《Slide 97.》Malignant melanoma, Eye
A. Brief Descriptions:
Arising from pigmented neuroepithelia or
uveal melanocytes.
Most common in
posterior choroid in eye.
B. Gross Findings:
Apple & Blodi classification
Obvious and unquestionable nevi and melanocytoma
Phase A tumor:
Relatively small, not extended or metastatic beyond eye
Most cells classified toward benign end and stationary or slow growing
Phase B tumor:
Large, extensive and rapid growth with malignant bizarre cells
Callender classification
Spindle A and spindle B cell groups
Slender, elongated, spindle shape, cohesive cells
With poorly visualized cell border
Slender, elongated, spindle shaped nuclei
Spindle A cells : devoid of nucleolus
Spindle B cells : larger, with prominent nucleoli
Fascicular: cells in parallel rows, bundles about dilated vessels, with palisading nuclei
Mixed spindle and epithelioid cells
Epithelioid cells:
Larger cells variation in size and shape
Well-demarcated, poorly cohesive
Abundant cytoplasm, hyperchromatic nucleus with prominent nucleoli
Frequent mitosis
Multinucleated tumor giant cells
C. Micro Findings:
Tumor grows into
vitrous cavity with elevated retinal layer with dark-brown
melanin pigments.
Epithelioid cells with large cell size, abundant cytoplasm,
hyperchromatic nuclei
and prominent
nucleoli.
Layer of spindle cells, some with prominent nucleoli.
D. Others:
Arising from pigmented neuroepithelia or uveal melanocyte
Most common in posterior choroid in eye
E. Reference:
Robbins pathologic basis of disease.
Ch31. p.1366-1367.
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