Leptomeningitis as Rare Secondary Dissemination in MEITL (Monomorphic Intestinal Epitheliotropic T-Cell Lymphoma)
Open Access
Abstract
(1) Background: Monomorphic intestinal epitheliotropic T-cell lymphoma (MEITL) is a very rare subtype of lymphoma, being involved in less than 5% of lymphomas of the digestive tract. Accurate diagnosis is extremely challenging due to the lack of specific clinical symptoms and the low specificity of the diagnostic approaches. (2) Methods: We present the case of a patient admitted to the Neurology Clinic of the Emergency Clinical Hospital of Galati, Romania, with progressive cranial nerve impairment. (3) Results: Analyzing clinical and paraclinical data and corroborating the previous known diagnosis of MEITL, the positive diagnosis was that of meningitis with atypical lymphocytes with MEITL as starting point. The cytology of CSF was the basis for the diagnostic confirmation. (4) Conclusions: The present case is a rare situation of secondary dissemination of MEITL. We were not able to identify a similar report in the available literature that associated urothelial carcinoma with leptomeningeal MEITL-sourced neoplastic lesions.Keywords
Funding Information
- the Faculty of Medicine and Pharmacy “Lower Danube” University of Galati
This publication has 17 references indexed in Scilit:
- Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma:Pathological Phenotype and Genetic Mutation Analysis of 12 PatientsBlood, 2023
- Early central nervous system relapse of monomorphic epitheliotropic intestinal T-cell lymphoma after cord blood transplantationInternational Journal of Hematology, 2021
- Clinicopathologic Determinants of Survival in Monomorphic Epitheliotropic Intestinal T-Cell Lymphoma (MEITL): Analysis of a Pooled DatabaseBlood, 2020
- Whole-genome sequencing reveals potent therapeutic strategy for monomorphic epitheliotropic intestinal T-cell lymphomaBlood Advances, 2020
- Unusual Case of Abdominal Fullness in a Middle-Aged WomanGastroenterology, 2019
- Type II enteropathy-associated T-cell lymphoma features a unique genomic profile with highly recurrent SETD2 alterationsNature Communications, 2016
- Activating mutations of STAT5B and STAT3 in lymphomas derived from γδ-T or NK cellsNature Communications, 2015
- Pathological and immunohistological findings and genetic aberrations of intestinal enteropathy‐associated T cell lymphoma in JapanHistopathology, 2011
- Enteropathy-Associated T Cell Lymphoma With Brain InvolvementJournal of Clinical Gastroenterology, 1998
- 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.Gut, 1997