BAP1-related tumor predisposition syndrome

Orpha code: 289539OMIM code: 614327

Definition

BAP1-related tumor predisposition syndrome (TPDS) is an inherited cancer-predisposing syndrome, associated with germline mutations in BAP1 tumor suppressor gene. The most commonly observed cancer types include uveal melanoma, malignant mesothelioma, renal cell carcinoma, lung, ovarian, pancreatic, breast cancer and meningioma, with variable age of onset. Common cutaneous manifestations include malignant melanoma, basal cell carcinoma and benign melanocytic BAP1-mutated atypical intradermal tumors (MBAIT) presenting as multiple skin-coloured to reddish-brown dome-shaped to pedunculated, well-circumscribed papules with an average size of 5 mm, histologically predominantly composed of epithelioid melanocytes with abundant amphophilic cytoplasm, prominent nucleoli and large, vesicular nuclei that vary substantially in size and shape.

Disease data
Classification

Disease

Synonyms
Tumor susceptibility linked to germline BAP1 mutations
Wrażliwość na nowotwory związana z germinalnymi mutacjami BAP1
ORPHA code
289539
OMIM code
614327
ICD10 code
D23.9
ICD11 code
-

No additional description.

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