scholarly journals Isolated Ocular Sarcoidosis Mimicking Ring Melanoma

2019 ◽  
Vol 6 (3) ◽  
pp. 180-183
Author(s):  
Carsten Faber ◽  
Rasmus Ejstrup ◽  
Karine Madsen ◽  
Steffen Heegaard ◽  
David Scheie ◽  
...  

We report the case of a 25-year-old female, who presented with a large, pale tumor of her ciliary body that extended to >180° of the anterior chamber angle. All preoperative examinations including ultrasound biomicroscopy, scleral transillumination, and MRI indicated melanoma. A thorough systemic work-up was negative. A diagnosis of ring melanoma was suspected, and the patient was scheduled for enucleation. However, perioperative frozen section indicated granulomatous inflammation. The enucleation was cancelled, and a subtenon injection of triamcinolone was administered, which resulted in the disappearance of the tumor. Together, the findings meet the criteria for the diagnosis of isolated ocular sarcoidosis. This case demonstrates that a sarcoid granuloma can mimic all clinical features of a ring melanoma. Therefore, a biopsy should be done before destructive surgery is carried out.

2021 ◽  
pp. 403-410
Author(s):  
Mina M. Naguib ◽  
Patricia Chévez-Barrios ◽  
Silvia Orengo-Nania ◽  
Amy C. Schefler

We report the clinical history and histopathological findings in a case of diffuse iris ring melanoma (DIM) and review the most recent literature and modern molecular genetics of this entity. An 85-year-old Hispanic man presented with severe unilateral glaucoma, managed at an outside institution for 2 years prior to presentation. Diffuse pigmentation was noted in the angle, on the intraocular lens implant, and in the vitreous without clear demonstration of a mass on ultrasound biomicroscopy. Workup for metastatic cutaneous melanoma was negative. Histopathological examination of the enucleated eye revealed a mixed cell type iris ring melanoma with diffuse intraocular involvement. Gene expression profiling (GEP) revealed a class 2 molecular signature indicating a very high risk for metastases. Unilateral glaucoma presenting with marked pigmentation in the anterior chamber angle should be managed as melanoma until proven otherwise. Iris ring melanomas are known to have an aggressive clinical course, and recent molecular analyses indicate that they are likely primarily GEP class 2 with a very poor prognosis, similar to the majority of ciliary body melanomas.


2020 ◽  
Vol 20 (1) ◽  
Author(s):  
Jingli Guo ◽  
Wenyi Tang ◽  
Wei Liu ◽  
Min Zhou ◽  
Qing Chang ◽  
...  

Abstract Background To report undescribed characteristics of patients with bilateral diffuse uveal melanocytic proliferation (BDUMP) on ultrasound biomicroscopy (UBM) and high-frequency B-scan ultrasonography. Case presentation Two of four participants presented with worsening bilateral vision after previously diagnosed primary pulmonary or ovarian carcinoma. The other two patients were diagnosed with lung carcinoma after presentation with BDUMP. All patients had ciliary body nevi-like lesion in combination with iris or ciliary body cysts, and uveal thickening on UBM. Focally elevated choroidal nevi-like lesion and exudative retinal detachment with choroidal thickening were detected with B-scan ultrasonography. Conclusions Our case series demonstrates the uveal characteristics of patients with BDUMP based on high-frequency B-scan ultrasonography and UBM. Ultrasonographic findings are crucial in the diagnosis of BDUMP because it is occult in nature.


2017 ◽  
Vol 255 (12) ◽  
pp. 2437-2442 ◽  
Author(s):  
Yoshifumi Okamoto ◽  
Fumiki Okamoto ◽  
Shinichiro Nakano ◽  
Tetsuro Oshika

2019 ◽  
Vol 12 (6) ◽  
pp. e229397
Author(s):  
Samendra Karkhur ◽  
Alok Sen ◽  
Gautam Parmar ◽  
Priyavrat Bhatia

A 32-year-old man presented with bilateral diminution of vision for 10 years. Visual acuity was light perception in both eyes with inaccurate projection in the oculus dextrus(OD) and accurate projection in the in oculus sinister (OS). Intraocular pressure was 6 and 12 mm Hg in the OD and OS, respectively. Slit-lamp examination revealed the presence of leucomatous corneal opacification with microcornea in oculus uterque (OU). Both eyes had a dislocated nucleus in the vitreous cavity on ultrasound B-scan with advanced cupping in the right eye. Ultrasound biomicroscopy revealed ciliary body atrophy in the OD and preserved ciliary processes (two quadrants) in the OS. In view of a partially preserved ciliary body function and a potential for gaining useful vision, we planned surgical intervention in the left eye. Deep anterior lamellar keratoplasty with pars planavitrectomy (PPV) and phacofragmentation of the nucleus was done. Donor lamellar graft was sutured after completion of PPV and nucleus fragmentation. The patient regained useful ambulatory vision postoperatively with clear corneal graft.


2020 ◽  
pp. 112067212092022
Author(s):  
Harathy Selvan ◽  
Seema Kashyap ◽  
Seema Sen ◽  
Bhavna Chawla ◽  
Neiwete Lomi ◽  
...  

Extramedullary plasmacytoma of the iris and ciliary body is extremely rare. We present a case which was misdiagnosed as granulomatous uveitis with neovascular glaucoma, and underwent a trabeculectomy with mitomycin-c along with iris biopsy. The post-operative period showed early bleb failure and catastrophic growth of the suspected mass. Histopathological examination revealed a diagnosis iris plasmacytoma. Subsequent ultrasound biomicroscopy showed involvement of the iris and ciliary body. A prompt systemic workup was done, and an associated systemic plasma cell dyscrasia was ruled out. The affected eye was enucleated, and the patient remains disease free at the end of 3-year follow-up.


2014 ◽  
Vol 23 (2) ◽  
pp. 61-68 ◽  
Author(s):  
Zhong Lin ◽  
Da P. Mou ◽  
Yuan B. Liang ◽  
Si Z. Li ◽  
Rui Zhang ◽  
...  

2013 ◽  
Vol 155 (4) ◽  
pp. 681-687.e2 ◽  
Author(s):  
Juan P. Velazquez-Martin ◽  
Hatem Krema ◽  
Emiliano Fulda ◽  
Yeni H. Yücel ◽  
E. Rand Simpson ◽  
...  

1985 ◽  
Vol 69 (7) ◽  
pp. 514-518 ◽  
Author(s):  
W Omulecki ◽  
M Pruszczynski ◽  
J Borowski
Keyword(s):  

Sign in / Sign up

Export Citation Format

Share Document