Enteropathy associated T cell lymphoma presenting as an isolated CNS lymphoma three years after diagnosis of coeliac disease: T cell receptor polymerase chain reaction studies failed to show the original enteropathy to be a clonal disorder

• Published in: Gut 1997-06, Vol.40 (6), p.801-803
• Main Authors: Tutt, A N, Brada, M, Sampson, S A
• Format: Article
• Language: English
• Subjects: Biological and medical sciences; Brain Neoplasms - diagnostic imaging; Brain Neoplasms - etiology; Celiac Disease - complications; Female; Gastroenterology. Liver. Pancreas. Abdomen; Hematologic and hematopoietic diseases; Humans; Leukemias. Malignant lymphomas. Malignant reticulosis. Myelofibrosis; Lymphoma, T-Cell - diagnostic imaging; Lymphoma, T-Cell - etiology; Medical sciences; Middle Aged; Other diseases. Semiology; Polymerase Chain Reaction; Receptors, Antigen, T-Cell - analysis; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus; Tomography, X-Ray Computed
• ISSN: 0017-5749; 1468-3288; 1458-3288
• DOI: 10.1136/gut.40.6.801

A case of enteropathy associated T cell lymphoma is reported in a 45 year old woman, presenting with isolated disease in the CNS, three years after diagnosis of coeliac disease. Initial staging showed no evidence of gastrointestinal tract lymphoma. A presumptive diagnosis of T cell primary cerebral lymphoma was made and the patient was treated with combination chemotherapy and craniospinal radiotherapy. The patient relapsed, seven months after treatment, with small bowel lymphoma. The immunophenotype and T cell receptor polymerase chain reaction analysis confirmed the same tumour as in the CNS. Retrospective polymerase chain reaction analysis of intraepithelial lymphocytes in the duodenal biopsy sample, taken at the time of diagnosis of coeliac disease, failed to show evidence of a clonal T cell proliferation.