Hereditary leiomyomatosis and renal cell cancer (Q92888): Difference between revisions
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Leiomiomatose hereditária e carcinoma de células renais (LHCCR) é uma síndrome de câncer hereditário autossômico dominante caracterizada por uma predisposição a leiomiomas cutâneos pilares, leiomiomas uterinos em mulheres e câncer de células renais. A condição está associada em até 16% dos casos a carcinoma de células renais agressivo. O diagnóstico é baseado tanto na presença de múltiplos leiomiomas cutâneos com pelo menos um leiomioma confirmado histologicamente quanto na presença de um único leiomioma com história familiar positiva para a doença. | |||
| description / en | description / en | ||
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an autosomal dominant hereditary cancer syndrome characterised by a predisposition to cutaneous pilar leiomyomata, uterine leiomyomata in women and renal cell cancer. The condition is associated in up to 16% of cases with aggressive renal cell carcinoma. Diagnosis is based on either the presence of multiple cutaneous leiomyomas with at least 1 histologically confirmed leiomyoma or the presence of a single leiomyoma with a positive family history of the disease. | |||
Revision as of 08:00, 16 August 2026
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an autosomal dominant hereditary cancer syndrome characterised by a predisposition to cutaneous pilar leiomyomata, uterine leiomyomata in women and renal cell cancer. The condition is associated in up to 16% of cases with aggressive renal cell carcinoma. Diagnosis is based on either the presence of multiple cutaneous leiomyomas with at least 1 histologically confirmed leiomyoma or the presence of a single leiomyoma with a positive family history of the disease.
| Language | Label | Description | Also known as |
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| default for all languages | ID_754002573 |
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| English | Hereditary leiomyomatosis and renal cell cancer |
Hereditary leiomyomatosis and renal cell cancer (HLRCC) is an autosomal dominant hereditary cancer syndrome characterised by a predisposition to cutaneous pilar leiomyomata, uterine leiomyomata in women and renal cell cancer. The condition is associated in up to 16% of cases with aggressive renal cell carcinoma. Diagnosis is based on either the presence of multiple cutaneous leiomyomas with at least 1 histologically confirmed leiomyoma or the presence of a single leiomyoma with a positive family history of the disease. |
