Case 07 - Oncology, glaucoma, and pediatric alignment

Painless Progressive Visual Field Loss

55-year-old white man - Painless progressive unilateral visual field loss - Posterior pole mass

Illustrated eye for pathology case review
Case 07Choroidal Melanoma

Clinical Presentation

This 55-year-old white man comes to your office with complaints of painless but progressive visual field loss in one eye. The accompanying photograph was taken from the affected eye.

Learner Questions

  1. When evaluating the patient's history, what questions would you ask?
  2. What diagnostic tests would you order?
  3. What would be your differential diagnosis?
  4. What treatment options would you consider?

Answer Framework

History

Prior cutaneous melanoma, family history (BAP1 syndrome, uveal melanoma), choroidal nevi, duration/progression, floaters/flashes (associated RD), weight loss/abdominal pain/jaundice (liver metastases - preferred metastatic site), prior ocular trauma/radiation.

Diagnostics

B-scan US (acoustic hollowness, choroidal excavation, orbital shadowing - measures tumor height; key test). MRI orbits (T1 hyperintense, T2 hypointense - melanin). Systemic staging: LFTs, LDH, liver MRI/US, CXR. Genetic testing: monosomy 3 + 8q amplification = high metastatic risk.

DDx

Choroidal melanoma (most common primary intraocular malignancy in adults), choroidal metastasis (breast #1 in women, lung #1 in men - overall most common intraocular malignancy), choroidal hemangioma (orange-red, posterior pole), choroidal nevus (flat, <2 mm, no SRF - ABCDE risk factors), disciform scar (AMD). Treatment Small: observation vs. TTT/plaque brachytherapy. Medium: I-125 plaque brachytherapy (COMS trial gold standard). Large: enucleation. Proton beam for posterior tumors.

Teaching Pearl

Choroidal melanoma has 50% 10-year metastatic rate regardless of treatment - liver MRI every 6-12 months for life is mandatory. Monosomy 3 on cytogenetics = highest metastatic risk. ABCDE nevus risk factors for transformation: subretinal fluid, symptoms, Diameter >5 mm, Edge touchni g disc, Orange lipofuscin pigment.

Original answer transcript
History
Prior cutaneous melanoma, family history (BAP1 syndrome, uveal melanoma), choroidal
nevi, duration/progression, floaters/flashes (associated RD), weight loss/abdominal
pain/jaundice (liver metastases - preferred metastatic site), prior ocular trauma/radiation.
Diagnostics
B-scan US (acoustic hollowness, choroidal excavation, orbital shadowing - measures
tumor height; key test). MRI orbits (T1 hyperintense, T2 hypointense - melanin). Systemic
staging: LFTs, LDH, liver MRI/US, CXR. Genetic testing: monosomy 3 + 8q amplification =
high metastatic risk.
DDx
Choroidal melanoma (most common primary intraocular malignancy in adults), choroidal
metastasis (breast #1 in women, lung #1 in men - overall most common intraocular
malignancy), choroidal hemangioma (orange-red, posterior pole), choroidal nevus (flat, <2
mm, no SRF - ABCDE risk factors), disciform scar (AMD).
Treatment
Small: observation vs. TTT/plaque brachytherapy. Medium: I-125 plaque brachytherapy
(COMS trial gold standard). Large: enucleation. Proton beam for posterior tumors.
Metastatic: liver-directed therapy. NOTE: uveal melanoma does NOT respond to
ipilimumab/checkpoint inhibitors (GNA11/GNAQ mutations, not BRAF).
TEACHING PEARL
Choroidal melanoma has 50% 10-year metastatic rate regardless of treatment - liver MRI every 6-12 months for life is mandatory. Monosomy 3 on cytogenetics =
highest metastatic risk. ABCDE nevus risk factors for transformation: subretinal fluid, symptoms, Diameter >5 mm, Edge touchni g disc, Orange lipofuscin pigment.