Primary orbital synovial sarcoma: a clinicopathologic review with a differential diagnosis and discussion of molecular genetics
AM Stagner, FA Jakobiec, A Fay - Survey of Ophthalmology, 2017 - Elsevier
Synovial sarcoma is a soft-tissue sarcoma of the extremities developing in young adults that
has rarely been reported in the orbit. Synovial sarcoma is associated with a unique …
has rarely been reported in the orbit. Synovial sarcoma is associated with a unique …
Isolated neurofibroma of the orbit: case report and literature review
PS Braich, JC Donaldson, GS Bajaj… - Ophthalmic Plastic & …, 2018 - journals.lww.com
Purpose: To summarize the clinical, radiographic, and intraoperative characteristics of
isolated neurofibromas of the orbit (INFO) in the literature and report a case of INFO …
isolated neurofibromas of the orbit (INFO) in the literature and report a case of INFO …
Intraocular medulloepitheliomas and embryonal tumors with multilayered rosettes of the brain: comparative roles of LIN28A and C19MC
Purpose To compare immunohistochemical and genetic overlaps and differences between
intraocular medulloepitheliomas and embryonal tumors with multilayered rosettes of the …
intraocular medulloepitheliomas and embryonal tumors with multilayered rosettes of the …
Dermatofibroma of the eyelid with monster cells
FA Jakobiec, Y Tu, FR Zakka, AKF Tong - Survey of Ophthalmology, 2017 - Elsevier
Dermatofibromas are most frequently encountered in women on the lower extremities, often
after minor trauma. A recurrent lesion of the right lower eyelid developed in a 64-year-old …
after minor trauma. A recurrent lesion of the right lower eyelid developed in a 64-year-old …
[HTML][HTML] Orbital myxoma: a case report
L Weisbrod, K Smith, P Camarata… - Surgical neurology …, 2020 - ncbi.nlm.nih.gov
Background: Myxomas are rare, locally infiltrative, benign neoplasms of mesenchymal
origin. Although benign, these tumors are locally aggressive with a high rate of recurrence …
origin. Although benign, these tumors are locally aggressive with a high rate of recurrence …
Myxoma: An Unusual Aggressive Orbital Lesion
C Quigley, JY Tong, G Farshid, F Bonar… - Ophthalmic Plastic & …, 2024 - journals.lww.com
Myxoma is a rare tumor that can be challenging to diagnose, with imaging findings that can
be nonspecific. We present a case of a 21-year-old man who presented with a subacute …
be nonspecific. We present a case of a 21-year-old man who presented with a subacute …
Isolated intraosseous extra-gnathic orbital myxoma: a clinicopathologic case report
FP Manjandavida, S Chahar, B Dave - Orbit, 2019 - Taylor & Francis
ABSTRACT A 19-year-old female student presented with painless, progressive proptosis in
the right eye for the past six months causing significant cosmetic blemish and double vision …
the right eye for the past six months causing significant cosmetic blemish and double vision …
Aggressive Angiomyxoma of Ear
Aggressive angiomyxoma (AA) is an extremely rare, locally invasive, mesenchymal tumor. It
has a high propensity of recurrence and rapid growth, especially if complete excision of the …
has a high propensity of recurrence and rapid growth, especially if complete excision of the …
Small benign storiform fibrous tumor (fibrous histiocytoma) of the conjunctival substantia propria in a child: review and clarification of biologic behavior
MG Tieger, FA Jakobiec, L Ma… - Ophthalmic Plastic & …, 2019 - journals.lww.com
Purpose: A case of a small benign storiform fibrous tumor of the conjunctival substantia
propria is described to clarify the category of fibrous histiocytoma. In addition, a comparison …
propria is described to clarify the category of fibrous histiocytoma. In addition, a comparison …
Primary intraocular malignant rhabdoid tumor without extrascleral compromise
E Ayala Barroso, A Tapia Bahamondes… - Journal of Pediatric …, 2018 - journals.healio.com
Primary intraocular malignant rhabdoid tumor is classified as a malignant extrarenal
rhabdoid tumor. It is extremely rare, highly aggressive, and, so far, only one case (in a …
rhabdoid tumor. It is extremely rare, highly aggressive, and, so far, only one case (in a …