meghana Anika Varde, Mohammad Javed Ali","doi":"10.1080/01676830.2024.2346568","DOIUrl":"10.1080/01676830.2024.2346568","url":null,"abstract":"<p><p>Congenital arhinia-microphthalmos syndrome or BOSMA syndrome is an exceptionally rare clinical syndrome characterized by unilateral or bilateral complete absence of the nasal cavity associated with several craniofacial, ocular, and systemic anomalies. Lacrimal drainage anomalies are secondary to absent nasolacrimal duct and usually present as dilated lacrimal sac or mucoceles. While navigation-guided dacryocystorhinostomies into the contralateral nasal cavity are described for unilateral arhinia, the way forward for the complete absence of the nose and nasal cavity is still unclear. A multidisciplinary team from the specialties of genetics, plastic surgery, ophthalmic plastics and reconstructive surgery, otorhinolaryngology, and endocrinology should get involved very early on for better continuity of care.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"121-124"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140877648","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
Resolution of Pityriasis rubra pilaris induced ectropion with oral dexamethasone. A case report. 口服地塞米松治疗红斑狼疮引起的外翻。病例报告。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-02-06 DOI: 10.1080/01676830.2024.2311657
Ourania Fydanaki, Haytham Rezq, Anastasios E Sepetis, Varajini Joganathan
{"title":"Resolution of Pityriasis rubra pilaris induced ectropion with oral dexamethasone. A case report.","authors":"Ourania Fydanaki, Haytham Rezq, Anastasios E Sepetis, Varajini Joganathan","doi":"10.1080/01676830.2024.2311657","DOIUrl":"10.1080/01676830.2024.2311657","url":null,"abstract":"<p><p>An 82-year-old male presented with generalised Pityriasis rubra pilaris (PRP) managed initially by dermatology team. The patient did not respond to first- and second-line treatment, including oral acitretin, steroid creams, and methotrexate, and developed bilateral cicatricial ectropion, for which he was referred to oculoplastic team for surgical management. A head injury resulting in subacute subdural haematoma, managed with a week course of low dose oral dexamethasone, resulted in the improvement of his skin condition and complete resolution of the cicatricial ectropion within a few weeks. Thus, systemic treatment of PRP with oral dexamethasone may be considered sooner in the treatment of cicatricial ectropion in similar cases.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"87-89"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139693207","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
A case of disseminated nocardiosis with orbital apex involvement and endophthalmitis. 一例伴有眼眶顶受累和眼底炎的播散性诺卡菌病。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-04-22 DOI: 10.1080/01676830.2024.2343302
Reema Madike, Khizar Rana, Sandy Patel, Dinesh Selva
{"title":"A case of disseminated nocardiosis with orbital apex involvement and endophthalmitis.","authors":"Reema Madike, Khizar Rana, Sandy Patel, Dinesh Selva","doi":"10.1080/01676830.2024.2343302","DOIUrl":"10.1080/01676830.2024.2343302","url":null,"abstract":"<p><p>Nocardia is a rare cause of ocular infections and most commonly occurs secondary to trauma. Systemic Nocardiosis may have ocular involvement in rare cases. We report a case of disseminated nocardiosis with orbital apex involvement and endophthalmitis in an immunocompromised patient. The patient presented with respiratory sepsis, and later developed complete ptosis and ophthalmoplegia in the left eye. This was on the background of treatment with high-dose prednisolone. Magnetic resonance imaging showed enhancement of the entire clivus, extending into the left orbital apex and cavernous sinus. The patient was initially treated empirically for CNS tuberculosis. Bronchoscopic cultures returned positive for Nocardia farcinica, and the patient was treated with trimethoprim/sulfamethoxazole and weaned off previous corticosteroids.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"117-120"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140871970","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
Lambda-double-fixation for medial epicanthoplasty in Blepharophimosis - Ptosis - Epicanthus Inversus Syndrome. 眼睑下垂-上睑下垂-上睑下垂综合征的内侧上睑下垂成形术中的 Lambda 双固定术。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-03-21 DOI: 10.1080/01676830.2024.2328259
Ramón Medel, Elena Scherrer, Lucía Castaño Fernández-Vega, Juan Ignacio Racana, Claudia Cordero, María Inmaculada Paños Palacios, Luz Maria Vasquez
{"title":"Lambda-double-fixation for medial epicanthoplasty in Blepharophimosis - Ptosis - Epicanthus Inversus Syndrome.","authors":"Ramón Medel, Elena Scherrer, Lucía Castaño Fernández-Vega, Juan Ignacio Racana, Claudia Cordero, María Inmaculada Paños Palacios, Luz Maria Vasquez","doi":"10.1080/01676830.2024.2328259","DOIUrl":"10.1080/01676830.2024.2328259","url":null,"abstract":"<p><strong>Purpose: </strong>This study aims to describe a novel approach to medial epicanthoplasty in patients with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and evaluate the surgical outcome of this technique.</p><p><strong>Methods: </strong>A retrospective, noncomparative, interventional case series involving 22 BPES patients who underwent medial epicanthoplasty using the Lambda-Double-Fixation technique (LDFT) performed by a single surgeon. Pre- and postoperative measurements of inner intercanthal distance (DIC) and horizontal palpebral fissure (HPFL) were recorded. Concurrent or staged ptosis surgery and lateral cantholysis, along with any complications, were documented.</p><p><strong>Results: </strong>The mean age of the patients was 2.9 ± 2.2 years. Preoperatively, the mean DIC measured 34.0 ± 2.7 mm, significantly reducing to 23.7 ± 2.1 mm postoperatively (<i>p</i> < 0.001). A notable increase in mean HPFL was observed in both eyes postoperatively: right eye form 18.4 ± 2.4 mm to 23.7 ± 1.8 mm (<i>p</i> < 0.001) and left eye from 18.3 ± 2.4 mm to 23.8 ± 1.9 mm (<i>p</i> < 0.001). Postoperative scars were barely visible in all patients.</p><p><strong>Conclusion: </strong>LDFT is a simple and reproducible technique for medial epicanthoplasty in BPES. Our results affirm that LDFT induces a physiologically concave reshaping of the medial canthal region, optimizing access to the peritarsal zone and ensuring a secure fixation of the new canthus. These benefits lead to a reduction in ICD and an increase in HPFL, leading to a cosmetically appealing postoperative outcome.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"64-70"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140177136","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
Orbital invasion of a conjunctival atypical fibroxanthoma in a patient with systemic diffuse large B-cell lymphoma. 一名全身弥漫大 B 细胞淋巴瘤患者的结膜非典型纤维黄瘤侵犯眼眶。
IF 0.9
Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery Pub Date : 2025-02-01 Epub Date: 2024-05-26 DOI: 10.1080/01676830.2024.2350041
Márcia Cristina Todo, Julie Anne Gonçalves de Carvalho, Juliana Bisco Ferreira da Silveira E Freitas, Luís Sérgio Grecca, Fernando Chahud, Antônio Augusto Velasco E Cruz
{"title":"Orbital invasion of a conjunctival atypical fibroxanthoma in a patient with systemic diffuse large B-cell lymphoma.","authors":"Márcia Cristina Todo, Julie Anne Gonçalves de Carvalho, Juliana Bisco Ferreira da Silveira E Freitas, Luís Sérgio Grecca, Fernando Chahud, Antônio Augusto Velasco E Cruz","doi":"10.1080/01676830.2024.2350041","DOIUrl":"10.1080/01676830.2024.2350041","url":null,"abstract":"<p><p>An 88-year-old male patient presented with a large mass on the left lateral bulbar conjunctiva. The tumor appeared two months after the resection of a conjunctival atypical fibroxanthoma (AFX) performed by a cornea specialist. Magnetic resonance imaging of the orbits showed deep orbital invasion along the lateral rectus muscle. The mass and the entire conjunctival sac were totally excised with lid-sparing orbital exenteration. Histopathological analysis confirmed that the mass was an extension of the AFX. Two weeks after surgery, large B-cell lymphoma was diagnosed in the oropharynx. Chemotherapy was initiated, and after seven months of follow-up, there was no recurrence of the AFX. The authors believe that this is the first report of orbital invasion by AFX.</p>","PeriodicalId":47421,"journal":{"name":"Orbit-The International Journal on Orbital Disorders-Oculoplastic and Lacrimal Surgery","volume":" ","pages":"125-128"},"PeriodicalIF":0.9,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141155655","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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