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DOI 10.1093/qjmed/hcg114

Медицинская библиотека · QJM : monthly journal of the Association of Physicians · 2003

Abdominal malignancies in patients with Wilson's disease.

Walshe J M, Waldenström E, Sams V, Nordlinder H, Westermark K

СтатьяМногоцентровое исследованиеПеревод пока не подготовлен

Аннотация

BACKGROUND

Wilson's disease is associated with heavy copper overload, primarily in the liver. Copper is a toxic metal, and might be expected to be associated with cancer induction, as iron is in haemochromatosis. However, liver cancer is currently believed to be extremely rare in this disease, and other intra-abdominal malignancies have not been reported.

AIM: To assess the frequency of abdominal malignant disease in patients with Wilson's disease on long-term follow-up.

DESIGN

Retrospective study in two specialist Wilson's disease clinics: Cambridge/London and Uppsala.

METHODS

We reviewed the case records of 363 patients seen at three centres: Addenbrooke's Hospital, Cambridge, 1955-1987; the Middlesex Hospital, London, 1987-2000; and the University Hospital, Uppsala, Sweden, 1966-2002. Patients were grouped by length of follow-up: 10-19 years; 20-29 years; 30-39 years; and 40 years or more.

RESULTS

No cancers were seen in patients followed for <10 years. For patients in the 10-19 years group, the frequency was 4.2%; at 20-29 years, it was 5.3%; and at 30-39 years, 15%. No cancers were seen in the 40+ years follow-up group. The cancers consisted of hepatomas, cholangiocarcinomas, and poorly differentiated adenocarcinomas of undetermined primary site.

DISCUSSION: Patients with Wilson's disease appear to be vulnerable to the formation of aggressive malignant intra-abdominal tumours during long-term follow-up, irrespective of treatment. Ultrasound scanning of the abdomen seems to be a useful screening procedure.

Для цитирования: Walshe J M, Waldenström E, Sams V, Nordlinder H, Westermark K. Abdominal malignancies in patients with Wilson's disease.. QJM : monthly journal of the Association of Physicians. 2003. DOI: 10.1093/qjmed/hcg114.

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